Search results: The pahtway p2192 has 38 genes in the original annotation. Currently, there are 31 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 ?
355FASALPS1A | APO-1 | APT1 | CD95 | FAS1 | FASTM | TNFRSF6Fas cell surface death receptor10q24.1CV:PGCnp
Expression
GR_Ng
GR_WM
Network
PMID:cooccur
1643DDB2DDBB | UV-DDB2 | XPEdamage specific DNA binding protein 211p11.2CV:PGCnp
8525DGKZDAGK5 | DAGK6 | DGK-ZETA | hDGKzetadiacylglycerol kinase zeta11p11.2CV:PGC128
CV:PGCnp
DMG:Wockner_2014
PMID:cooccur
G2Cdb.humanPSD
G2Cdb.humanPSP
CompositeSet
Darnell FMRP targets
4033LRMPJAW1lymphoid restricted membrane protein12p12.1CV:PGCnp
8079MLF2NTN4myeloid leukemia factor 212p13CV:PGCnp
DEG:Zhao_2015
DMG:vanEijk_2014
G2Cdb.human_BAYES-COLLINS-MOUSE-PSD-CONSENSUS
4193MDM2ACTFS | HDMX | hdm2MDM2 proto-oncogene12q14.3-q15CV:PGCnp
Network
PMID:cooccur
23479ISCU2310020H20Rik | HML | ISU2 | NIFU | NIFUN | hnifUiron-sulfur cluster assembly enzyme12q24.1CV:PGCnp
DMG:Jaffe_2016
1445CSK-c-src tyrosine kinase15q24.1CV:PGCnp
Network
PMID:cooccur
6521SLC4A1AE1 | BND3 | CD233 | CHC | DI | EMPB3 | EPB3 | FR | RTA1A | SAO | SPH4 | SW | WD | WD1 | WRsolute carrier family 4 member 1 (Diego blood group)17q21.31CV:PGCnp
Network
ION BALANCE
5414SEPT4ARTS | BRADEION | CE5B3 | H5 | MART | PNUTL2 | SEP4 | hCDCREL-2 | hucep-7septin 417q22CV:PGCnp
PMID:cooccur
G2Cdb.human_BAYES-COLLINS-HUMAN-PSD-CONSENSUS
G2Cdb.human_BAYES-COLLINS-HUMAN-PSD-FULL
G2Cdb.human_BAYES-COLLINS-MOUSE-PSD-CONSENSUS
G2Cdb.humanPSD
G2Cdb.humanPSP
CompositeSet
5329PLAURCD87 | U-PAR | UPAR | URKRplasminogen activator, urokinase receptor19q13CV:PGCnp
PMID:cooccur
6518SLC2A5GLUT-5 | GLUT5solute carrier family 2 member 51p36.2CV:PGCnp
DMG:Wockner_2014
6051RNPEPAP-Barginyl aminopeptidase1q32CV:PGCnp
DMG:Wockner_2014
5972RENHNFJ2renin1q32CV:PGCnp
GO_Annotation
PMID:cooccur
23046KIF21B-kinesin family member 21B1q32.1CV:GWAScat
CV:GWASdb
CV:PGCnp
DMG:Wockner_2014
CompositeSet
Darnell FMRP targets
9928KIF14MKS12kinesin family member 141q32.1CV:PGCnp
DNM:Fromer_2014
CompositeSet
421ARVCF-armadillo repeat gene deleted in velocardiofacial syndrome22q11.21Association
CNV:YES
CV:PGCnp
GR_WM
GSMA_I
PMID:cooccur
G2Cdb.humanPSD
G2Cdb.humanPSP
CompositeSet
Darnell FMRP targets
6948TCN2D22S676 | D22S750 | II | TC | TC II | TC-2 | TC2 | TCIItranscobalamin 222q12.2CV:PGCnp
GSMA_I
PMID:cooccur
150468CKAP2L-cytoskeleton associated protein 2 like2q13CV:GWAScat
CV:GWASdb
CV:PGCnp
DMG:Wockner_2014
GSMA_I
GSMA_IIA
55830GLT8D1AD-017 | MSTP139glycosyltransferase 8 domain containing 13p21.1CV:GWAScat
CV:GWASdb
CV:PGCnp
LK:YES
PMID:cooccur
7366UGT2B15HLUG4 | UDPGT 2B8 | UDPGT2B15 | UDPGTH3 | UGT2B8UDP glucuronosyltransferase family 2 member B154q13DMG:Wockner_2014
6622SNCANACP | PARK1 | PARK4 | PD1synuclein alpha4q21CV:PGCnp
DMG:Nishioka_2013
GO_Annotation
Network
PMID:cooccur
G2Cdb.human_clathrin
G2Cdb.human_Synaptosome
1839HBEGFDTR | DTS | DTSF | HEGFLheparin binding EGF like growth factor5q23CV:PGCnp
GSMA_I
26999CYFIP2PIR121cytoplasmic FMR1 interacting protein 25q33.3CV:GWASdb
CV:PGCnp
DMG:Wockner_2014
GO_Annotation
GSMA_I
GSMA_IIA
GSMA_IIE
PMID:cooccur
G2Cdb.human_BAYES-COLLINS-HUMAN-PSD-CONSENSUS
G2Cdb.human_BAYES-COLLINS-HUMAN-PSD-FULL
G2Cdb.human_BAYES-COLLINS-MOUSE-PSD-CONSENSUS
G2Cdb.humanPSD
G2Cdb.humanPSP
CompositeSet
Darnell FMRP targets
Ascano FMRP targets
5292PIM1PIMPim-1 proto-oncogene, serine/threonine kinase6p21.2CV:GWASdb
CV:PGCnp
DMG:Nishioka_2013
GSMA_I
GSMA_IIE
11074TRIM31C6orf13 | HCG1 | HCGI | RNFtripartite motif containing 316p21.3CV:GWASdb
CV:PGCnp
GSMA_I
7407VARSG7A | VARS1 | VARS2valyl-tRNA synthetase6p21.3CV:PGCnp
GSMA_I
Network
PMID:cooccur
Ascano FMRP targets
3486IGFBP3BP-53 | IBP3insulin like growth factor binding protein 37p12.3CV:PGCnp
PMID:cooccur
9883POM121P145 | POM121APOM121 transmembrane nucleoporin7q11.23CNV:YES
CV:PGCnp
DMG:Jaffe_2016
2824GPM6BM6Bglycoprotein M6BXp22.2CV:PGCnp
DEG:Zhao_2015
GO_Annotation
CELL ADHESION AND TRANSSYNAPTIC SIGNALING
Potential synaptic genes
546ATRXATR2 | JMS | MRX52 | MRXHF1 | RAD54 | RAD54L | SFM1 | SHS | XH2 | XNP | ZNF-HXalpha thalassemia/mental retardation syndrome X-linkedXq21.1CV:PGCnp
PMID:cooccur
G2Cdb.humanPSD
G2Cdb.humanPSP
Chromatin Remodeling Genes