obsessive-compulsive behavior Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0000722
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Genes

36 genes associated with the obsessive-compulsive behavior phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
ADNP activity-dependent neuroprotector homeobox
AFF2 AF4/FMR2 family, member 2
ALMS1 Alstrom syndrome protein 1
BAZ1B bromodomain adjacent to zinc finger domain, 1B
BCR breakpoint cluster region
CHD7 chromodomain helicase DNA binding protein 7
CLIP2 CAP-GLY domain containing linker protein 2
COASY CoA synthase
CRKL v-crk avian sarcoma virus CT10 oncogene homolog-like
DMPK dystrophia myotonica-protein kinase
DRD2 dopamine receptor D2
EHMT1 euchromatic histone-lysine N-methyltransferase 1
ELN elastin
FMR1 fragile X mental retardation 1
GTF2I general transcription factor IIi
GTF2IRD1 GTF2I repeat domain containing 1
HDAC4 histone deacetylase 4
HDAC8 histone deacetylase 8
LIMK1 LIM domain kinase 1
MAPK1 mitogen-activated protein kinase 1
MED12 mediator complex subunit 12
NIPBL Nipped-B homolog (Drosophila)
OCRL oculocerebrorenal syndrome of Lowe
PAH phenylalanine hydroxylase
PANK2 pantothenate kinase 2
RAD21 RAD21 homolog (S. pombe)
RFC2 replication factor C (activator 1) 2, 40kDa
SEMA3E sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3E
SETD5 SET domain containing 5
SGCE sarcoglycan, epsilon
SLITRK1 SLIT and NTRK-like family, member 1
SMC1A structural maintenance of chromosomes 1A
SMC3 structural maintenance of chromosomes 3
TBL2 transducin (beta)-like 2
TBX1 T-box 1
TTC19 tetratricopeptide repeat domain 19