Search results: The pahtway p4180 has 35 genes in the original annotation. Currently, there are 24 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 ?
7417VDAC2PORvoltage dependent anion channel 210q22DMG:Wockner_2014
PMID:cooccur		G2Cdb.human_BAYES-COLLINS-HUMAN-PSD-CONSENSUS
G2Cdb.human_BAYES-COLLINS-HUMAN-PSD-FULL
G2Cdb.human_BAYES-COLLINS-MOUSE-PSD-CONSENSUS
G2Cdb.human_clathrin
G2Cdb.human_mitochondria
G2Cdb.human_Synaptosome
G2Cdb.human_TAP-PSD-95-CORE
G2Cdb.humanNRC
G2Cdb.humanPSD
G2Cdb.humanPSP
CompositeSet
79053ALG8CDG1HALG8, alpha-1,3-glucosyltransferase11q14.1CV:PGCnp
7386UQCRFS1RIP1 | RIS1 | RISP | UQCR5ubiquinol-cytochrome c reductase, Rieske iron-sulfur polypeptide 119q12CV:GWASdb
CV:PGCnp
55851PSENENMDS033 | MSTP064 | PEN-2 | PEN2presenilin enhancer gamma secretase subunit19q13.12DMG:Jaffe_2016
DMG:Wockner_2014		NEUROTROPHIN SIGNALING
7812CSDE1D1S155E | UNRcold shock domain containing E11p22CV:PGCnp
GSMA_I
GSMA_IIA
4599MX1IFI-78K | IFI78 | MX | MxAMX dynamin like GTPase 121q22.3CV:PGCnp
PMID:cooccur
388RHOBARH6 | ARHB | MST081 | MSTP081 | RHOH6ras homolog family member B2p24CV:GWASdb
CV:PGCnp
DMG:Nishioka_2013
PMID:cooccur		INTRACELLULAR SIGNAL TRANSDUCTION
CompositeSet
Darnell FMRP targets
151011SEPT10-septin 102q13CV:GWASdb
CV:PGCnp
GSMA_I
GSMA_IIA		G2Cdb.human_BAYES-COLLINS-HUMAN-PSD-CONSENSUS
CompositeSet
8801SUCLG2GBETAsuccinate-CoA ligase, GDP-forming, beta subunit3p14.1CV:PGCnp
961CD47IAP | MER6 | OA3CD47 molecule3q13.1-q13.2CV:PGCnp
Expression
GSMA_IIA
GSMA_IIE
PMID:cooccur		CELL ADHESION AND TRANSSYNAPTIC SIGNALING
51714SELT-selenoprotein T3q25.1CV:PGCnp
DMG:Wockner_2014
6731SRP72BMFF | BMFS1 | HEL103signal recognition particle 72kDa4q11CV:PGCnp
DMG:Jaffe_2016
1635DCTD-dCMP deaminase4q35.1CV:GWASdb
CV:PGCnp
6880TAF9MGC:5067 | STAF31/32 | TAF2G | TAFII-31 | TAFII-32 | TAFII31 | TAFII32 | TAFIID32TATA-box binding protein associated factor 95q13.2DNM:Fromer_2014CompositeSet
6414SEPP1SELP | SEPP | SePselenoprotein P, plasma, 15q31CV:PGCnp
GO_Annotation
PMID:cooccur
7416VDAC1PORIN | VDAC-1voltage dependent anion channel 15q31CV:PGCnp
DMG:Jaffe_2016
DNM:Fromer_2014
GSMA_I
Network
PMID:cooccur		EXCITABILITY
G2Cdb.human_BAYES-COLLINS-HUMAN-PSD-CONSENSUS
G2Cdb.human_BAYES-COLLINS-HUMAN-PSD-FULL
G2Cdb.human_BAYES-COLLINS-MOUSE-PSD-CONSENSUS
G2Cdb.human_clathrin
G2Cdb.human_mitochondria
G2Cdb.human_Synaptosome
G2Cdb.human_TAP-PSD-95-CORE
G2Cdb.humanNRC
G2Cdb.humanPSD
G2Cdb.humanPSP
CompositeSet
Potential synaptic genes
2107ETF1D5S1995 | ERF | ERF1 | RF1 | SUP45L1 | TB3-1eukaryotic translation termination factor 15q31.1CV:GWAScat
CV:PGC128
CV:PGCnp
Expression
GSMA_I
Network
821CANXCNX | IP90 | P90calnexin5q35CV:PGCnp
DNM:Xu_2012
GSMA_IIA		RNA AND PROTEIN SYNTHESIS
CompositeSet
8992ATP6V0E1ATP6H | ATP6V0E | M9.2 | Vma21 | Vma21pATPase H+ transporting V0 subunit e15q35.1CV:PGCnp
GSMA_IIA
7803PTP4A1HH72 | PRL-1 | PRL1 | PTP(CAAX1) | PTPCAAX1protein tyrosine phosphatase type IVA, member 16q12CV:GWASdb
CV:PGCnp
10652YKT6-YKT6 v-SNARE homolog (S. cerevisiae)7p15.1CV:PGCnp
GO_Annotation
114049WBSCR22HASJ4442 | HUSSY-3 | MERM1 | PP3381 | WBMTWilliams Beuren syndrome chromosome region 227q11.23CNV:YES
CV:GWASdb
DMG:Nishioka_2013
6009RHEBRHEB2Ras homolog enriched in brain7q36CV:PGCnp
DMG:Wockner_2014
7534YWHAZ14-3-3-zeta | HEL-S-3 | HEL-S-93 | HEL4 | KCIP-1 | YWHADtyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein zeta8q23.1Association
CV:PGCnp
DMG:Wockner_2014
DNM:Fromer_2014
Network
PMID:cooccur		INTRACELLULAR SIGNAL TRANSDUCTION
G2Cdb.human_mGluR5
G2Cdb.human_mitochondria
G2Cdb.humanNRC
G2Cdb.humanPSD
G2Cdb.humanPSP
CompositeSet
Potential synaptic genes