Search results: The pahtway p3323 has 88 genes in the original annotation. Currently, there are 47 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 ?
1586CYP17A1CPT7 | CYP17 | P450C17 | S17AHcytochrome P450 family 17 subfamily A member 110q24.3CV:GWAScat
CV:PGC128
CV:PGCnp
GO_Annotation
LK:YES
83401ELOVL3CIG-30 | CIG30ELOVL fatty acid elongase 310q24.32CV:PGCnp
196743PAOXPAOpolyamine oxidase (exo-N4-amino)10q26.3CV:PGCnp
DMG:Jaffe_2016
GSMA_IIA
2620GAS2-growth arrest specific 211p14.3CV:PGCnp
PMID:cooccur
5805PTSPTPS6-pyruvoyltetrahydropterin synthase11q22.3GO_Annotation
GSMA_I
PMID:cooccur
219854TMEM218-transmembrane protein 21811q24.2CV:PGCnp
DMG:Wockner_2014
4257MGST1GST12 | MGST | MGST-Imicrosomal glutathione S-transferase 112p12.3-p12.1CV:PGCnp
26353HSPB8CMT2L | DHMN2 | E2IG1 | H11 | HMN2 | HMN2A | HSP22heat shock protein family B (small) member 812q24.23CV:PGCnp
5983RFC3RFC38replication factor C subunit 313q13.2CV:PGCnp
DMG:Jaffe_2016
1152CKBB-CK | BCK | CKBB | HEL-211 | HEL-S-29creatine kinase, brain14q32CV:PGCnp
PMID:cooccur		INTRACELLULAR SIGNAL TRANSDUCTION
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_Synaptosome
G2Cdb.humanPSD
G2Cdb.humanPSP
CompositeSet
Darnell FMRP targets
55505NOP10DKCB1 | NOLA3 | NOP10PNOP10 ribonucleoprotein15q14-q15CV:PGCnp
56963RGMARGMrepulsive guidance molecule family member a15q26.1CV:PGCnp
PMID:cooccur
5579PRKCBPKC-beta | PKCB | PRKCB1 | PRKCB2protein kinase C beta16p11.2CV:PGCnp
DMG:Jaffe_2016
DNM:Xu_2012
Network		CANABINOID
INTRACELLULAR SIGNAL TRANSDUCTION
METABOTROPIC GLUTAMATE RECEPTOR
SEROTONIN
G2Cdb.human_BAYES-COLLINS-HUMAN-PSD-FULL
G2Cdb.humanNRC
CompositeSet
Darnell FMRP targets
Potential synaptic genes
11051NUDT21CFIM25 | CPSF5nudix hydrolase 2116q12.2CV:PGCnp
DMG:Nishioka_2013
Network
4502MT2AMT2metallothionein 2A16q13CV:PGCnp
PMID:cooccur
84268RPAINHRIP | RIPRPA interacting protein17p13.2CV:PGCnp
DMG:Jaffe_2016
8689KRT36HA6 | KRTHA6 | hHa6keratin 3617q21.2CV:GWASdb
CV:PGCnp
27106ARRDC2CLONE24945 | PP2703arrestin domain containing 219p13.11CV:PGCnp
DMG:vanEijk_2014
374291NDUFS7CI-20 | CI-20KD | MY017 | PSSTNADH:ubiquinone oxidoreductase core subunit S719p13.3CV:PGCnp
PMID:cooccur
1628DBPDABPD site of albumin promoter (albumin D-box) binding protein19q13.3CV:PGCnp
DEG:Sanders_2013
PMID:cooccur
3283HSD3B13BETAHSD | HSD3B | HSDB3 | HSDB3A | I | SDR11E1hydroxy-delta-5-steroid dehydrogenase, 3 beta- and steroid delta-isomerase 11p13.1CV:GWASdb
CV:PGCnp
GSMA_I
GSMA_IIA
PMID:cooccur
2134EXTL1EXTLexostosin-like glycosyltransferase 11p36.1CV:PGCnp
DNM:Fromer_2014		CompositeSet
3925STMN1C1orf215 | LAP18 | Lag | OP18 | PP17 | PP19 | PR22 | SMNstathmin 11p36.11CV:PGCnp
GO_Annotation
PMID:cooccur		STRUCTURAL PLASTICITY
2987GUK1GMKguanylate kinase 11q32-q41CV:PGCnp
DMG:Wockner_2014
140885SIRPABIT | CD172A | MFR | MYD-1 | P84 | PTPNS1 | SHPS1 | SIRPsignal regulatory protein alpha20p13CV:PGCnp
DMG:Wockner_2014		TYROSINE KINASE SIGNALING
G2Cdb.human_BAYES-COLLINS-HUMAN-PSD-CONSENSUS
CompositeSet
150379PNPLA5GS2L | dJ388M5 | dJ388M5.4patatin like phospholipase domain containing 522q13.31CV:PGCnp
4190MDH1HEL-S-32 | MDH-s | MDHA | MGC:1375 | MOR2malate dehydrogenase 12p13.3CV:PGCnp
DMG:Jaffe_2016
DMG:Wockner_2014
PMID:cooccur		CELL METABOLISM
CompositeSet
130271PLEKHH2PLEKHH1Lpleckstrin homology, MyTH4 and FERM domain containing H22p21CV:PGCnp
DNM:McCarthy_2014
55289ACOXL-acyl-CoA oxidase-like2q13CV:GWASdb
CV:PGCnp
GSMA_I
GSMA_IIA
4292MLH1COCA2 | FCC2 | HNPCC | HNPCC2 | hMLH1mutL homolog 13p21.3CV:PGCnp
GSMA_I
7869SEMA3BLUCA-1 | SEMA5 | SEMAA | SemA | semaVsemaphorin 3B3p21.3DMG:Wockner_2014
GO_Annotation
5745PTH1RPFE | PTHR | PTHR1parathyroid hormone 1 receptor3p22-p21.1CV:PGCnp
DMG:Wockner_2014
Network
6565SLC15A2PEPT2solute carrier family 15 member 23q13.33CV:PGCnp
Expression
7468WHSC1MMSET | NSD2 | REIIBP | TRX5 | WHSWolf-Hirschhorn syndrome candidate 14p16.3CV:PGCnp
DMG:Wockner_2014		Chromatin Remodeling Genes
22915MMRN1ECM | EMILIN4 | GPIa* | MMRNmultimerin 14q22CV:PGCnp
126ADH1CADH3alcohol dehydrogenase 1C (class I), gamma polypeptide4q23CV:PGCnp
PMID:cooccur
79071ELOVL6FACE | FAE | LCEELOVL fatty acid elongase 64q25CV:GWASdb
CV:PGCnp
DEG:Sanders_2013
DMG:Jaffe_2016
DMG:Wockner_2014
3796KIF2ACDCBM3 | HK2 | KIF2kinesin heavy chain member 2A5q12-q13Association
CV:GWASdb
CV:PGCnp
DMG:Jaffe_2016
GO_Annotation
PMID:cooccur		STRUCTURAL PLASTICITY
G2Cdb.human_BAYES-COLLINS-HUMAN-PSD-CONSENSUS
G2Cdb.human_BAYES-COLLINS-HUMAN-PSD-FULL
G2Cdb.human_BAYES-COLLINS-MOUSE-PSD-CONSENSUS
CompositeSet
Potential synaptic genes
3008HIST1H1EH1.4 | H1E | H1F4 | H1s-4 | dJ221C16.5histone cluster 1, H1e6p21.3CV:GWASdb
CV:PGCnp
DNM:Xu_2012
GSMA_I
PMID:cooccur		G2Cdb.humanPSD
G2Cdb.humanPSP
CompositeSet
3018HIST1H2BBH2B.1 | H2B/f | H2BFFhistone cluster 1, H2bb6p21.3CV:PGCnp
GSMA_I
85236HIST1H2BKH2B/S | H2BFAiii | H2BFT | H2BKhistone cluster 1, H2bk6p21.33CV:PGCnp
GSMA_I
8345HIST1H2BHH2B/j | H2BFJhistone cluster 1, H2bh6p22.2CV:PGCnp
DEG:Sanders_2013
GSMA_I
PMID:cooccur
670BPHLBPH-RP | MCNAA | VACVASEbiphenyl hydrolase-like (serine hydrolase)6p25CV:PGCnp
GSMA_I
10799RPP40RNASEP1 | bA428J1.3ribonuclease P/MRP 40kDa subunit6p25.1CV:PGCnp
GSMA_I
254228FAM26EC6orf188 | dJ493F7.3family with sequence similarity 26 member E6q22.1CV:GWASdb
CV:PGCnp
79020C7orf25-chromosome 7 open reading frame 257p14.1CV:PGCnp
4128MAOAMAO-Amonoamine oxidase AXp11.3Association
CV:PGCnp
GO_Annotation
GR_Ng
PMID:cooccur		DOPAMINE
NEUROTRANSMITTER METABOLISM
SEROTONIN
G2Cdb.human_BAYES-COLLINS-HUMAN-PSD-CONSENSUS
G2Cdb.human_BAYES-COLLINS-HUMAN-PSD-FULL
G2Cdb.human_clathrin
G2Cdb.human_Synaptosome
G2Cdb.humanPSD
G2Cdb.humanPSP
CompositeSet
Potential synaptic genes