Search results: The pahtway p2622 has 74 genes in the original annotation. Currently, there are 48 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 ?
3988LIPACESD | LALlipase A, lysosomal acid type10q23.2-q23.3CV:GWASdb
CV:PGCnp
3434IFIT1C56 | G10P1 | IFI-56 | IFI-56K | IFI56 | IFIT-1 | IFNAI1 | ISG56 | P56 | RNM561interferon induced protein with tetratricopeptide repeats 110q23.31CV:PGCnp
PMID:cooccur
355FASALPS1A | APO-1 | APT1 | CD95 | FAS1 | FASTM | TNFRSF6Fas cell surface death receptor10q24.1CV:PGCnp
Expression
GR_Ng
GR_WM
Network
PMID:cooccur
8519IFITM19-27 | CD225 | DSPA2a | IFI17 | LEU13interferon induced transmembrane protein 111p15.5DMG:Montano_2016
Expression
PMID:cooccur
694BTG1-B-cell translocation gene 1, anti-proliferative12q22CV:PGCnp
DMG:Jaffe_2016
PMID:cooccur
4939OAS2-2'-5'-oligoadenylate synthetase 212q24.2CV:GWASdb
CV:PGCnp
8638OASLOASLd | TRIP-14 | TRIP14 | p59 OASL | p59-OASL | p59OASL2'-5'-oligoadenylate synthetase like12q24.2CV:PGCnp
5720PSME1HEL-S-129m | IFI5111 | PA28A | PA28alpha | REGalphaproteasome activator subunit 114q11.2GSMA_I
PMID:cooccur
567B2MIMD43beta-2-microglobulin15q21.1CV:PGCnp
PMID:cooccur
5371PMLMYL | PP8675 | RNF71 | TRIM19promyelocytic leukemia15q22CV:PGCnp
DNM:Xu_2012
Network
PMID:cooccur
CompositeSet
5699PSMB10LMP10 | MECL1 | beta2iproteasome subunit beta 1016q22.1CV:PGCnp
Expression
3430IFI35IFP35interferon induced protein 3517q21CV:PGCnp
4089SMAD4DPC4 | JIP | MADH4 | MYHRSSMAD family member 418q21.1CV:PGCnp
DMG:Jaffe_2016
DMG:Nishioka_2013
Network
PMID:cooccur
5366PMAIP1APR | NOXAphorbol-12-myristate-13-acetate-induced protein 118q21.32CV:PGCnp
DMG:Jaffe_2016
4294MAP3K10MEKK10 | MLK2 | MSTmitogen-activated protein kinase kinase kinase 1019q13.2CV:PGCnp
DMG:Jaffe_2016
389RHOCARH9 | ARHC | H9 | RHOH9ras homolog family member C1p13.1CV:PGCnp
DMG:Jaffe_2016
GSMA_I
2633GBP1-guanylate binding protein 11p22.2CV:PGCnp
PMID:cooccur
10561IFI44MTAP44 | TLDC5 | p44interferon induced protein 441p31.1CV:PGCnp
GSMA_IIA
533ATP6V0BATP6F | HATPL | VMA16ATPase H+ transporting V0 subunit b1p32.3CV:PGCnp
103ADARADAR1 | AGS6 | DRADA | DSH | DSRAD | G1P1 | IFI-4 | IFI4 | K88DSRBP | P136adenosine deaminase, RNA-specific1q21.3CV:PGCnp
DMG:Jaffe_2016
GSMA_I
GSMA_IIA
PMID:cooccur
G2Cdb.humanPSD
G2Cdb.humanPSP
Ascano FMRP targets
6726SRP9ALURBPsignal recognition particle 9kDa1q42.12CV:PGCnp
DMG:Nishioka_2013
4599MX1IFI-78K | IFI78 | MX | MxAMX dynamin like GTPase 121q22.3CV:PGCnp
PMID:cooccur
4600MX2MXBMX dynamin like GTPase 221q22.3CV:PGCnp
DMG:Wockner_2014
PMID:cooccur
10521DDX17P72 | RH70DEAD-box helicase 1722q13.1CV:PGCnp
DMG:Nishioka_2013
678ZFP36L2BRF2 | ERF-2 | ERF2 | RNF162C | TIS11DZFP36 ring finger protein-like 22p22.3-p21CV:PGCnp
DMG:Montano_2016
9111NMI-N-myc and STAT interactor2q23CV:PGCnp
GSMA_IIA
PMID:cooccur
6772STAT1CANDF7 | IMD31A | IMD31B | IMD31C | ISGF-3 | STAT91signal transducer and activator of transcription 12q32.2CV:PGCnp
Network
PMID:cooccur
G2Cdb.human_BAYES-COLLINS-HUMAN-PSD-FULL
G2Cdb.humanPSD
G2Cdb.humanPSP
841CASP8ALPS2B | CAP4 | Casp-8 | FLICE | MACH | MCH5caspase 82q33-q34CV:GWASdb
CV:PGCnp
3431SP110IFI41 | IFI75 | IPR1 | VODISP110 nuclear body protein2q37.1CV:GWASdb
CV:PGCnp
DMG:Wockner_2014
Expression
5530PPP3CACALN | CALNA | CALNA1 | CCN1 | CNA1 | PPP2Bprotein phosphatase 3 catalytic subunit alpha4q24CV:PGCnp
GO_Annotation
Network
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_TAP-PSD-95-CORE
G2Cdb.humanNRC
G2Cdb.humanPSD
G2Cdb.humanPSP
CompositeSet
Darnell FMRP targets
Potential synaptic genes
3660IRF2IRF-2interferon regulatory factor 24q35.1CV:PGCnp
DMG:Jaffe_2016
6500SKP1EMC19 | OCP-II | OCP2 | SKP1A | TCEB1L | p19AS-phase kinase-associated protein 15q31DMG:Wockner_2014
Expression
PMID:cooccur
INTRACELLULAR SIGNAL TRANSDUCTION
3659IRF1IRF-1 | MARinterferon regulatory factor 15q31.1CV:PGCnp
DMG:Jaffe_2016
GSMA_I
3107HLA-CD6S204 | HLA-JY3 | HLAC | HLC-C | PSORS1major histocompatibility complex, class I, C6p21.3CV:GWASdb
CV:PGCnp
DNM:Xu_2012
GSMA_I
Network
PMID:cooccur
CompositeSet
3133HLA-EEA1.2 | EA2.1 | HLA-6.2 | MHC | QA1major histocompatibility complex, class I, E6p21.3CV:GWASdb
CV:PGCnp
DMG:Jaffe_2016
GSMA_I
7726TRIM26AFP | RNF95 | ZNF173tripartite motif containing 266p21.3CV:GWAScat
CV:GWASdb
CV:PGCnp
GSMA_I
PMID:cooccur
6890TAP1ABC17 | ABCB2 | APT1 | D6S114E | PSF-1 | PSF1 | RING4 | TAP1*0102N | TAP1Ntransporter 1, ATP-binding cassette, sub-family B (MDR/TAP)6p21.3CV:GWASdb
CV:PGCnp
DMG:Jaffe_2016
DMG:Wockner_2014
GSMA_I
PMID:cooccur
5696PSMB8ALDD | D6S216 | D6S216E | JMP | LMP7 | NKJO | PSMB5i | RING10proteasome subunit beta 86p21.3CV:GWASdb
CV:PGCnp
DMG:Jaffe_2016
DMG:Montano_2016
GSMA_I
5698PSMB9LMP2 | PSMB6i | RING12 | beta1iproteasome subunit beta 96p21.3CV:PGCnp
DMG:Jaffe_2016
DMG:Nishioka_2013
DMG:Wockner_2014
GSMA_I
3105HLA-AAw-33 | Aw-74 | HLAAmajor histocompatibility complex, class I, A6p21.3CV:GWAScat
CV:GWASdb
CV:PGCnp
GSMA_I
PMID:cooccur
2766GMPRGMPR 1 | GMPR1guanosine monophosphate reductase6p23CV:GWASdb
CV:PGCnp
DMG:Jaffe_2016
GSMA_I
PMID:cooccur
8763CD164DFNA66 | MGC-24 | MUC-24 | endolynCD164 molecule6q21CV:PGCnp
DMG:Jaffe_2016
3569IL6BSF-2 | BSF2 | CDF | HGF | HSF | IFN-beta-2 | IFNB2 | IL-6interleukin 67p21CV:GWASdb
CV:PGCnp
PMID:cooccur
7979SHFM1DSS1 | ECD | SEM1 | SHFD1 | SHSF1 | Shfdg1split hand/foot malformation (ectrodactyly) type 17q21.3CV:PGCnp
PMID:cooccur
6742SSBP1Mt-SSB | SOSS-B1 | SSBP | mtSSBsingle-stranded DNA binding protein 1, mitochondrial7q34DMG:Nishioka_2013
6386SDCBPMDA-9 | MDA9 | ST1 | SYCL | TACIP18syndecan binding protein8q12CV:PGCnp
DMG:Nishioka_2013
GO_Annotation
Network
Potential synaptic genes
573BAG1BAG-1 | HAP | RAP46BCL2 associated athanogene 19p12CV:PGCnp
Expression
PMID:cooccur
9830TRIM14-tripartite motif containing 149q22.33CV:PGCnp
DMG:Wockner_2014