Mental Impairment Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
External Link https://www.disgenet.org/browser/0/1/0/C0683322
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Genes

62 genes associated with the disease Mental Impairment in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
ADNP activity-dependent neuroprotector homeobox
AGPAT2 1-acylglycerol-3-phosphate O-acyltransferase 2
APOE apolipoprotein E
ARG1 arginase 1
ARID1B AT rich interactive domain 1B (SWI1-like)
ARSD arylsulfatase D
ASXL3 additional sex combs like transcriptional regulator 3
ATRX alpha thalassemia/mental retardation syndrome X-linked
BDNF brain-derived neurotrophic factor
BSCL2 Berardinelli-Seip congenital lipodystrophy 2 (seipin)
CACNA1A calcium channel, voltage-dependent, P/Q type, alpha 1A subunit
CACNA1G calcium channel, voltage-dependent, T type, alpha 1G subunit
CHL1 cell adhesion molecule L1-like
CNTNAP2 contactin associated protein-like 2
CPEB1 cytoplasmic polyadenylation element binding protein 1
CYP3A4 cytochrome P450, family 3, subfamily A, polypeptide 4
DLG3 discs, large homolog 3 (Drosophila)
DLG4 discs, large homolog 4 (Drosophila)
DMD dystrophin
DYRK1A dual-specificity tyrosine-(Y)-phosphorylation regulated kinase 1A
EP300 E1A binding protein p300
FA2H fatty acid 2-hydroxylase
FAM19A2 family with sequence similarity 19 (chemokine (C-C motif)-like), member A2
FMR1 fragile X mental retardation 1
FOXC2 forkhead box C2
FOXG1 forkhead box G1
GABARAP GABA(A) receptor-associated protein
GBA2 glucosidase, beta (bile acid) 2
GCG glucagon
GPNMB glycoprotein (transmembrane) nmb
GPS2 G protein pathway suppressor 2
GRIN2B glutamate receptor, ionotropic, N-methyl D-aspartate 2B
HDAC4 histone deacetylase 4
HERC1 HECT and RLD domain containing E3 ubiquitin protein ligase family member 1
HRAS Harvey rat sarcoma viral oncogene homolog
KCNH4 potassium channel, voltage gated eag related subfamily H, member 4
KIAA2022 KIAA2022
KLHL15 kelch-like family member 15
KMT2A lysine (K)-specific methyltransferase 2A
KMT2E lysine (K)-specific methyltransferase 2E
LAMA2 laminin, alpha 2
MAOA monoamine oxidase A
MAOB monoamine oxidase B
MEF2C myocyte enhancer factor 2C
NOS3 nitric oxide synthase 3 (endothelial cell)
NSD1 nuclear receptor binding SET domain protein 1
NSD2 nuclear receptor binding SET domain protein 2
NUFIP2 nuclear fragile X mental retardation protein interacting protein 2
PAH phenylalanine hydroxylase
PITX3 paired-like homeodomain 3
RELN reelin
SCN2A sodium channel, voltage gated, type II alpha subunit
SLC2A1 solute carrier family 2 (facilitated glucose transporter), member 1
SLC9A6 solute carrier family 9, subfamily A (NHE6, cation proton antiporter 6), member 6
SPG11 spastic paraplegia 11 (autosomal recessive)
STAT5B signal transducer and activator of transcription 5B
TCF12 transcription factor 12
TUBB tubulin, beta class I
TUBB4A tubulin, beta 4A class IVa
UBA5 ubiquitin-like modifier activating enzyme 5
VCX variable charge, X-linked
VPS13B vacuolar protein sorting 13 homolog B (yeast)