Search results: The pahtway p3641 has 22 genes in the original annotation. Currently, there are 15 genes in SZGR 2.0 (with evidence in schizophrenia) that are present at this pathway.

Because the gene page contains a lot of information, it takes on average 3-5 seconds to load. So when you click a gene ID, please be patient for the page to load.

Gene ID Symbol Synonyms Official Full Name Location SZ group ? Functional group ?
5017OVOL1HOVO1ovo like zinc finger 111q13CV:PGCnp
DMG:Wockner_2014
5241PGRNR3C3 | PRprogesterone receptor11q22-q23CV:PGCnp
DMG:Jaffe_2016
PMID:cooccur
6927HNF1AHNF-1A | HNF1 | IDDM20 | LFB1 | MODY3 | TCF-1 | TCF1HNF1 homeobox A12q24.2CV:PGCnp
DMG:Wockner_2014
Network
3975LHX1LIM-1 | LIM1LIM homeobox 117q12CNV:YES
CV:PGCnp
GO_Annotation
PMID:cooccur
1435CSF1CSF-1 | MCSFcolony stimulating factor 11p13.3CV:PGCnp
DMG:Wockner_2014
GSMA_I
23566LPAR3EDG7 | Edg-7 | GPCR | HOFNH30 | LP-A3 | LPA3 | RP4-678I3lysophosphatidic acid receptor 31p22.3CV:GWASdb
CV:PGCnp
DNM:Fromer_2014
Expression
GO_Annotation
CompositeSet
5743PTGS2COX-2 | COX2 | GRIPGHS | PGG/HS | PGHS-2 | PHS-2 | hCox-2prostaglandin-endoperoxide synthase 21q25.2-q25.3Association
CV:GWAScat
CV:GWASdb
CV:PGCnp
PMID:cooccur
875CBSHIP4cystathionine-beta-synthase21q22.3CV:PGCnp
PMID:cooccur
7476WNT7A-wingless-type MMTV integration site family member 7A3p25CV:GWASdb
CV:PGCnp
DMG:Jaffe_2016
GO_Annotation
GSMA_I
3977LIFRCD118 | LIF-R | SJS2 | STWS | SWSleukemia inhibitory factor receptor alpha5p13-p12PMID:cooccur
7015TERTCMM9 | DKCA2 | DKCB4 | EST2 | PFBMFT1 | TCS1 | TP2 | TRT | hEST2 | hTRTtelomerase reverse transcriptase5p15.33CV:PGCnp
DMG:Wockner_2014
PMID:cooccur
Chromatin Remodeling Genes
3206HOXA10HOX1 | HOX1.8 | HOX1H | PLhomeobox A107p15.2DMG:Jaffe_2016
3207HOXA11HOX1 | HOX1I | RUSAT1homeobox A117p15.2CV:PGCnp
DMG:Jaffe_2016
DMG:Wockner_2014
4693NDPEVR2 | FEVR | NDNorrie disease (pseudoglioma)Xp11.4CV:PGCnp
GO_Annotation
PMID:cooccur
2182ACSL4ACS4 | FACL4 | LACS4 | MRX63 | MRX68acyl-CoA synthetase long-chain family member 4Xq22.3-q23CV:PGCnp
DNM:Fromer_2014
CompositeSet
Potential synaptic genes