short attention span Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Reduced attention span characterized by distractibility and impulsivity but not necessarily satisfying the diagnostic criteria for attention deficit hyperactivity disorder. (Human Phenotype Ontology, HP_0000736)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0000736
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Genes

97 genes associated with the short attention span phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
AASS aminoadipate-semialdehyde synthase
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)
AUH AU RNA binding protein/enoyl-CoA hydratase
BAZ1B bromodomain adjacent to zinc finger domain, 1B
BCR breakpoint cluster region
CC2D1A coiled-coil and C2 domain containing 1A
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
CREBBP CREB binding protein
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
IGF1 insulin-like growth factor 1 (somatomedin C)
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
MBD5 methyl-CpG binding domain protein 5
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
PAK3 p21 protein (Cdc42/Rac)-activated kinase 3
PCNT pericentrin
PIEZO2 piezo-type mechanosensitive ion channel component 2
PLA2G6 phospholipase A2, group VI (cytosolic, calcium-independent)
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
SOBP sine oculis binding protein homolog (Drosophila)
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