Search results: The pahtway p2067 has 26 genes in the original annotation. Currently, there are 15 genes in SZGR 2.0 (with evidence in schizophrenia) that are present at this pathway.

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Gene ID Symbol Synonyms Official Full Name Location SZ group ? Functional group ?
5209PFKFB3IPFK2 | PFK2 | iPFK-26-phosphofructo-2-kinase/fructose-2,6-biphosphatase 310p15.1CV:PGCnp
DMG:Jaffe_2016
Ascano FMRP targets
960CD44CDW44 | CSPG8 | ECMR-III | HCELL | HUTCH-I | IN | LHR | MC56 | MDU2 | MDU3 | MIC4 | Pgp1CD44 molecule (Indian blood group)11p13CV:GWASdb
DMG:Jaffe_2016
DMG:Wockner_2014
Expression
Network
7262PHLDA2BRW1C | BWR1C | HLDA2 | IPL | TSSC3pleckstrin homology like domain family A member 211p15.4CV:PGCnp
DMG:Wockner_2014
10938EHD1H-PAST | HPAST1 | PAST | PAST1EH domain containing 111q13CV:PGCnp
DMG:Jaffe_2016
DMG:Nishioka_2013
DMG:Wockner_2014
CompositeSet
64750SMURF2-SMAD specific E3 ubiquitin protein ligase 217q22-q23CV:PGCnp
DMG:Jaffe_2016
51129ANGPTL4ARP4 | FIAF | HARP | HFARP | NL2 | PGAR | TGQTL | UNQ171 | pp1158angiopoietin like 419p13.3CV:PGCnp
GO_Annotation
PMID:cooccur
5329PLAURCD87 | U-PAR | UPAR | URKRplasminogen activator, urokinase receptor19q13CV:PGCnp
PMID:cooccur
51599LSRILDR3 | LISCH7lipolysis stimulated lipoprotein receptor19q13.12CV:GWASdb
CV:PGCnp
PMID:cooccur
2067ERCC1COFS4 | RAD10 | UV20excision repair cross-complementation group 119q13.32DMG:Jaffe_2016
4047LSSCTRCT44 | OSClanosterol synthase (2,3-oxidosqualene-lanosterol cyclase)21q22.3CV:PGCnp
DMG:Nishioka_2013
PMID:cooccur
6525SMTN-smoothelin22q12.2CV:PGCnp
GSMA_I
3241HPCAL1BDR1 | HLP2 | VILIP-3hippocalcin like 12p25.1CV:PGCnp
DMG:Nishioka_2013
DMG:Wockner_2014
INTRACELLULAR SIGNAL TRANSDUCTION
8853ASAP2AMAP2 | CENTB3 | DDEF2 | PAG3 | PAP | Pap-alpha | SHAG1ArfGAP with SH3 domain, ankyrin repeat and PH domain 22p25|2p24CV:PGCnp
DMG:Jaffe_2016
DNM:Gulsuner_2013
1839HBEGFDTR | DTS | DTSF | HEGFLheparin binding EGF like growth factor5q23CV:PGCnp
GSMA_I
6303SAT1DC21 | KFSD | KFSDX | SAT | SSAT | SSAT-1spermidine/spermine N1-acetyltransferase 1Xp22.1CV:PGCnp
PMID:cooccur
Potential synaptic genes