Search results: The pahtway p22 has 29 genes in the original annotation. Currently, there are 19 genes in SZGR 2.0 (with evidence in schizophrenia) that are present at this pathway.

Because the gene page contains a lot of information, it takes on average 3-5 seconds to load. So when you click a gene ID, please be patient for the page to load.

Gene ID Symbol Synonyms Official Full Name Location SZ group ? Functional group ?
221ALDH3B1ALDH4 | ALDH7aldehyde dehydrogenase 3 family member B111q13CV:PGCnp
DMG:vanEijk_2014
DMG:Wockner_2014
PMID:cooccur
3034HALHIS | HSTDhistidine ammonia-lyase12q23.1DMG:vanEijk_2014
PMID:cooccur
217ALDH2ALDH-E2 | ALDHI | ALDMaldehyde dehydrogenase 2 family (mitochondrial)12q24.2CV:PGCnp
DMG:Nishioka_2013
GO_Annotation
PMID:cooccur
CompositeSet
9836LCMT2PPM2 | TYW4leucine carboxyl methyltransferase 215q15.3CV:PGCnp
DMG:Jaffe_2016
3067HDC-histidine decarboxylase15q21.2CV:PGCnp
PMID:cooccur
220ALDH1A3ALDH1A6 | ALDH6 | MCOP8 | RALDH3aldehyde dehydrogenase 1 family member A315q26.3CV:PGCnp
DMG:Wockner_2014
PMID:cooccur
51451LCMT1CGI-68 | LCMT | PPMT1leucine carboxyl methyltransferase 116p12.1CV:PGCnp
DMG:Jaffe_2016
DMG:Wockner_2014
GSMA_IIE
224ALDH3A2ALDH10 | FALDH | SLSaldehyde dehydrogenase 3 family member A217p11.2CV:PGCnp
DMG:Wockner_2014
GO_Annotation
443ASPAACY2 | ASPaspartoacylase17p13.3CV:PGCnp
PMID:cooccur
84735CNDP1CN1 | CPGL2 | HsT2308carnosine dipeptidase 1 (metallopeptidase M20 family)18q22.3CV:PGCnp
DMG:Jaffe_2016
223ALDH9A1ALDH4 | ALDH7 | ALDH9 | E3 | TMABADHaldehyde dehydrogenase 9 family member A11q23.1CV:PGCnp
DMG:Nishioka_2013
GO_Annotation
PMID:cooccur
10841FTCDLCHC1formimidoyltransferase cyclodeaminase21q22.3CV:PGCnp
GO_Annotation
PMID:cooccur
3176HNMTHMT | HNMT-S1 | HNMT-S2 | MRT51histamine N-methyltransferase2q22.1CV:PGCnp
DEG:Sanders_2013
GSMA_I
GSMA_IIA
PMID:cooccur
501ALDH7A1ATQ1 | EPD | PDEaldehyde dehydrogenase 7 family member A15q31CV:PGCnp
DMG:Jaffe_2016
GSMA_I
CompositeSet
1644DDCAADCdopa decarboxylase7p12.2CV:PGCnp
PMID:cooccur
DOPAMINE
SEROTONIN
114049WBSCR22HASJ4442 | HUSSY-3 | MERM1 | PP3381 | WBMTWilliams Beuren syndrome chromosome region 227q11.23CNV:YES
CV:GWASdb
DMG:Nishioka_2013
219ALDH1B1ALDH5 | ALDHXaldehyde dehydrogenase 1 family member B19p11.1CV:GWASdb
CV:PGCnp
DMG:Jaffe_2016
4129MAOB-monoamine oxidase BXp11.23CV:PGCnp
GO_Annotation
PMID:cooccur
DOPAMINE
NEUROTRANSMITTER METABOLISM
SEROTONIN
CompositeSet
Potential synaptic genes
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