attention deficit hyperactivity disorder Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description A specific developmental disorder that is characterized by co-existence of attentional problems and hyperactivity, with each behavior occurring infrequently alone and symptoms starting before seven years of age. (Human Disease Ontology, DOID_1094)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0007018
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Genes

88 genes associated with the attention deficit hyperactivity disorder phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
ABCD1 ATP-binding cassette, sub-family D (ALD), member 1
ARVCF armadillo repeat gene deleted in velocardiofacial syndrome
ASPM asp (abnormal spindle) homolog, microcephaly associated (Drosophila)
BAZ1B bromodomain adjacent to zinc finger domain, 1B
BCR breakpoint cluster region
CHD7 chromodomain helicase DNA binding protein 7
CHRNA7 cholinergic receptor, nicotinic, alpha 7 (neuronal)
CLIP2 CAP-GLY domain containing linker protein 2
COMT catechol-O-methyltransferase
COX1
COX2
COX3
CRKL v-crk avian sarcoma virus CT10 oncogene homolog-like
DHCR7 7-dehydrocholesterol reductase
DYM dymeclin
ELN elastin
FGD1 FYVE, RhoGEF and PH domain containing 1
FLII flightless I homolog (Drosophila)
FMR1 fragile X mental retardation 1
GATA4 GATA binding protein 4
GNAQ guanine nucleotide binding protein (G protein), q polypeptide
GNE glucosamine (UDP-N-acetyl)-2-epimerase/N-acetylmannosamine kinase
GP1BB glycoprotein Ib (platelet), beta polypeptide
GRIN2A glutamate receptor, ionotropic, N-methyl D-aspartate 2A
GTF2I general transcription factor IIi
GTF2IRD1 GTF2I repeat domain containing 1
HDAC4 histone deacetylase 4
HDAC8 histone deacetylase 8
HIRA histone cell cycle regulator
HSPG2 heparan sulfate proteoglycan 2
IKBKG inhibitor of kappa light polypeptide gene enhancer in B-cells, kinase gamma
LHCGR luteinizing hormone/choriogonadotropin receptor
LIG4 ligase IV, DNA, ATP-dependent
LIMK1 LIM domain kinase 1
MAPK1 mitogen-activated protein kinase 1
MED12 mediator complex subunit 12
MLH1 mutL homolog 1
MSH2 mutS homolog 2
MSH6 mutS homolog 6
MT-ND4 NADH dehydrogenase, subunit 4 (complex I)
MT-ND5 NADH dehydrogenase, subunit 5 (complex I)
MT-ND6 NADH dehydrogenase, subunit 6 (complex I)
MT-TF tRNA
MT-TH tRNA
MT-TL1 tRNA
MT-TQ tRNA
MT-TS1 tRNA
MT-TS2 tRNA
MT-TW tRNA
NBN nibrin
ND1
NDN necdin, melanoma antigen (MAGE) family member
NDP Norrie disease (pseudoglioma)
NIPBL Nipped-B homolog (Drosophila)
NSUN2 NOP2/Sun RNA methyltransferase family, member 2
OCRL oculocerebrorenal syndrome of Lowe
OPHN1 oligophrenin 1
PAH phenylalanine hydroxylase
PCNT pericentrin
PIEZO2 piezo-type mechanosensitive ion channel component 2
PMS2 PMS2 postmeiotic segregation increased 2 (S. cerevisiae)
PRKCG protein kinase C, gamma
PTCH1 patched 1
RAD21 RAD21 homolog (S. pombe)
RAI1 retinoic acid induced 1
RFC2 replication factor C (activator 1) 2, 40kDa
SATB2 SATB homeobox 2
SEMA3E sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3E
SH2B1 SH2B adaptor protein 1
SIM1 single-minded family bHLH transcription factor 1
SLC6A8 solute carrier family 6 (neurotransmitter transporter), member 8
SLITRK1 SLIT and NTRK-like family, member 1
SMC1A structural maintenance of chromosomes 1A
SMC3 structural maintenance of chromosomes 3
SNRPN small nuclear ribonucleoprotein polypeptide N
SPRED1 sprouty-related, EVH1 domain containing 1
SRCAP Snf2-related CREBBP activator protein
STS steroid sulfatase (microsomal), isozyme S
TBL2 transducin (beta)-like 2
TBX1 T-box 1
THRB thyroid hormone receptor, beta
TMCO1 transmembrane and coiled-coil domains 1
TSC1 tuberous sclerosis 1
TSC2 tuberous sclerosis 2
UFD1L ubiquitin fusion degradation 1 like (yeast)
UPF3B UPF3 regulator of nonsense transcripts homolog B (yeast)
VPS13A vacuolar protein sorting 13 homolog A (S. cerevisiae)
ZDHHC9 zinc finger, DHHC-type containing 9