Search results: The pahtway p1922 has 58 genes in the original annotation. Currently, there are 33 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 ?
2237FEN1FEN-1 | MF1 | RAD2flap structure-specific endonuclease 111q12DMG:Nishioka_2013
DMG:Wockner_2014
PMID:cooccur
1111CHEK1CHK1checkpoint kinase 111q24.2CV:GWASdb
CV:PGCnp
Network
PMID:cooccur
5965RECQLRECQL1 | RecQ1RecQ like helicase12p12DMG:Jaffe_2016
5893RAD52-RAD52 homolog, DNA repair protein12p13-p12.2CV:PGCnp
7334UBE2NHEL-S-71 | UBC13 | UBCHBEN; UBC13 | UbcH-ben | UbcH13ubiquitin conjugating enzyme E2 N12q22CV:PGCnp
DMG:Jaffe_2016
DMG:vanEijk_2014
Expression
PMID:cooccur
RNA AND PROTEIN SYNTHESIS
G2Cdb.human_BAYES-COLLINS-HUMAN-PSD-CONSENSUS
CompositeSet
6996TDGhTDGthymine DNA glycosylase12q24.1CV:PGCnp
PMID:cooccur
5426POLECRCS12 | FILS | POLE1polymerase (DNA) epsilon, catalytic subunit12q24.3CV:PGCnp
PMID:cooccur
Ascano FMRP targets
328APEX1APE | APE1 | APEN | APEX | APX | HAP1 | REF1apurinic/apyrimidinic endodeoxyribonuclease 114q11.2DMG:Nishioka_2013
GSMA_I
Network
55775TDP1-tyrosyl-DNA phosphodiesterase 114q32.11CV:PGCnp
DMG:Nishioka_2013
2072ERCC4ERCC11 | FANCQ | RAD1 | XFEPS | XPFexcision repair cross-complementation group 416p13.12CV:PGCnp
GSMA_IIE
7157TP53BCC7 | LFS1 | P53 | TRP53tumor protein p5317p13.1Association
Core
CV:PGCnp
GO_Annotation
GR_COR
GR_Ng
GR_WM
Network
PMID:cooccur
672BRCA1BRCAI | BRCC1 | BROVCA1 | FANCS | IRIS | PNCA4 | PPP1R53 | PSCP | RNF53breast cancer 117q21CV:PGCnp
DMG:Wockner_2014
Network
PMID:cooccur
11201POLIRAD30B | RAD3OBpolymerase (DNA) iota18q21.1CV:PGCnp
PMID:cooccur
5886RAD23AHHR23A | HR23ARAD23 homolog A, nucleotide excision repair protein19p13.2CV:PGCnp
5424POLD1CDC2 | CRCS10 | MDPL | POLDpolymerase (DNA) delta 1, catalytic subunit19q13.3CV:PGCnp
DMG:Wockner_2014
Expression
2067ERCC1COFS4 | RAD10 | UV20excision repair cross-complementation group 119q13.32DMG:Jaffe_2016
9156EXO1HEX1 | hExoIexonuclease 11q43CV:GWASdb
CV:PGCnp
11200CHEK2CDS1 | CHK2 | HuCds1 | LFS2 | PP1425 | RAD53 | hCds1checkpoint kinase 222q12.1CV:PGCnp
DMG:Jaffe_2016
DNM:Gulsuner_2013
GSMA_I
2956MSH6GTBP | GTMBP | HNPCC5 | HSAP | p160mutS homolog 62p16CV:PGCnp
DMG:Nishioka_2013
Network
55120FANCLFAAP43 | PHF9 | POGFanconi anemia complementation group L2p16.1CV:PGCnp
5378PMS1HNPCC3 | MLH2 | PMSL1 | hPMS1PMS1 homolog 1, mismatch repair system component2q31.1CV:PGCnp
DMG:Jaffe_2016
DMG:Wockner_2014
113510HELQHEL308helicase, POLQ-like4q21.23CV:PGCnp
CV:PheWAS
1161ERCC8CKN1 | CSA | UVSS2excision repair cross-complementation group 85q12.1CV:PGCnp
51426POLKDINB1 | DINP | POLQpolymerase (DNA) kappa5q13CV:PGCnp
4439MSH5G7 | MUTSH5 | NG23mutS homolog 56p21.3CV:GWASdb
CV:PGCnp
GO_Annotation
GSMA_I
PMID:cooccur
2968GTF2H4P52 | TFB2 | TFIIHgeneral transcription factor IIH subunit 46p21.3CV:PGCnp
DMG:Jaffe_2016
GSMA_I
5980REV3LPOLZ | REV3REV3 like, DNA directed polymerase zeta catalytic subunit6q21CV:PGCnp
DMG:Jaffe_2016
CompositeSet
Darnell FMRP targets
7979SHFM1DSS1 | ECD | SEM1 | SHFD1 | SHSF1 | Shfdg1split hand/foot malformation (ectrodactyly) type 17q21.3CV:PGCnp
PMID:cooccur
252969NEIL2NEH2 | NEI2nei like DNA glycosylase 28p23.1CV:PGCnp
DMG:Jaffe_2016
5591PRKDCDNA-PKcs | DNAPK | DNPK1 | HYRC | HYRC1 | IMD26 | XRCC7 | p350protein kinase, DNA-activated, catalytic polypeptide8q11CV:PGCnp
DMG:vanEijk_2014
DNM:McCarthy_2014
GO_Annotation
Network
G2Cdb.human_BAYES-COLLINS-HUMAN-PSD-CONSENSUS
2189FANCGFAG | XRCC9Fanconi anemia complementation group G9p13CV:PGCnp
DMG:Jaffe_2016
54840APTXAOA | AOA1 | AXA1 | EAOH | EOAHA | FHA-HITaprataxin9p13.3CV:PGCnp
5887RAD23BHHR23B | HR23B | P58RAD23 homolog B, nucleotide excision repair protein9q31.2CV:PGCnp
DMG:Jaffe_2016