Gene Scoring 843 total scored genes, 164 uncategorized

Database updated on June 22, 2017

Scoring process

We recognize that the gene scoring process we developed is only one of many methodologies that could have been employed to evaluate these genes. Our goal is to encourage more research, not less, and we hope that researchers will use these evaluations to design new experiments aimed at strengthening the evidence associating each gene with ASD. For more information on our scoring process, visit the About Gene Scoring – Criteria page.

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Score Distribution   Click on a score to refine results

S Category S   [68 genes]

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Status Gene Symbol Gene Name Chromosome Genetic Category Gene Score Syndromic reports
ATP1A3ATPase Na+/K+ transporting subunit alpha 319Rare Single Gene Mutation, Syndromic, Functional4S12
CAMK2Acalcium/calmodulin dependent protein kinase II alpha5Rare Single Gene Mutation, Syndromic, Genetic Association, Functional4S4
CNOT3CCR4-NOT transcription complex subunit 319Rare Single Gene Mutation, Syndromic3S3
ADNPActivity-dependent neuroprotector homeobox20Rare Single Gene Mutation, Syndromic1S23
ARHGEF9Cdc42 guanine nucleotide exchange factor (GEF) 9XRare Single Gene Mutation, Syndromic4S7
ARID1BAT rich interactive domain 1B (SWI1-like)6Rare Single Gene Mutation, Syndromic1S34
DYRK1ADual-specificity tyrosine-(Y)-phosphorylation regulated kinase 1A21Rare Single Gene Mutation, Syndromic1S32
FOXP1forkhead box P13Rare Single Gene Mutation, Syndromic, Genetic Association, Functional2S36
EP300E1A binding protein p30022Rare Single Gene Mutation, Syndromic4S16
DEAF1DEAF1 transcription factor11Rare Single Gene Mutation, Syndromic2S14
EHMT1Euchromatic histone-lysine N-methyltransferase 19Rare Single Gene Mutation, Syndromic3S20
ANKRD11ankyrin repeat domain 1116Rare Single Gene Mutation, Syndromic2S36
CHD1chromodomain helicase DNA binding protein 15Rare Single Gene Mutation4S3
CHD2Chromodomain helicase DNA binding protein 215Rare Single Gene Mutation, Syndromic1S25
DDX3XDEAD (Asp-Glu-Ala-Asp) box helicase 3, X-linkedXRare Single Gene Mutation, Syndromic2S12
ASXL3Additional sex combs like 3 (Drosophila)18Rare Single Gene Mutation, Syndromic1S16
BCL11AB-cell CLL/lymphoma 11A (zinc finger protein)2Rare Single Gene Mutation, Syndromic2S16
CHD8chromodomain helicase DNA binding protein 814Rare Single Gene Mutation1S27
CICcapicua transcriptional repressor19Rare Single Gene Mutation, Functional2S4
CNKSR2connector enhancer of kinase suppressor of Ras 2XSyndromic3S3
CNTNAP2contactin associated protein-like 27Rare Single Gene Mutation, Syndromic, Genetic Association2S58
AHDC1AT-hook DNA binding motif containing 11Rare Single Gene Mutation, Syndromic3S8
IQSEC2IQ motif and Sec7 domain 2XRare Single Gene Mutation, Syndromic4S18
MBOAT7membrane bound O-acyltransferase domain containing 719Rare Single Gene Mutation, Syndromic2S2
MECP2Methyl CpG binding protein 2XRare Single Gene Mutation, Syndromic, Functional2S67
MBD5Methyl-CpG binding domain protein 52Rare Single Gene Mutation, Syndromic3S29
NR2F1nuclear receptor subfamily 2 group F member 15Rare Single Gene Mutation, Syndromic4S10
KAT6AK(lysine) acetyltransferase 6A8Rare Single Gene Mutation, Syndromic3S8
MEF2Cmyocyte enhancer factor 2C5Rare Single Gene Mutation, Syndromic, Genetic Association, Functional4S28
MTORMechanistic target of rapamycin (serine/threonine kinase)1Rare Single Gene Mutation, Syndromic, Functional3S14
KIF5CKinesin family member 5C2Rare Single Gene Mutation, Syndromic4S7
KMT2ALysine (K)-specific methyltransferase 2A11Rare Single Gene Mutation, Syndromic1S15
KMT2CLysine (K)-specific methyltransferase 2C7Rare Single Gene Mutation, Syndromic2S14
MAGEL2MAGE-like 215Rare Single Gene Mutation, Syndromic2S11
MED13LMediator complex subunit 13-like12Rare Single Gene Mutation, Syndromic2S22
PPP2R5DProtein phosphatase 2, regulatory subunit B', delta6Rare Single Gene Mutation, Syndromic4S13
HNRNPUheterogeneous nuclear ribonucleoprotein U1Rare Single Gene Mutation, Syndromic, Functional4S11
PHIPpleckstrin homology domain interacting protein6Rare Single Gene Mutation, Syndromic3S10
POGZPogo transposable element with ZNF domain1Rare Single Gene Mutation, Syndromic1S22
NACC1nucleus accumbens associated 119Rare Single Gene Mutation, Syndromic4S3
NTNG1netrin G11Rare Single Gene Mutation, Syndromic, Genetic Association4S8
PTENphosphatase and tensin homolog (mutated in multiple advanced cancers 1)10Rare Single Gene Mutation, Syndromic1S48
RPS6KA3Ribosomal protein S6 kinase, 90kDa, polypeptide 3XRare Single Gene Mutation, Syndromic4S9
SCN1Asodium channel, voltage-gated, type I, alpha subunit2Rare Single Gene Mutation, Syndromic, Genetic Association3S46
TRIP12Thyroid hormone receptor interactor 122Rare Single Gene Mutation, Syndromic1S14
TSC2tuberous sclerosis 216Rare Single Gene Mutation, Syndromic, Genetic Association3S26
TTNtitin2Rare Single Gene Mutation, Syndromic4S17
SATB2SATB homeobox 22Rare Single Gene Mutation, Syndromic, Genetic Association4S21
STXBP1Syntaxin binding protein 19Rare Single Gene Mutation, Syndromic3S30
TCF4Transcription factor 418Rare Single Gene Mutation, Syndromic, Genetic Association3S36
REREArginine-glutamic acid dipeptide (RE) repeats1Rare Single Gene Mutation, Syndromic, Genetic Association4S6
ZNF462Zinc finger protein 4629Rare Single Gene Mutation, Syndromic4S7
SLC6A1Solute carrier family 6 (neurotransmitter transporter), member 13Rare Single Gene Mutation, Syndromic, Genetic Association2S16
SYNGAP1synaptic Ras GTPase activating protein 16Rare Single Gene Mutation, Syndromic1S43
PTPN11protein tyrosine phosphatase, non-receptor type 1112Rare Single Gene Mutation, Syndromic4S12
SETD5SET domain containing 53Rare Single Gene Mutation, Syndromic1S22
ZBTB20Zinc finger and BTB domain containing 203Rare Single Gene Mutation, Syndromic3S16
PRODHProline dehydrogenase (oxidase) 122Syndromic, Genetic Association3S6
SHANK3SH3 and multiple ankyrin repeat domains 322Rare Single Gene Mutation, Syndromic, Genetic Association, Functional1S65
SIN3ASIN3 transcription regulator family member A15Rare Single Gene Mutation, Syndromic4S6
SYNE1spectrin repeat containing, nuclear envelope 16Rare Single Gene Mutation, Genetic Association4S15
UBE3Aubiquitin protein ligase E3A15Rare Single Gene Mutation, Syndromic, Genetic Association3S26
WACWW domain containing adaptor with coiled-coil10Rare Single Gene Mutation, Syndromic2S14
RNF135Ring finger protein 13517Syndromic, Genetic Association4S2
SETD1BSET domain containing 1B12Rare Single Gene Mutation, Syndromic4S6
UPF3BUPF3 regulator of nonsense transcripts homolog B (yeast)XRare Single Gene Mutation, Syndromic2S12
SMC3structural maintenance of chromosomes 310Rare Single Gene Mutation, Syndromic4S6
UNC13Aunc-13 homolog A19Rare Single Gene Mutation, Syndromic4S5

1 Category 1   [25 genes]

Status Gene Symbol Gene Name Chromosome Genetic Category Gene Score Syndromic reports
ADNPActivity-dependent neuroprotector homeobox20Rare Single Gene Mutation, Syndromic1S23
ARID1BAT rich interactive domain 1B (SWI1-like)6Rare Single Gene Mutation, Syndromic1S34
DYRK1ADual-specificity tyrosine-(Y)-phosphorylation regulated kinase 1A21Rare Single Gene Mutation, Syndromic1S32
CHD2Chromodomain helicase DNA binding protein 215Rare Single Gene Mutation, Syndromic1S25
ASH1LAsh1 (absent, small, or homeotic)-like (Drosophila)1Rare Single Gene Mutation, Syndromic111
ASXL3Additional sex combs like 3 (Drosophila)18Rare Single Gene Mutation, Syndromic1S16
CHD8chromodomain helicase DNA binding protein 814Rare Single Gene Mutation1S27
ANK2Ankyrin 2, neuronal4Rare Single Gene Mutation112
CUL3Cullin 32Rare Single Gene Mutation, Genetic Association114
DSCAMDown syndrome cell adhesion molecule21Rare Single Gene Mutation, Genetic Association17
MYT1LMyelin transcription factor 1-like2Rare Single Gene Mutation, Syndromic, Genetic Association115
KMT2ALysine (K)-specific methyltransferase 2A11Rare Single Gene Mutation, Syndromic1S15
KMT5Blysine methyltransferase 5B11Rare Single Gene Mutation, Syndromic19
GRIN2Bglutamate receptor, inotropic, N-methyl D-apartate 2B12Rare Single Gene Mutation, Syndromic, Genetic Association144
POGZPogo transposable element with ZNF domain1Rare Single Gene Mutation, Syndromic1S22
KATNAL2Katanin p60 subunit A-like 218Rare Single Gene Mutation17
NAA15N(alpha)-acetyltransferase 15, NatA auxiliary subunit4Rare Single Gene Mutation17
PTENphosphatase and tensin homolog (mutated in multiple advanced cancers 1)10Rare Single Gene Mutation, Syndromic1S48
TRIP12Thyroid hormone receptor interactor 122Rare Single Gene Mutation, Syndromic1S14
RELNReelin7Rare Single Gene Mutation, Syndromic, Genetic Association, Functional144
TBR1T-box, brain, 12Rare Single Gene Mutation, Genetic Association120
SCN2Asodium channel, voltage-gated, type II, alpha subunit2Rare Single Gene Mutation, Syndromic149
SYNGAP1synaptic Ras GTPase activating protein 16Rare Single Gene Mutation, Syndromic1S43
SETD5SET domain containing 53Rare Single Gene Mutation, Syndromic1S22
SHANK3SH3 and multiple ankyrin repeat domains 322Rare Single Gene Mutation, Syndromic, Genetic Association, Functional1S65

2 Category 2   [59 genes]

Status Gene Symbol Gene Name Chromosome Genetic Category Gene Score Syndromic reports
FOXP1forkhead box P13Rare Single Gene Mutation, Syndromic, Genetic Association, Functional2S36
BCKDKBranched chain ketoacid dehydrogenase kinase16Rare Single Gene Mutation23
CNTN4contactin 43Rare Single Gene Mutation, Syndromic, Genetic Association220
CACNA1Hcalcium channel, voltage-dependent, alpha 1H subunit16Rare Single Gene Mutation221
DEAF1DEAF1 transcription factor11Rare Single Gene Mutation, Syndromic2S14
ANKRD11ankyrin repeat domain 1116Rare Single Gene Mutation, Syndromic2S36
DDX3XDEAD (Asp-Glu-Ala-Asp) box helicase 3, X-linkedXRare Single Gene Mutation, Syndromic2S12
GABRB3gamma-aminobutyric acid (GABA) A receptor, beta 315Rare Single Gene Mutation, Genetic Association236
BCL11AB-cell CLL/lymphoma 11A (zinc finger protein)2Rare Single Gene Mutation, Syndromic2S16
CICcapicua transcriptional repressor19Rare Single Gene Mutation, Functional2S4
CNTNAP2contactin associated protein-like 27Rare Single Gene Mutation, Syndromic, Genetic Association2S58
BAZ2Bbromodomain adjacent to zinc finger domain 2B2Rare Single Gene Mutation23
CACNA1Dcalcium channel, voltage-dependent, L type, alpha 1D3Rare Single Gene Mutation, Syndromic, Genetic Association, Functional217
CACNA2D3Calcium channel, voltage-dependent, alpha 2/delta subunit 33Rare Single Gene Mutation25
CTNND2Catenin (cadherin-associated protein), delta 25Rare Single Gene Mutation24
DIP2Cdisco interacting protein 2 homolog C10Rare Single Gene Mutation22
ERBINerbb2 interacting protein5Rare Single Gene Mutation25
GIGYF2GRB10 interacting GYF protein 22Rare Single Gene Mutation27
MBOAT7membrane bound O-acyltransferase domain containing 719Rare Single Gene Mutation, Syndromic2S2
MECP2Methyl CpG binding protein 2XRare Single Gene Mutation, Syndromic, Functional2S67
NRXN1neurexin 12Rare Single Gene Mutation, Syndromic, Genetic Association271
KMT2CLysine (K)-specific methyltransferase 2C7Rare Single Gene Mutation, Syndromic2S14
MAGEL2MAGE-like 215Rare Single Gene Mutation, Syndromic2S11
MED13LMediator complex subunit 13-like12Rare Single Gene Mutation, Syndromic2S22
KDM5BLysine (K)-specific demethylase 5B1Rare Single Gene Mutation, Syndromic210
GRIA1glutamate ionotropic receptor AMPA type subunit 15Rare Single Gene Mutation24
GRIP1glutamate receptor interacting protein 112Rare Single Gene Mutation212
ILF2Interleukin enhancer binding factor 21Rare Single Gene Mutation24
INTS6Integrator complex subunit 613Rare Single Gene Mutation24
IRF2BPLInterferon regulatory factor 2 binding protein-like14Rare Single Gene Mutation23
KAT2BK(lysine) acetyltransferase 2B3Rare Single Gene Mutation25
KDM6Alysine demethylase 6AXRare Single Gene Mutation, Syndromic26
MED13mediator complex subunit 1317Rare Single Gene Mutation23
METmet proto-oncogene (hepatocyte growth factor receptor)7Rare Single Gene Mutation, Genetic Association, Functional236
MSNP1ASMoesinpseudogene 1, antisense5Genetic Association, Functional211
NCKAP1NCK-associated protein 12Rare Single Gene Mutation27
NLGN3neuroligin 3XRare Single Gene Mutation232
PHF3PHD finger protein 36Rare Single Gene Mutation22
SHANK2SH3 and multiple ankyrin repeat domains 211Rare Single Gene Mutation, Syndromic, Functional223
SMARCC2SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily c, member 212Rare Single Gene Mutation, Syndromic, Functional28
WDFY3WD repeat and FYVE domain containing 34Rare Single Gene Mutation, Functional211
TRIOTrio Rho guanine nucleotide exchange factor5Rare Single Gene Mutation220
PTCHD1patched domain containing 1XRare Single Gene Mutation, Genetic Association211
USP7Ubiquitin specific peptidase 7 (herpes virus-associated)16Rare Single Gene Mutation, Syndromic26
SCN9Asodium voltage-gated channel alpha subunit 92Rare Single Gene Mutation25
SLC6A1Solute carrier family 6 (neurotransmitter transporter), member 13Rare Single Gene Mutation, Syndromic, Genetic Association2S16
TBL1XR1Transducin (beta)-like 1 X-linked receptor 13Rare Single Gene Mutation, Syndromic215
TCF20Transcription factor 20 (AR1)22Rare Single Gene Mutation28
WACWW domain containing adaptor with coiled-coil10Rare Single Gene Mutation, Syndromic2S14
RANBP17RAN binding protein 175Rare Single Gene Mutation23
RIMS1Regulating synaptic membrane exocytosis 16Rare Single Gene Mutation, Genetic Association24
UPF3BUPF3 regulator of nonsense transcripts homolog B (yeast)XRare Single Gene Mutation, Syndromic2S12
SPASTSpastin2Rare Single Gene Mutation28
SRCAPSnf2 related CREBBP activator protein16Rare Single Gene Mutation25
SRSF11serine and arginine rich splicing factor 111Rare Single Gene Mutation23
TAOK2TAO kinase 216Rare Single Gene Mutation, Functional25
TNRC6BTrinucleotide repeat containing 6B22Rare Single Gene Mutation25
UBN2ubinuclein 27Rare Single Gene Mutation23
USP15ubiquitin specific peptidase 1512Rare Single Gene Mutation23

3 Category 3   [176 genes]

Status Gene Symbol Gene Name Chromosome Genetic Category Gene Score Syndromic reports
ANK3Ankyrin 3, node of Ranvier (ankyrin G)10Rare Single Gene Mutation, Genetic Association323
CELF4CUGBP, Elav-like family member 418Rare Single Gene Mutation, Functional38
CNOT3CCR4-NOT transcription complex subunit 319Rare Single Gene Mutation, Syndromic3S3
CTCFCCCTC-binding factor (zinc finger protein)16Rare Single Gene Mutation, Syndromic, Functional312
CTNNB1Catenin (cadherin-associated protein), beta 1, 88kDa3Rare Single Gene Mutation, Syndromic320
CTTNBP2cortactin binding protein 27Rare Single Gene Mutation, Syndromic36
DISC1disrupted in schizophrenia 11Rare Single Gene Mutation, Syndromic, Genetic Association332
FBN1Fibrillin 115Rare Single Gene Mutation39
AVPR1Aarginine vasopressin receptor 1A12Rare Single Gene Mutation, Genetic Association321
ASTN2astrotactin 29Rare Single Gene Mutation, Genetic Association312
FOXP2forkhead box P27Rare Single Gene Mutation, Genetic Association338
CNTN5Contactin 511Rare Single Gene Mutation, Genetic Association39
CNTN6Contactin 63Rare Single Gene Mutation, Genetic Association311
CC2D1ACoiled-coil and C2 domain containing 1A19Rare Single Gene Mutation, Functional39
DYNC1H1dynein cytoplasmic 1 heavy chain 114Rare Single Gene Mutation, Syndromic312
EHMT1Euchromatic histone-lysine N-methyltransferase 19Rare Single Gene Mutation, Syndromic3S20
CYFIP1cytoplasmic FMR1 interacting protein 115Rare Single Gene Mutation, Genetic Association314
ELP4Elongator acetyltransferase complex subunit 411Rare Single Gene Mutation, Genetic Association35
AUTS2autism susceptibility candidate 27Rare Single Gene Mutation, Syndromic, Genetic Association332
CACNB2Calcium channel, voltage-dependent, beta 2 subunit10Rare Single Gene Mutation, Genetic Association34
CHRNA7cholinergic receptor, nicotinic, alpha 715Rare Single Gene Mutation313
CNKSR2connector enhancer of kinase suppressor of Ras 2XSyndromic3S3
CNR1cannabinoid receptor 1 (brain)6Rare Single Gene Mutation, Genetic Association37
ACHEAcetylcholinesterase (Yt blood group)7Rare Single Gene Mutation34
ADAadenosine deaminase20Rare Single Gene Mutation, Genetic Association36
ADCY3adenylate cyclase 32Rare Single Gene Mutation32
AGAP2ArfGAP with GTPase domain, ankyrin repeat and PH domain 212Rare Single Gene Mutation33
AHDC1AT-hook DNA binding motif containing 11Rare Single Gene Mutation, Syndromic3S8
AKAP9A kinase (PRKA) anchor protein 97Rare Single Gene Mutation34
AMPD1Adenosine monophosphate deaminase 11Rare Single Gene Mutation, Genetic Association33
AMTAminomethyltransferase3Rare Single Gene Mutation31
ANXA1Annexin A19Rare Single Gene Mutation32
APH1AAPH1A gamma secretase subunit1Rare Single Gene Mutation32
ASPMabnormal spindle microtubule assembly1Rare Single Gene Mutation, Syndromic35
ATP10AProbable phospholipid-transporting ATPase VA15Rare Single Gene Mutation, Genetic Association, Functional37
ATP2B2ATPase, Ca++ transporting, plasma membrane 23Rare Single Gene Mutation, Genetic Association39
CNTNAP4Contactin associated protein-like 416Rare Single Gene Mutation, Functional311
CACNA1Ecalcium voltage-gated channel subunit alpha1 E1Rare Single Gene Mutation38
CAPRIN1Cell cycle associated protein 111Rare Single Gene Mutation, Functional33
CCT4Chaperonin containing TCP1, subunit 4 (delta)2Rare Single Gene Mutation33
CDC42BPBCDC42 binding protein kinase beta (DMPK-like)14Rare Single Gene Mutation36
CEP135centrosomal protein 1354Rare Single Gene Mutation, Syndromic36
CEP41testis specific, 147Rare Single Gene Mutation33
CGNL1Cingulin-like 115Rare Single Gene Mutation33
CHMP1Acharged multivesicular body protein 1A16Rare Single Gene Mutation, Syndromic35
CIB2Calcium and integrin binding family member 215Rare Single Gene Mutation31
CLASP1cytoplasmic linker associated protein 12Rare Single Gene Mutation33
CUL7Cullin 76Rare Single Gene Mutation33
CUX1cut like homeobox 17Rare Single Gene Mutation, Functional33
DAPP1Dual adaptor of phosphotyrosine and 3-phosphoinositides4Rare Single Gene Mutation31
DENRdensity-regulated protein12Rare Single Gene Mutation32
DIP2ADIP2 disco-interacting protein 2 homolog A (Drosophila)21Rare Single Gene Mutation34
DLGAP1DLG associated protein 118Rare Single Gene Mutation, Functional36
DNMT3ADNA (cytosine-5-)-methyltransferase 3 alpha2Rare Single Gene Mutation37
DOCK8dedicator of cytokinesis 89Rare Single Gene Mutation36
DPP10Dipeptidyl-peptidase 102Rare Single Gene Mutation311
DPYSL2dihydropyrimidinase like 28Rare Single Gene Mutation, Genetic Association311
EFR3AEFR3 homolog A (S. cerevisiae)8Rare Single Gene Mutation35
ELAVL3ELAV like neuron-specific RNA binding protein 319Rare Single Gene Mutation33
EP400E1A binding protein p40012Rare Single Gene Mutation36
EMSYEMSY, BRCA2 interacting transcriptional repressor11Rare Single Gene Mutation, Functional33
ETFBElectron-transfer-flavoprotein, beta polypeptide19Rare Single Gene Mutation33
FAM92BFamily with sequence similarity 92, member B16Rare Single Gene Mutation33
GGNBP2gametogenetin binding protein 217Rare Single Gene Mutation32
GIGYF1GRB10 interacting GYF protein 17Rare Single Gene Mutation33
GRIN1Glutamate receptor, ionotropic, N-methyl D-aspartate 19Rare Single Gene Mutation, Functional314
KCNQ2Potassium voltage-gated channel, KQT-like subfamily, member 220Rare Single Gene Mutation, Syndromic, Genetic Association318
KCNQ3Potassium voltage-gated channel, KQT-like subfamily, member 38Rare Single Gene Mutation, Genetic Association37
MACROD2MACRO domain containing 220Rare Single Gene Mutation, Genetic Association317
ITGB3integrin, beta 3 (platelet glycoprotein IIIa, antigen CD61)17Rare Single Gene Mutation, Genetic Association314
MBD5Methyl-CpG binding domain protein 52Rare Single Gene Mutation, Syndromic3S29
NLGN4Xneuroligin 4, X-linkedXRare Single Gene Mutation, Genetic Association329
NRXN3neurexin 314Rare Single Gene Mutation, Genetic Association316
OPHN1oligophrenin 1XRare Single Gene Mutation, Syndromic312
OXTRoxytocin receptor3Rare Single Gene Mutation, Genetic Association, Functional342
GRIK2glutamate receptor, ionotropic, kainate 26Rare Single Gene Mutation, Genetic Association317
KAT6AK(lysine) acetyltransferase 6A8Rare Single Gene Mutation, Syndromic3S8
KDM6BLysine (K)-specific demethylase 6B17Rare Single Gene Mutation38
MTORMechanistic target of rapamycin (serine/threonine kinase)1Rare Single Gene Mutation, Syndromic, Functional3S14
NLGN1neuroligin 13Rare Single Gene Mutation, Genetic Association317
GPHNGephyrin14Rare Single Gene Mutation38
JARID2jumonji and AT-rich interaction domain containing 26Rare Single Gene Mutation, Syndromic, Genetic Association311
PAHPhenylalanine hydroxylase12Rare Single Gene Mutation, Syndromic32
PLCB1phospholipase C, beta 1 (phosphoinositide-specific)20Rare Single Gene Mutation37
PRICKLE1Prickle homolog 1 (Drosophila)12Rare Single Gene Mutation, Syndromic, Functional34
PRICKLE2Prickle homolog 2 (Drosophila)3Rare Single Gene Mutation, Functional33
NEXMIFneurite extension and migration factorXRare Single Gene Mutation, Syndromic316
HECW2HECT, C2 and WW domain containing E3 ubiquitin protein ligase 22Rare Single Gene Mutation, Syndromic36
KDM5CLysine (K)-specific demethylase 5CXRare Single Gene Mutation, Syndromic320
GPC4glypican 4XRare Single Gene Mutation32
GRID1Glutamate receptor, ionotropic, delta 110Rare Single Gene Mutation, Genetic Association36
GRIK5Glutamate receptor, ionotropic, kainate 519Rare Single Gene Mutation36
PHIPpleckstrin homology domain interacting protein6Rare Single Gene Mutation, Syndromic3S10
HECTD4HECT domain E3 ubiquitin protein ligase 412Rare Single Gene Mutation33
HIVEP3human immunodeficiency virus type I enhancer binding protein 31Rare Single Gene Mutation, Genetic Association34
KCNJ10Potassium inwardly-rectifying channel, subfamily J, member 101Rare Single Gene Mutation, Syndromic, Genetic Association310
HMGN1high mobility group nucleosome binding domain 121Genetic Association31
KIAA1586KIAA15866Rare Single Gene Mutation33
KIRREL3Kin of IRRE like 3 (Drosophila)11Rare Single Gene Mutation313
KMT2ELysine (K)-specific methyltransferase 2E7Rare Single Gene Mutation33
LAMB1laminin, beta 17Rare Single Gene Mutation, Genetic Association35
LMX1BLIM homeobox transcription factor 1, beta9Genetic Association31
LZTR1Leucine-zipper-like transcription regulator 122Rare Single Gene Mutation33
MFRPMembrane frizzled-related protein11Rare Single Gene Mutation35
MYO5Amyosin VA15Rare Single Gene Mutation, Genetic Association34
MYO9BMyosin IXB19Rare Single Gene Mutation32
NAV2neuron navigator 211Rare Single Gene Mutation38
NINLNinein-like20Rare Single Gene Mutation33
NR3C2Nuclear receptor subfamily 3, group C, member 24Rare Single Gene Mutation33
NUAK1NUAK family, SNF1-like kinase, 112Rare Single Gene Mutation35
OR52M1Olfactory receptor, family 52, subfamily M, member 111Rare Single Gene Mutation32
OTUD7AOTU deubiquitinase 7A15Functional33
P2RX5Purinergic receptor P2X, ligand gated ion channel, 517Rare Single Gene Mutation32
P4HA2Prolyl 4-hydroxylase, alpha polypeptide II5Rare Single Gene Mutation34
PARD3BPar-3 partitioning defective 3 homolog B (C. elegans)2Rare Single Gene Mutation, Genetic Association36
PAX5Paired box 59Rare Single Gene Mutation34
PER2period circadian clock 22Rare Single Gene Mutation32
PHBprohibitin17Genetic Association31
PHF2PHD finger protein 29Rare Single Gene Mutation35
PHRF1PHD and ring finger domains 111Rare Single Gene Mutation34
PLXNA4Plexin A47Rare Single Gene Mutation, Functional34
PLXNB1plexin B13Rare Single Gene Mutation33
PON1paraoxonase 17Genetic Association35
PREX1Phosphatidylinositol-3,4,5-trisphosphate-dependent Rac exchange factor 120Genetic Association31
PRKCBprotein kinase C, beta16Rare Single Gene Mutation, Genetic Association36
SBF1SET binding factor 122Rare Single Gene Mutation36
SCN1Asodium channel, voltage-gated, type I, alpha subunit2Rare Single Gene Mutation, Syndromic, Genetic Association3S46
TRAPPC9trafficking protein particle complex 98Rare Single Gene Mutation, Syndromic311
SCN8Asodium channel, voltage gated, type VIII, alpha subunit12Rare Single Gene Mutation, Syndromic326
SETBP1SET binding protein 118Rare Single Gene Mutation, Syndromic310
TSC2tuberous sclerosis 216Rare Single Gene Mutation, Syndromic, Genetic Association3S26
SEMA5Asema domain, seven thrombospondin repeats (type 1 and type 1-like), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 5A5Rare Single Gene Mutation, Genetic Association, Functional316
SLC12A5Solute carrier family 12 (potassium/chloride transporter), member 520Rare Single Gene Mutation35
ZMYND11Zinc finger, MYND-type containing 1110Rare Single Gene Mutation, Syndromic310
STXBP1Syntaxin binding protein 19Rare Single Gene Mutation, Syndromic3S30
TCF4Transcription factor 418Rare Single Gene Mutation, Syndromic, Genetic Association3S36
PRKNparkin RBR E3 ubiquitin protein ligase6Rare Single Gene Mutation, Genetic Association314
SMARCA4SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 419Rare Single Gene Mutation, Syndromic36
RBFOX1RNA binding protein, fox-1 homolog (C. elegans) 116Rare Single Gene Mutation, Genetic Association332
SETD2SET domain containing 23Rare Single Gene Mutation39
ZBTB20Zinc finger and BTB domain containing 203Rare Single Gene Mutation, Syndromic3S16
PRODHProline dehydrogenase (oxidase) 122Syndromic, Genetic Association3S6
ROBO2Roundabout, axon guidance receptor, homolog 2 (Drosophila)3Rare Single Gene Mutation, Genetic Association, Functional38
TMLHEtrimethyllysine hydroxylase, epsilonXRare Single Gene Mutation, Genetic Association35
UBE3Aubiquitin protein ligase E3A15Rare Single Gene Mutation, Syndromic, Genetic Association3S26
PTK7Protein tyrosine kinase 7 (inactive)6Rare Single Gene Mutation34
PYHIN1Pyrin and HIN domain family, member 11Rare Single Gene Mutation34
RAB2ARAB2A, member RAS oncogene family8Rare Single Gene Mutation38
RAB43RAB43, member RAS oncogene family3Rare Single Gene Mutation32
RBM27RNA binding motif protein 275Rare Single Gene Mutation32
WWOXWW domain containing oxidoreductase16Rare Single Gene Mutation, Syndromic38
ZNF804AZinc finger protein 804A2Rare Single Gene Mutation, Genetic Association311
SAE1SUMO1 activating enzyme subunit 119Rare Single Gene Mutation33
SHANK1SH3 and multiple ankyrin repeat domains 119Rare Single Gene Mutation35
SHOXshort stature homeoboxX,YRare Single Gene Mutation32
SLC35B1solute carrier family 35 member B117Genetic Association31
SLC38A10solute carrier family 38, member 1017Rare Single Gene Mutation31
SLC6A3Solute carrier family 6 (neurotransmitter transporter), member 35Rare Single Gene Mutation, Genetic Association311
SLC7A3Solute carrier family 7 (cationic amino acid transporter, y+ system), member 3XRare Single Gene Mutation32
SLC7A5solute carrier family 7 member 516Functional31
SMAD4SMAD family member 418Rare Single Gene Mutation33
SPARCL1SPARC like 14Rare Single Gene Mutation, Functional33
STXBP5Syntaxin binding protein 5 (tomosyn)6Rare Single Gene Mutation36
TAF6TATA-box binding protein associated factor 67Rare Single Gene Mutation32
TBC1D31TBC1 domain family, member 318Rare Single Gene Mutation33
TCF7L2Transcription factor 7-like 2 (T-cell specific, HMG-box)10Rare Single Gene Mutation32
TERF2Telomeric repeat binding factor 216Rare Single Gene Mutation33
TET2Tet methylcytosine dioxygenase 24Rare Single Gene Mutation34
TRPC6Transient receptor potential cation channel, subfamily C, member 611Rare Single Gene Mutation32
TRPM1Transient receptor potential cation channel, subfamily M, member 115Rare Single Gene Mutation33
UBE3CUbiquitin protein ligase E3C7Rare Single Gene Mutation34
UBR5Ubiquitin protein ligase E3 component n-recognin 58Rare Single Gene Mutation36
UNC79unc-79 homolog, NALCN channel complex subunit14Rare Single Gene Mutation32
USP45Ubiquitin specific peptidase 456Rare Single Gene Mutation32
VIL1Villin 12Rare Single Gene Mutation31
ZC3H4zinc finger CCCH-type containing 419Rare Single Gene Mutation33

4 Category 4   [405 genes]

Status Gene Symbol Gene Name Chromosome Genetic Category Gene Score Syndromic reports
ARNT2aryl-hydrocarbon receptor nuclear translocator 215Rare Single Gene Mutation, Syndromic, Genetic Association411
ATP1A3ATPase Na+/K+ transporting subunit alpha 319Rare Single Gene Mutation, Syndromic, Functional4S12
ATRXalpha thalassemia/mental retardation syndrome X-linkedXRare Single Gene Mutation, Syndromic417
CADPS2Ca2+-dependent activator protein for secretion 27Rare Single Gene Mutation, Functional412
CAMK2Acalcium/calmodulin dependent protein kinase II alpha5Rare Single Gene Mutation, Syndromic, Genetic Association, Functional4S4
CYP11B1cytochrome P450, family 11, subfamily B, polypeptide 18Syndromic44
ARHGEF9Cdc42 guanine nucleotide exchange factor (GEF) 9XRare Single Gene Mutation, Syndromic4S7
CSMD1CUB and Sushi multiple domains 18Rare Single Gene Mutation, Genetic Association411
DIXDC1DIX domain containing 111Rare Single Gene Mutation, Functional44
EXT1Exostosin 18Rare Single Gene Mutation, Genetic Association46
ADORA2Aadenosine A2a receptor22Syndromic47
ASMTacetylserotonin O-methyltransferaseX,YRare Single Gene Mutation, Genetic Association49
CADM1cell adhesion molecule 111Rare Single Gene Mutation48
DDX53DEAD (Asp-Glu-Ala-Asp) box polypeptide 53XRare Single Gene Mutation43
ADCY5Adenylate cyclase 53Rare Single Gene Mutation46
AFF2AF4/FMR2 family, member 2XRare Single Gene Mutation, Syndromic414
AGBL4ATP/GTP binding protein-like 41Rare Single Gene Mutation43
ARHGAP32Rho GTPase activating protein 3211Rare Single Gene Mutation, Functional44
BRCA2breast cancer 2, early onset13Rare Single Gene Mutation43
BRD4bromodomain containing 419Rare Single Gene Mutation, Syndromic44
BST1bone marrow stromal cell antigen 14Genetic Association, Functional45
EP300E1A binding protein p30022Rare Single Gene Mutation, Syndromic4S16
FABP5fatty acid binding protein 5 (psoriasis-associated)8Rare Single Gene Mutation, Functional46
CD38CD38 molecule4Genetic Association, Functional47
CMIPc-Maf inducing protein16Rare Single Gene Mutation, Genetic Association46
CTNNA3catenin (cadherin-associated protein), alpha 310Rare Single Gene Mutation, Genetic Association414
ESR2estrogen receptor 2 (ER beta)14Rare Single Gene Mutation, Syndromic47
FAN1FANCD2/FANCI-associated nuclease 115Rare Single Gene Mutation41
CDH11cadherin 1116Rare Single Gene Mutation43
CHD1chromodomain helicase DNA binding protein 15Rare Single Gene Mutation4S3
DPP6dipeptidyl-peptidase 67Rare Single Gene Mutation, Genetic Association, Functional423
DRD3dopamine receptor D33Rare Single Gene Mutation, Genetic Association48
GNASGNAS complex locus20Rare Single Gene Mutation48
CASKcalcium/calmodulin dependent serine protein kinaseXRare Single Gene Mutation, Syndromic412
ABCA10ATP-binding cassette, sub-family A (ABC1), member 1017Rare Single Gene Mutation41
ABCA13ATP binding cassette subfamily A member 137Rare Single Gene Mutation, Functional45
ABCA7ATP-binding cassette, sub-family A (ABC1), member 719Rare Single Gene Mutation42
ACEangiotensin I converting enzyme17Rare Single Gene Mutation, Genetic Association42
ADKadenosine kinase10Rare Single Gene Mutation42
ADORA3Adenosine A3 receptor1Rare Single Gene Mutation, Functional42
ADRB2adrenergic, beta-2-, receptor, surface5Genetic Association410
AGAP1ArfGAP with GTPase domain, ankyrin repeat and PH domain 12Rare Single Gene Mutation48
AGMOalkylglycerol monooxygenase7Rare Single Gene Mutation, Genetic Association45
AGO1argonaute 1, RISC catalytic component1Rare Single Gene Mutation42
AGTR2angiotensin II receptor, type 2XRare Single Gene Mutation43
APBA2amyloid beta (A4) precursor protein-binding, family A, member 215Rare Single Gene Mutation46
ARandrogen receptorXGenetic Association46
ARHGAP5Rho GTPase activating protein 514Rare Single Gene Mutation43
ARHGEF10Rho guanine nucleotide exchange factor 108Rare Single Gene Mutation, Functional43
ATP6V0A2ATPase H+ transporting V0 subunit a212Rare Single Gene Mutation42
AVPR1Barginine vasopressin receptor 1B1Genetic Association, Functional48
AZGP1alpha-2-glycoprotein 1, zinc-binding7Rare Single Gene Mutation42
BBS4Bardet-Biedl syndrome 415Rare Single Gene Mutation, Syndromic43
BIRC6Baculoviral IAP repeat containing 62Rare Single Gene Mutation47
CNTNAP5contactin associated protein-like 52Rare Single Gene Mutation, Genetic Association411
EXOC6Bexocyst complex component 6B2Rare Single Gene Mutation43
BICDL1BICD family like cargo adaptor 112Genetic Association42
C15orf62chromosome 15 open reading frame 6215Rare Single Gene Mutation42
C3orf58chromosome 3 open reading frame 583Rare Single Gene Mutation43
C4Bcomplement component 4B6Genetic Association, Functional45
CA6carbonic anhydrase VI1Rare Single Gene Mutation46
CACNA1Fcalcium channel, voltage-dependent, alpha 1FXRare Single Gene Mutation, Genetic Association47
CACNA1Gcalcium channel, voltage-dependent, T type, alpha 1G subunit17Rare Single Gene Mutation, Genetic Association418
CACNA1ICalcium channel, voltage-dependent, T type, alpha 1I subunit22Rare Single Gene Mutation, Genetic Association46
CADM2Cell adhesion molecule 23Genetic Association43
CAMK4Calcium/calmodulin-dependent protein kinase IV5Genetic Association41
CAPN12Calpain 1219Rare Single Gene Mutation44
CARD11caspase recruitment domain family member 117Rare Single Gene Mutation41
CASC4cancer susceptibility candidate 415Rare Single Gene Mutation44
CCDC88CCoiled-coil domain containing 88C14Rare Single Gene Mutation45
CCDC91coiled-coil domain containing 9112Rare Single Gene Mutation43
CD276CD276molecule15Rare Single Gene Mutation41
CD99L2CD99 molecule-like 2XGenetic Association41
CDH10cadherin 10, type 2 (T2-cadherin)5Rare Single Gene Mutation, Genetic Association49
CDH22cadherin-like 2220Genetic Association44
CDH8cadherin 8, type 216Rare Single Gene Mutation49
CDH9cadherin 9, type 2 (T1-cadherin)5Rare Single Gene Mutation, Genetic Association46
CECR2CECR2, histone acetyl-lysine reader22Rare Single Gene Mutation42
CELF6CUGBP, Elav-like family member 615Rare Single Gene Mutation, Genetic Association42
CHRM3Cholinergic receptor, muscarinic 31Rare Single Gene Mutation, Genetic Association45
CHRNB3cholinergic receptor nicotinic beta 3 subunit8Rare Single Gene Mutation41
CLN8Ceroid-lipofuscinosis, neuronal 8 (epilepsy, progressive with mental retardation)8Rare Single Gene Mutation, Syndromic43
CLTCL1clathrin, heavy chain-like 122Rare Single Gene Mutation45
CNGB3cyclic nucleotide gated channel beta 38Rare Single Gene Mutation42
COL28A1collagen type XXVIII alpha 1 chain7Rare Single Gene Mutation42
CPT2carnitine palmitoyltransferase 21Rare Single Gene Mutation42
CSNK1Ecasein kinase 1 epsilon22Rare Single Gene Mutation, Functional45
CX3CR1Chemokine (C-X3-C motif) receptor 13Rare Single Gene Mutation, Functional43
CYLC2cylicin, basic protein of sperm head cytoskeleton 29Rare Single Gene Mutation43
DAGLADiacylglycerol lipase, alpha11Rare Single Gene Mutation, Functional44
DDCdopa decarboxylase7Genetic Association42
DLG1discs large MAGUK scaffold protein 13Rare Single Gene Mutation43
DLGAP2discs, large (Drosophila) homolog-associated protein 28Rare Single Gene Mutation412
DLX2distal-less homeobox 22Genetic Association411
DLX6distal-less homeobox 67Rare Single Gene Mutation49
DMXL2Dmx-like 215Rare Single Gene Mutation43
DNAH10Dynein, axonemal, heavy chain 1012Rare Single Gene Mutation45
DNAH17dynein axonemal heavy chain 1717Rare Single Gene Mutation44
DNAH3dynein axonemal heavy chain 316Rare Single Gene Mutation43
DNERDelta/notch-like EGF repeat containing2Rare Single Gene Mutation, Genetic Association42
DOCK1Dedicator of cytokinesis 110Rare Single Gene Mutation42
DOCK4Dedicator of cytokinesis 47Rare Single Gene Mutation, Genetic Association48
DPP4Dipeptidyl-peptidase 42Rare Single Gene Mutation, Genetic Association46
DPYDdihydropyrimidine dehydrogenase1Rare Single Gene Mutation, Genetic Association49
DPYSL3dihydropyrimidinase like 35Rare Single Gene Mutation42
DRD1Dopamine receptor D15Genetic Association, Functional44
DRD2Dopamine receptor D211Rare Single Gene Mutation, Genetic Association46
DSTDystonin6Rare Single Gene Mutation44
DUSP15dual specificity phosphatase 1520Rare Single Gene Mutation, Genetic Association43
DVL3Dishevelled segment polarity protein 33Rare Single Gene Mutation, Functional43
DYDC1DPY30 domain containing 11041
DYDC2DPY30 domain containing 21041
EIF3Geukaryotic translation initiation factor 3 subunit G19Rare Single Gene Mutation43
EIF4Eeukaryotic translation initiation factor 4E4Rare Single Gene Mutation, Genetic Association412
ELAVL2ELAV like neuron-specific RNA binding protein 29Rare Single Gene Mutation, Genetic Association, Functional45
EN2engrailed homolog 27Rare Single Gene Mutation, Genetic Association, Functional420
EPC2Enhancer of polycomb homolog 2 (Drosophila)2Rare Single Gene Mutation44
EPHB2EPH receptor B21Rare Single Gene Mutation43
EPPK1epiplakin 18Rare Single Gene Mutation43
ERGv-ets erythroblastosis virus E26 oncogene homolog (avian)21Genetic Association41
ERMNermin2Rare Single Gene Mutation41
ESRRBestrogen-related receptor beta14Rare Single Gene Mutation, Genetic Association47
FAM47Afamily with sequence similarity 47 member AXRare Single Gene Mutation41
FAT1FAT atypical cadherin 14Rare Single Gene Mutation44
FBXO33F-box protein 3314Genetic Association43
FBXO40F-box protein 403Rare Single Gene Mutation, Genetic Association44
FCRL6Fc receptor like 61Rare Single Gene Mutation44
FEZF2FEZ family zinc finger 23Rare Single Gene Mutation, Genetic Association48
FGAFibrinogen alpha chain4Genetic Association41
FHITfragile histidine triad gene3Rare Single Gene Mutation, Genetic Association412
FRKfyn-related kinase6Rare Single Gene Mutation, Genetic Association43
GABRA4gamma-aminobutyric acid (GABA) A receptor, alpha 44Rare Single Gene Mutation, Genetic Association46
GALNT13UDP-N-acetyl-alpha-D-galactosamine:polypeptide N-acetylgalactosaminyltransferase 13 (GalNAc-T13)2Rare Single Gene Mutation44
GALNT14UDP-N-acetyl-alpha-D-galactosamine:polypeptide N-acetylgalactosaminyltransferase 14 (GalNAc-T14)2Rare Single Gene Mutation, Genetic Association44
GAS2Growth arrest-specific 211Genetic Association41
GDAGuanine deaminase9Rare Single Gene Mutation, Genetic Association42
GLIS1GLIS family zinc finger 11Rare Single Gene Mutation, Genetic Association42
GLO1glyoxalase I6Genetic Association49
IL1RAPL1interleukin 1 receptor accessory protein-like 1XRare Single Gene Mutation420
IQSEC2IQ motif and Sec7 domain 2XRare Single Gene Mutation, Syndromic4S18
KCNMA1potassium large conductance calcium-activated channel, subfamily M, alpha member 110Rare Single Gene Mutation418
NIPA1non imprinted in Prader-Willi/Angelman syndrome 115Rare Single Gene Mutation45
HSD11B1hydroxysteroid (11-beta) dehydrogenase 11Syndromic48
IMMP2LIMP2 inner mitochondrial membrane peptidase-like (S. cerevisiae)7Rare Single Gene Mutation, Genetic Association412
NIPA2non imprinted in Prader-Willi/Angelman syndrome 215Rare Single Gene Mutation42
NR2F1nuclear receptor subfamily 2 group F member 15Rare Single Gene Mutation, Syndromic4S10
PIK3CGphosphoinositide-3-kinase, catalytic, gamma polypeptide7Genetic Association44
PRKDCprotein kinase, DNA-activated, catalytic polypeptide8Rare Single Gene Mutation, Syndromic, Functional44
NRXN2neurexin 211Rare Single Gene Mutation, Genetic Association48
ICA1islet cell autoantigen 1, 69kDa7Rare Single Gene Mutation44
KCND2Potassium voltage-gated channel, Shal-related subfamily, member 27Rare Single Gene Mutation, Genetic Association44
KCND3potassium voltage-gated channel subfamily D member 31Rare Single Gene Mutation, Syndromic, Genetic Association48
KHDRBS2KH domain containing, RNA binding, signal transduction associated 26Rare Single Gene Mutation42
MAOAmonoamine oxidase AXRare Single Gene Mutation, Syndromic, Genetic Association414
MEF2Cmyocyte enhancer factor 2C5Rare Single Gene Mutation, Syndromic, Genetic Association, Functional4S28
NLGN2Neuroligin 217Rare Single Gene Mutation, Functional46
NXPH1neurexophilin 17Rare Single Gene Mutation45
OXToxytocin/neurophysin I prepropeptide20Genetic Association44
HRASv-Ha-ras Harvey rat sarcoma viral oncogene homolog11Rare Single Gene Mutation, Syndromic, Genetic Association411
JMJD1Cjumonji domain containing 1C10Rare Single Gene Mutation47
KIF5CKinesin family member 5C2Rare Single Gene Mutation, Syndromic4S7
LRP2Low density lipoprotein receptor-related protein 22Rare Single Gene Mutation, Syndromic, Genetic Association411
PPP2R5DProtein phosphatase 2, regulatory subunit B', delta6Rare Single Gene Mutation, Syndromic4S13
HDLBPhigh density lipoprotein binding protein2Rare Single Gene Mutation44
HNRNPH2heterogeneous nuclear ribonucleoprotein H2 (H')XRare Single Gene Mutation45
HNRNPUheterogeneous nuclear ribonucleoprotein U1Rare Single Gene Mutation, Syndromic, Functional4S11
ITPR1inositol 1,4,5-trisphosphate receptor type 13Rare Single Gene Mutation48
LRFN5leucine rich repeat and fibronectin type III domain containing 514Rare Single Gene Mutation, Genetic Association46
MTF1metal-regulatory transcription factor 11Syndromic, Genetic Association44
MTHFRmethylenetetrahydrofolate reductase (NAD(P)H)1Rare Single Gene Mutation, Syndromic, Genetic Association415
NTRK1neurotrophic tyrosine kinase, receptor, type 11Rare Single Gene Mutation, Syndromic48
GNB1Lguanine nucleotide binding protein (G protein), beta polypeptide 1-like22Rare Single Gene Mutation, Genetic Association42
GPC6glypican 613Rare Single Gene Mutation, Genetic Association48
GPR37G protein-coupled receptor 37 (endothelin receptor type B-like)7Rare Single Gene Mutation42
GPR85G protein-coupled receptor 857Rare Single Gene Mutation, Genetic Association44
GPX1glutathione peroxidase 13Genetic Association45
GRID2glutamate receptor, ionotropic, delta 24Rare Single Gene Mutation, Syndromic, Genetic Association49
GRIN2Aglutamate receptor, ionotropic, N-methyl D-aspartate 2A16Rare Single Gene Mutation, Syndromic, Genetic Association434
NTRK3neurotrophic tyrosine kinase, receptor, type 315Rare Single Gene Mutation, Syndromic, Genetic Association413
GRM5Glutamate receptor, metabotropic 511Rare Single Gene Mutation, Genetic Association, Functional45
GRM7Glutamate receptor, metabotropic 73Rare Single Gene Mutation, Genetic Association413
GSTM1glutathione S-transferase M11Genetic Association43
GTF2Igeneral transcription factor IIi7Rare Single Gene Mutation, Genetic Association45
GUCY1A2Guanylate cyclase 1, soluble, alpha 211Rare Single Gene Mutation, Genetic Association42
MDGA2MAM domain containing glycosylphosphatidylinositol anchor 214Rare Single Gene Mutation, Genetic Association47
NACC1nucleus accumbens associated 119Rare Single Gene Mutation, Syndromic4S3
NFIAnuclear factor I/A1Rare Single Gene Mutation48
HLA-Amajor histocompatibility complex, class I, A6Genetic Association48
HLA-BMajor histocompatibility complex, class I, B6Genetic Association43
HLA-Gmajor histocompatibility complex, class I, G6Genetic Association43
HOMER1Homer homolog 1 (Drosophila)5Rare Single Gene Mutation, Functional45
HS3ST5heparan sulfate (glucosamine) 3-O-sulfotransferase 56Genetic Association47
HTR1B5-hydroxytryptamine (serotonin) receptor 1B6Rare Single Gene Mutation, Genetic Association46
HTR3A5-hydroxytryptamine (serotonin) receptor 3A11Rare Single Gene Mutation, Genetic Association, Functional47
HTR3C5-hydroxytryptamine (serotonin) receptor 3, family member C3Rare Single Gene Mutation, Genetic Association45
HYDINHYDIN, axonemal central pair apparatus protein16Rare Single Gene Mutation, Genetic Association43
IL1R2interleukin 1 receptor, type II2Rare Single Gene Mutation46
IL1RAPL2interleukin 1 receptor accessory protein-like 2XRare Single Gene Mutation, Genetic Association42
PCDH9protocadherin 913Rare Single Gene Mutation, Genetic Association47
INPP1inositol polyphosphate-1-phosphatase2Rare Single Gene Mutation, Genetic Association44
IQGAP3IQ motif containing GTPase activating protein 31Rare Single Gene Mutation42
KATNAL1katanin catalytic subunit A1 like 113Rare Single Gene Mutation, Functional42
KCNK7potassium two pore domain channel subfamily K member 711Rare Single Gene Mutation41
KCTD13Potassium channel tetramerisation domain containing 1316Rare Single Gene Mutation46
KDM4Blysine demethylase 4B19Rare Single Gene Mutation, Functional43
KIF13BKinesin family member 13B8Rare Single Gene Mutation43
KLF16Kruppel like factor 1619Rare Single Gene Mutation41
KRR1KRR1, small subunit (SSU) processome component, homolog (yeast)12Genetic Association41
KRT26keratin 2617Rare Single Gene Mutation42
LAMA1Laminin, alpha 118Rare Single Gene Mutation, Genetic Association45
LEPLeptin7Rare Single Gene Mutation41
LILRB2leukocyte immunoglobulin like receptor B219Rare Single Gene Mutation42
LIN7Blin-7 homolog B, crumbs cell polarity complex component1941
LRBALPS-responsive vesicle trafficking, beach and anchor containing4Rare Single Gene Mutation45
LRFN2leucine rich repeat and fibronectin type III domain containing 26Rare Single Gene Mutation, Genetic Association, Functional44
LRRC1leucine rich repeat containing 16Genetic Association45
LZTS2leucine zipper, putative tumor suppressor 210Genetic Association44
MAPK3mitogen-activated protein kinase 316Rare Single Gene Mutation43
MARK1MAP/microtubule affinity-regulating kinase 11Rare Single Gene Mutation, Genetic Association410
MBD1methyl-CpG binding domain protein 118Rare Single Gene Mutation47
MBD3methyl-CpG binding domain protein 319Rare Single Gene Mutation44
MBD4methyl-CpG binding domain protein 43Rare Single Gene Mutation46
MBD6Methyl-CpG binding domain protein 612Rare Single Gene Mutation41
MCM4minichromosome maintenance complex component 48Rare Single Gene Mutation42
MCM6minichromosome maintenance complex component 62Rare Single Gene Mutation42
MCPH1microcephalin 18Rare Single Gene Mutation415
MEGF10multiple EGF like domains 105Rare Single Gene Mutation, Genetic Association45
MEGF11multiple EGF like domains 1115Rare Single Gene Mutation44
MIB1Mindbomb E3 ubiquitin protein ligase 118Rare Single Gene Mutation45
MKL2MKL/myocardin-like 216Rare Single Gene Mutation, Genetic Association410
MNTMAX network transcriptional repressor17Genetic Association41
MPP6membrane palmitoylated protein 67Rare Single Gene Mutation43
MSANTD2Myb/SANT DNA binding domain containing 211Rare Single Gene Mutation41
MSR1macrophage scavenger receptor 18Rare Single Gene Mutation42
MUC12mucin 12, cell surface associated7Rare Single Gene Mutation42
MUC4mucin 4, cell surface associated3Rare Single Gene Mutation45
MYH4Myosin, heavy chain 4, skeletal muscle17Rare Single Gene Mutation43
MYO16myosin XVI13Rare Single Gene Mutation, Genetic Association47
MYO1Emyosin IE15Rare Single Gene Mutation42
MYO5Cmyosin VC15Rare Single Gene Mutation42
NAALADL2N-acetylated alpha-linked acidic dipeptidase-like 23Genetic Association41
NBEAneurobeachin13Rare Single Gene Mutation48
NCKAP5NCK-associated protein 52Rare Single Gene Mutation41
NCOR1nuclear receptor corepressor 117Rare Single Gene Mutation43
NDUFA5NADH dehydrogenase (ubiquinone) 1 alpha subcomplex, 5, 13kDa7Genetic Association43
NEO1Neogenin 11541
NLGN4Yneuroligin 4, Y-linkedYGenetic Association43
NPAS2neuronal PAS domain protein 22Genetic Association44
NR1D1nuclear receptor subfamily 1 group D member 117Rare Single Gene Mutation43
NRCAMneuronal cell adhesion molecule7Rare Single Gene Mutation, Genetic Association45
NRP2neuropilin 22Rare Single Gene Mutation, Genetic Association48
NTNG1netrin G11Rare Single Gene Mutation, Syndromic, Genetic Association4S8
NUP133nucleoporin 133kDa1Rare Single Gene Mutation44
NSMCE3NSE3 homolog, SMC5-SMC6 complex component15Functional43
ODF3L2outer dense fiber of sperm tails 3-like 219Rare Single Gene Mutation41
OFD1OFD1, centriole and centriolar satellite proteinXRare Single Gene Mutation42
OR1C1olfactory receptor, family 1, subfamily C, member 11Rare Single Gene Mutation42
OR2M4Olfactory receptor, family 2, subfamily M, member 41Genetic Association41
OR2T10olfactory receptor family 2 subfamily T member 101Rare Single Gene Mutation43
OTX1Orthodenticle homeobox 12Genetic Association43
PCDH10protocadherin 104Rare Single Gene Mutation48
PCDH11Xprotocadherin 11 X-linkedXRare Single Gene Mutation42
PCDH15Protocadherin-related 1510Rare Single Gene Mutation, Genetic Association44
PCDHA1Protocadherin alpha 15Rare Single Gene Mutation, Genetic Association43
PCDHA10Protocadherin alpha 105Rare Single Gene Mutation, Genetic Association43
PCDHA11Protocadherin alpha 115Rare Single Gene Mutation, Genetic Association44
PCDHA12Protocadherin alpha 125Rare Single Gene Mutation, Genetic Association43
PCDHA13Protocadherin alpha 135Rare Single Gene Mutation, Genetic Association44
PCDHA2Protocadherin alpha 25Rare Single Gene Mutation, Genetic Association44
PCDHA3Protocadherin alpha 35Rare Single Gene Mutation, Genetic Association43
PCDHA4Protocadherin alpha 45Rare Single Gene Mutation, Genetic Association44
PCDHA5Protocadherin alpha 55Rare Single Gene Mutation, Genetic Association45
PCDHA6Protocadherin alpha 65Rare Single Gene Mutation, Genetic Association43
PCDHA7Protocadherin alpha 75Rare Single Gene Mutation, Genetic Association43
PCDHA8Protocadherin alpha 85Rare Single Gene Mutation, Genetic Association44
PCDHA9Protocadherin alpha 95Rare Single Gene Mutation, Genetic Association44
PCDHAC1Protocadherin alpha subfamily C, 15Genetic Association42
PCDHAC2Protocadherin alpha subfamily C, 25Genetic Association43
PDCD1programmed cell death 12Rare Single Gene Mutation43
PATJPATJ, crumbs cell polarity complex component1Rare Single Gene Mutation42
PER1period homolog 1 (Drosophila)17Rare Single Gene Mutation, Genetic Association46
PITX1paired-like homeodomain 15Rare Single Gene Mutation, Genetic Association46
PLAURPlasminogen activator, urokinase receptor19Genetic Association41
PLNphospholamban6Rare Single Gene Mutation44
PLXNA3plexin A3XRare Single Gene Mutation42
POLA2DNA polymerase alpha 2, accessory subunit11Rare Single Gene Mutation42
POMT1protein O-mannosyltransferase 19Rare Single Gene Mutation42
POT1Protection of telomeres 1 homolog (S. pombe)7Rare Single Gene Mutation41
PPP1R1BProtein phosphatase 1, regulatory (inhibitor) subunit 1B17Genetic Association41
PPP2R1Bprotein phosphatase 2 regulatory subunit A, beta11Rare Single Gene Mutation44
QRICH1glutamine rich 13Rare Single Gene Mutation42
RIT2Ras-like without CAAX 218Genetic Association43
RPS6KA3Ribosomal protein S6 kinase, 90kDa, polypeptide 3XRare Single Gene Mutation, Syndromic4S9
SMG6Smg-6 homolog, nonsense mediated mRNA decay factor (C. elegans)17Rare Single Gene Mutation42
SNAP25Synaptosomal-associated protein, 25kDa20Rare Single Gene Mutation, Genetic Association46
TTNtitin2Rare Single Gene Mutation, Syndromic4S17
SATB2SATB homeobox 22Rare Single Gene Mutation, Syndromic, Genetic Association4S21
XPO1Exportin 1 (CRM1 homolog, yeast)2Rare Single Gene Mutation, Genetic Association45
SLC1A1solute carrier family 1 (neuronal/epithelial high affinity glutamate transporter, system Xag), member 19Rare Single Gene Mutation, Genetic Association411
SLC25A12solute carrier family 25 (mitochondrial carrier, Aralar), member 122Rare Single Gene Mutation, Genetic Association, Functional420
REREArginine-glutamic acid dipeptide (RE) repeats1Rare Single Gene Mutation, Syndromic, Genetic Association4S6
ZNF462Zinc finger protein 4629Rare Single Gene Mutation, Syndromic4S7
SLC4A10solute carrier family 4, sodium bicarbonate transporter-like, member 102Rare Single Gene Mutation, Genetic Association46
TANC2etratricopeptide repeat, ankyrin repeat and coiled-coil containing 217Rare Single Gene Mutation45
UNC80unc-80 homolog, NALCN activator2Rare Single Gene Mutation44
PSD3pleckstrin and Sec7 domain containing 38Rare Single Gene Mutation, Genetic Association45
PTPN11protein tyrosine phosphatase, non-receptor type 1112Rare Single Gene Mutation, Syndromic4S12
RPL10ribosomal protein L10XRare Single Gene Mutation, Syndromic413
SETDB2SET domain, bifurcated 213Rare Single Gene Mutation, Syndromic42
SLC6A4solute carrier family 6 (neurotransmitter transporter, serotonin), member 417Rare Single Gene Mutation, Genetic Association425
SLC6A8solute carrier family 6 (neurotransmitter transporter, creatine), member 8XRare Single Gene Mutation, Syndromic410
SLC9A9solute carrier family 9 (sodium/hydrogen exchanger), member 93Rare Single Gene Mutation, Genetic Association, Functional411
SYN1Synapsin 1XRare Single Gene Mutation, Functional417
SYN2Synapsin II3Rare Single Gene Mutation, Genetic Association, Functional46
TBX1T-box 122Syndromic41
TUBGCP5tubulin, gamma complex associated protein 515Rare Single Gene Mutation44
WNK3WNK lysine deficient protein kinase 3XRare Single Gene Mutation46
PRUNE2prune homolog 29Rare Single Gene Mutation, Syndromic46
RAB39BRAB39B, member RAS oncogene familyXRare Single Gene Mutation410
SIN3ASIN3 transcription regulator family member A15Rare Single Gene Mutation, Syndromic4S6
SYNE1spectrin repeat containing, nuclear envelope 16Rare Single Gene Mutation, Genetic Association4S15
TSPAN7tetraspanin 7XRare Single Gene Mutation47
PRPF39pre-mRNA processing factor 3914Rare Single Gene Mutation43
PTBP2polypyrimidine tract binding protein 21Rare Single Gene Mutation43
PTGS2prostaglandin-endoperoxide synthase 2 (prostaglandin G/H synthase and cyclooxyge nase)1Genetic Association45
PTPRBprotein tyrosine phosphatase, receptor type B12Rare Single Gene Mutation, Genetic Association43
RAB11FIP5RAB11 family interacting protein 52Rare Single Gene Mutation44
RAD21L1RAD21 cohesin complex component like 120Rare Single Gene Mutation42
RAPGEF4Rap guanine nucleotide exchange factor (GEF) 42Rare Single Gene Mutation415
REEP3receptor accessory protein 310Rare Single Gene Mutation43
RFX3regulatory factor X39Rare Single Gene Mutation45
RGS7regulator of G-protein signaling 71Rare Single Gene Mutation46
RHOXF1Rhox homeobox family, member 1XGenetic Association43
RIMS3regulating synaptic membrane exocytosis 31Rare Single Gene Mutation44
RNF135Ring finger protein 13517Syndromic, Genetic Association4S2
RNF38ring finger protein 389Rare Single Gene Mutation42
RPS6KA2ribosomal protein S6 kinase, 90kDa, polypeptide 26Rare Single Gene Mutation43
SCFD2sec1 family domain containing 24Rare Single Gene Mutation42
SCN4ASodium channel, voltage gated, type IV alpha subunit17Rare Single Gene Mutation43
SCP2sterol carrier protein 21Rare Single Gene Mutation42
SDC2syndecan 2 (heparan sulfate proteoglycan 1, cell surface-associated, fibroglycan )8Rare Single Gene Mutation, Genetic Association44
SETD1BSET domain containing 1B12Rare Single Gene Mutation, Syndromic4S6
SETDB1SET domain, bifurcated 11Rare Single Gene Mutation43
SEZ6L2SEZ6L2 seizure related 6 homolog (mouse)-like 216Rare Single Gene Mutation, Genetic Association46
SGSM3Small G protein signaling modulator 322Rare Single Gene Mutation44
SLC22A15Solute carrier family 22, member 151Genetic Association41
SLC22A9solute carrier family 22 member 911Rare Single Gene Mutation43
SLC25A27Solute carrier family 25, member 276Genetic Association41
RP11-1407O15.217Rare Single Gene Mutation41
SLC25A39solute carrier family 25 member 3917Rare Single Gene Mutation43
SLC27A4Solute carrier family 27 (fatty acid transporter), member 49Rare Single Gene Mutation41
SLC29A4solute carrier family 29 member 47Rare Single Gene Mutation41
SLC7A7solute carrier family 7 member 714Rare Single Gene Mutation42
SLCO1B3Solute carrier organic anion transporter family, member 1B312Rare Single Gene Mutation42
SMC3structural maintenance of chromosomes 310Rare Single Gene Mutation, Syndromic4S6
SND1staphylococcal nuclease and tudor domain containing 17Rare Single Gene Mutation, Genetic Association48
SNTG2Syntrophin, gamma 22Rare Single Gene Mutation45
SOD1superoxide dismutase 121Genetic Association, Functional42
SPP2secreted phosphoprotein 22Rare Single Gene Mutation43
SRGAP3SLIT-ROBO Rho GTPase activating protein 33Rare Single Gene Mutation43
SSPOSCO-spondin7Rare Single Gene Mutation43
SSRP1structure specific recognition protein 111Rare Single Gene Mutation42
ST7suppression of tumorigenicity 77Rare Single Gene Mutation44
STK39serine threonine kinase 39 (STE20/SPS1 homolog, yeast)2Genetic Association45
STX1ASyntaxin 1A (brain)7Rare Single Gene Mutation, Genetic Association46
STYK1Serine/threonine/tyrosine kinase 112Genetic Association41
SYAP1Synapse associated protein 1XRare Single Gene Mutation42
SYNJ1synaptojanin 121Rare Single Gene Mutation41
SYT17synaptotagmin XVII16Genetic Association42
TAF1CTATA-box binding protein associated factor, RNA polymerase I subunit C16Rare Single Gene Mutation, Genetic Association42
TBC1D5TBC1 domain family, member 53Rare Single Gene Mutation, Genetic Association47
TBL1Xtransducin (beta)-like 1X-linkedXGenetic Association41
TDO2tryptophan 2,3-dioxygenase4Genetic Association44
TECTAtectorin alpha11Rare Single Gene Mutation45
TERB2telomere repeat binding bouquet formation protein 215Rare Single Gene Mutation41
THBS1Thrombospondin 115Rare Single Gene Mutation, Genetic Association42
TM4SF19transmembrane 4 L six family member 193Rare Single Gene Mutation43
TOP3BTopoisomerase (DNA) III beta22Rare Single Gene Mutation, Genetic Association, Functional45
TPOThyroid peroxidase2Genetic Association41
TRIM33Tripartite motif containing 331Genetic Association41
TSHZ3teashirt zinc finger homeobox 319Rare Single Gene Mutation42
TSPAN17tetraspanin 175Rare Single Gene Mutation43
TTC25tetratricopeptide repeat domain 2517Genetic Association41
TSPOAP1TSPO associated protein 117Rare Single Gene Mutation45
UBE2Hubiquitin-conjugating enzyme E2H (UBC8 homolog, yeast)7Genetic Association42
UNC13Aunc-13 homolog A19Rare Single Gene Mutation, Syndromic4S5
USH2Ausherin1Rare Single Gene Mutation43
USP9Yubiquitin specific peptidase 9, Y-linkedYRare Single Gene Mutation, Genetic Association42
VASH1vasohibin 114Genetic Association44
VSIG4V-set and immunoglobulin domain containing 4XRare Single Gene Mutation42
WNT1Wingless-type MMTV integration site family, member 112Genetic Association43
YTHDC2YTH domain containing 25Rare Single Gene Mutation, Genetic Association45
YWHAETyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein, epsilon polypeptide17Rare Single Gene Mutation45
ZBTB16Zinc finger and BTB domain containing 1611Genetic Association41
ZNF18zinc finger protein 1817Rare Single Gene Mutation41
ZNF292zinc finger protein 2926Rare Single Gene Mutation43
ZNF385BZinc finger protein 385B2Genetic Association42
ZNF517Zinc finger protein 5178Rare Single Gene Mutation42
ZNF548zinc finger protein 54819Rare Single Gene Mutation42
ZNF559Zinc finger protein 55919Rare Single Gene Mutation43
ZNF626zinc finger protein 62619Rare Single Gene Mutation42
ZNF713Zinc finger protein 7137Rare Single Gene Mutation41
ZNF774Zinc finger protein 77415Rare Single Gene Mutation42
ZNF827Zinc finger protein 8274Genetic Association41
ZWILCHzwilchkinetochore protein15Rare Single Gene Mutation43

5 Category 5   [157 genes]

Status Gene Symbol Gene Name Chromosome Genetic Category Gene Score Syndromic reports
CAMSAP2calmodulin regulated spectrin-associated protein family, member 21Rare Single Gene Mutation51
CDKN1Bcyclin dependent kinase inhibitor 1B1251
CXCR3chemokine (C-X-C motif) receptor 3XRare Single Gene Mutation58
DIAPH3Diaphanous-related formin 313Rare Single Gene Mutation, Genetic Association511
DLG4discs large MAGUK scaffold protein 417Rare Single Gene Mutation, Syndromic, Functional59
GLRA2glycine receptor, alpha 2XRare Single Gene Mutation513
FGFBP3fibroblast growth factor binding protein 310Rare Single Gene Mutation51
CAMTA1calmodulin binding transcription activator 11Rare Single Gene Mutation57
CREBBPCREB binding protein16Rare Single Gene Mutation, Syndromic, Genetic Association519
FABP3Fatty acid binding protein 3, muscle and heart (mammary-derived growth inhibitor)1Functional51
FGD1FYVE, RhoGEF and PH domain containing 1XRare Single Gene Mutation, Syndromic53
DOCK10Dedicator of cytokinesis 102Rare Single Gene Mutation51
ARHGAP24Rho GTPase activating protein 244Rare Single Gene Mutation51
ESR1estrogen receptor 16Syndromic, Genetic Association59
GABRB1gamma-aminobutyric acid (GABA) A receptor, beta 14Rare Single Gene Mutation, Genetic Association56
FAM19A2family with sequence similarity 19 member A2, C-C motif chemokine like12Functional51
APCadenomatosis polyposis coli5Rare Single Gene Mutation, Genetic Association, Functional59
GANGigaxonin16Rare Single Gene Mutation51
ADARB1Adenosine deaminase, RNA-specific, B121Rare Single Gene Mutation, Functional52
ALOX5AParachidonate 5-lipoxygenase-activating protein3Functional54
AMBRA1autophagy and beclin 1 regulator 111Functional53
APPAmyloid beta (A4) precursor protein21Functional53
ARHGAP33Rho GTPase activating protein 3319Rare Single Gene Mutation, Functional52
ASS1argininosuccinate synthetase9Functional53
ATG7Autophagy related 73Functional52
ATP8A1ATPase phospholipid transporting 8A14Rare Single Gene Mutation, Functional52
ATRNL1Attractin-like 110Rare Single Gene Mutation51
ATXN7Ataxin 73Rare Single Gene Mutation51
AVPArginine vasopressin20Genetic Association, Functional54
BAIAP2BAI1-associated protein 217Rare Single Gene Mutation, Genetic Association510
BDNFBrain-derived neurotrophic factor11Rare Single Gene Mutation, Functional510
BRINP1BMP/retinoic acid inducible neural specific 19Functional52
CBLN1cerebellin 1 precursor16Genetic Association, Functional56
CD44CD44 molecule (Indian blood group)11Rare Single Gene Mutation, Functional54
CHD5chromodomain helicase DNA binding protein 51Rare Single Gene Mutation, Functional54
CLSTN2calsyntenin 23Rare Single Gene Mutation, Functional54
CLSTN3Calsyntenin 312Rare Single Gene Mutation, Functional52
CNR2Cannabinoid receptor 2 (macrophage)1Rare Single Gene Mutation, Genetic Association, Functional54
CRHR2corticotropin releasing hormone receptor 27Functional53
DAB1disabled homolog 1 (Drosophila)1Rare Single Gene Mutation, Functional57
DAPK1death-associated protein kinase 19Rare Single Gene Mutation, Genetic Association, Functional55
DCTN5dynactin 516Rare Single Gene Mutation53
DCUN1D1DCN1, defective in cullin neddylation 1, domain containing 1 (S. cerevisiae)3Functional53
DDX11DEAD/H (Asp-Glu-Ala-Asp/His) box polypeptide 1112Functional53
DGKKdiacylglycerol kinase kappaXFunctional51
DLX1distal-less homeobox 12Genetic Association58
DNAJC19DnaJ (Hsp40) homolog, subfamily C, member 193Functional51
DNM1LDynamin 1-like12Rare Single Gene Mutation, Functional53
DVL1Dishevelled segment polarity protein 11Functional53
EGR2early growth response 2 (Krox-20 homolog, Drosophila)10Functional54
EIF4EBP2Eukaryotic translation initiation factor 4E binding protein 210Functional51
EML1echinoderm microtubule associated protein like 114Rare Single Gene Mutation52
EPHA6EPH receptor A63Rare Single Gene Mutation56
EPHB6EPH receptor B67Rare Single Gene Mutation55
EPS8epidermal growth factor receptor pathway substrate 812Functional51
ERBB4v-erb-a erythroblastic leukemia viral oncogene homolog 4 (avian)2Rare Single Gene Mutation514
F13A1coagulation factor XIII, A1 polypeptide6Rare Single Gene Mutation, Functional56
FAM19A3family with sequence similarity 19 member A3, C-C motif chemokine like1Functional52
FLT1fms-related tyrosine kinase 1 (vascular endothelial growth factor/vascular perme ability factor receptor)13Rare Single Gene Mutation, Functional54
FOLH1Folate hydrolase (prostate-specific membrane antigen) 111Functional52
GABRA1Gamma-aminobutyric acid (GABA) A receptor, alpha 15Rare Single Gene Mutation, Functional56
GABRA5gamma-aminobutyric acid type A receptor alpha5 subunit15Genetic Association, Functional58
GABRQGamma-aminobutyric acid (GABA) A receptor, thetaXRare Single Gene Mutation51
GAD1Glutamate decarboxylase 1 (brain, 67kDa)2Rare Single Gene Mutation, Functional55
GADD45BGrowth arrest and DNA-damage-inducible, beta19Rare Single Gene Mutation, Functional54
GAP43Growth associated protein 433Functional51
PPP1R3Fprotein phosphatase 1, regulatory (inhibitor) subunit 3FXRare Single Gene Mutation53
KCNJ2Potassium inwardly-rectifying channel, subfamily J, member 217Rare Single Gene Mutation51
POU3F2POU class 3 homeobox 26Rare Single Gene Mutation, Functional53
GRPRGastrin-releasing peptide receptorXRare Single Gene Mutation, Genetic Association58
GPR139G protein-coupled receptor 13916Rare Single Gene Mutation55
GRIK4Glutamate receptor, ionotropic, kainate 411Rare Single Gene Mutation, Functional53
PDZD4PDZ domain containing 4XRare Single Gene Mutation54
GRM4Glutamate receptor, metabotropic 46Functional51
GSK3BGlycogen synthase kinase 3 beta3Rare Single Gene Mutation, Functional54
H2AFZH2A histone family member Z4Genetic Association, Functional53
HDAC3histone deacetylase 35Rare Single Gene Mutation, Functional55
HDChistidine decarboxylase15Rare Single Gene Mutation, Functional56
KCNT1Potassium channel, subfamily T, member 19Rare Single Gene Mutation, Syndromic510
HOXB1homeobox B117Rare Single Gene Mutation, Genetic Association58
HTR2A5-hydroxytryptamine (serotonin) receptor 2A13Rare Single Gene Mutation, Genetic Association59
IFNGinterferon gamma12Functional513
IFNGR1interferon gamma receptor 16Functional51
IL17AInterleukin 17A6Functional51
IL17RAinterleukin 17 receptor A22Rare Single Gene Mutation, Functional53
IL6interleukin 67Functional55
ITGA4integrin, alpha 4 (antigen CD49D, alpha 4 subunit of VLA-4 receptor)2Genetic Association55
ITGB7integrin, beta 712Rare Single Gene Mutation, Functional54
JAKMIP1Janus kinase and microtubule interacting protein 14Rare Single Gene Mutation, Functional58
KHDRBS3KH RNA binding domain containing, signal transduction associated 38Functional52
KLC2Kinesin light chain 211Rare Single Gene Mutation52
LAMC3laminin, gamma 39Rare Single Gene Mutation58
LATlinker for activation of T-cells16Functional52
MAGED1Melanoma antigen family D, 1XFunctional51
MALmal, T-cell differentiation protein2Functional52
MAP2microtubule-associated protein 22Rare Single Gene Mutation, Functional55
MAPK1Mitogen-activated protein kinase 122Rare Single Gene Mutation, Functional52
MAPK8IP2Mitogen-activated protein kinase 8 interacting protein 222Functional51
MOCOSMolybdenum cofactor sulfurase18Rare Single Gene Mutation, Functional52
MSNMoesinXFunctional51
MTR5-methyltetrahydrofolate-homocysteine methyltransferase1Rare Single Gene Mutation, Functional55
MTX2Metaxin 22Functional51
MYO1Amyosin IA12Rare Single Gene Mutation57
NCKAP5LNCK-associated protein 5-like12Rare Single Gene Mutation52
NEFLNeurofilament, light polypeptide8Rare Single Gene Mutation, Genetic Association52
NOS1APnitric oxide synthase 1 (neuronal) adaptor protein1Rare Single Gene Mutation56
NOS2nitric oxide synthase 217Rare Single Gene Mutation, Genetic Association57
NRG1Neuregulin 18Functional54
OPRM1opioid receptor, mu 16Functional54
P2RX4Purinergic receptor P2X, ligand-gated ion channel, 412Functional51
PAFAH1B1Platelet-activating factor acetylhydrolase 1b, regulatory subunit 1 (45kDa)17Functional52
PCDHGA11protocadherin gamma subfamily A, 115Rare Single Gene Mutation51
PDE4Bphosphodiesterase 4B, cAMP-specific1Rare Single Gene Mutation, Genetic Association, Functional55
PECRperoxisomal trans-2-enoyl-CoA reductase2Rare Single Gene Mutation52
PGLYRP2peptidoglycan recognition protein 219Rare Single Gene Mutation, Functional53
PINX1PIN2/TERF1 interacting, telomerase inhibitor 18Rare Single Gene Mutation55
PLCD1phospholipase C, delta 13Rare Single Gene Mutation59
PLPPR4phospholipid phosphatase related 41Functional53
PSMD10proteasome (prosome, macropain) 26S subunit, non-ATPase, 10XRare Single Gene Mutation56
PTGER3prostaglandin E receptor 31Rare Single Gene Mutation51
RAC1Rac family small GTPase 17Syndromic, Functional54
SLC16A7Solute carrier family 16, member 7 (monocarboxylic acid transporter 2)12Rare Single Gene Mutation51
RBM8ARNA binding motif protein 8A1Rare Single Gene Mutation, Functional55
RORARAR-related orphan receptor A15Rare Single Gene Mutation, Genetic Association, Functional517
TNIP2TNFAIP3 interacting protein 24Rare Single Gene Mutation51
UPF2UPF2 regulator of nonsense transcripts homolog (yeast)10Rare Single Gene Mutation54
SH3KBP1SH3-domain kinase binding protein 1XRare Single Gene Mutation54
TLK2tousled-like kinase 217Rare Single Gene Mutation59
UBE3Bubiquitin protein ligase E3B12Rare Single Gene Mutation, Syndromic55
PVALBParvalbumin22Functional52
RB1CC1RB1-inducible coiled-coil 18Rare Single Gene Mutation55
RBMS3RNA binding motif, single stranded interacting protein 33Rare Single Gene Mutation52
RFWD2ring finger and WD repeat domain 21Rare Single Gene Mutation, Genetic Association59
WNT2wingless-type MMTV integration site family member 27Rare Single Gene Mutation, Genetic Association510
ROBO1roundabout, axon guidance receptor, homolog 1 (Drosophila)3Rare Single Gene Mutation, Functional510
SLC25A14Solute carrier family 25 (mitochondrial carrier, brain), member 14XFunctional51
SLC25A24Solute carrier family 25 (mitochondrial carrier; phosphate carrier), member 241Rare Single Gene Mutation, Functional52
SLC30A3solute carrier family 30 member 32Functional52
SLC30A5solute carrier family 305Rare Single Gene Mutation53
SLC33A1solute carrier family 33 member 13Functional54
SNRPNsmall nuclear ribonucleoprotein polypeptide N15Rare Single Gene Mutation55
SRRM4Serine/arginine repetitive matrix 412Rare Single Gene Mutation, Functional55
STAT1signal transducer and activator of transcription 12Rare Single Gene Mutation, Functional52
SYN3Synapsin III22Rare Single Gene Mutation, Functional52
TERTtelomerase reverse transcriptase5Rare Single Gene Mutation, Functional52
TOMM20Translocase of outer mitochondrial membrane 20 homolog (yeast)1Functional51
TOP1Topoisomerase (DNA) I20Rare Single Gene Mutation, Functional56
TSNtranslin2Functional53
TYRtyrosinase11Rare Single Gene Mutation, Functional53
UBA6Ubiquitin-like modifier activating enzyme 64Functional52
UBR7ubiquitin protein ligase E3 component n-recognin 7 (putative)14Rare Single Gene Mutation51
UCN3urocortin 310Functional51
UPB1beta-ureidopropionase 122Rare Single Gene Mutation51
VLDLRVery low density lipoprotein receptor9Functional53
VRK3vaccinia related kinase 319Functional51
WDR93WD repeat domain 9315Rare Single Gene Mutation51
ZNF8Zinc finger protein 819Rare Single Gene Mutation51

6 Category 6   [21 genes]

Status Gene Symbol Gene Name Chromosome Genetic Category Gene Score Syndromic reports
DUSP22dual specificity phosphatase 226Rare Single Gene Mutation61
AFF4AF4/FMR2 family, member 45Rare Single Gene Mutation, Syndromic67
FABP7fatty acid binding protein 7, brain6Rare Single Gene Mutation, Genetic Association, Functional67
BTAF1RNA polymerase II, B-TFIID transcription factor-associated, 170kDa (Mot1 homolog, S. cerevisiae)10Rare Single Gene Mutation64
ARHGAP15Rho GTPase activating protein 152Rare Single Gene Mutation67
BCL2B-cell CLL/lymphoma 218Functional610
CHST5carbohydrate sulfotransferase 516Rare Single Gene Mutation65
CSNK1Dcasein kinase 1, delta17Rare Single Gene Mutation61
GNA14Guanine nucleotide binding protein (G protein), alpha 149Rare Single Gene Mutation61
MED12mediator complex subunit 12XRare Single Gene Mutation, Syndromic, Genetic Association620
GRM8glutamate receptor, metabotropic 87Rare Single Gene Mutation, Genetic Association67
HTR75-hydroxytryptamine (serotonin) receptor 7 (adenylate cyclase-coupled)10Rare Single Gene Mutation, Genetic Association65
PCDH8protocadherin 813Rare Single Gene Mutation61
UBL7ubiquitin-like 7 (bone marrow stromal cell-derived)15Rare Single Gene Mutation61
TPH2tryptophan hydroxylase 212Rare Single Gene Mutation, Genetic Association612
SLC16A3solute carrier family 16, member 3 (monocarboxylic acid transporter 4)17Rare Single Gene Mutation62
SUCLG2succinate-CoA ligase, GDP-forming, beta subunit3Rare Single Gene Mutation64
TAF1LTAF1 RNA polymerase II9Rare Single Gene Mutation63
TGM3transglutaminase 320Rare Single Gene Mutation65
XIRP1xin actin-binding repeat containing 13Rare Single Gene Mutation67
ZSWIM5zinc finger, SWIM-type containing 51Rare Single Gene Mutation61
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