MGP Database

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MGP003614

Ontology/Pathway Information

Entrez Gene ID8604
Gene Namesolute carrier family 25 (aspartate/glutamate carrier), member 12
Gene Symbol SLC25A12
SpeciesHomo sapiens
Gene Ontology (GO Annotations)
GO IDSourceTypeDescription
GO:0016021 NAS:UniProtKBCintegral component of membrane
GO:0005743 TAS:ReactomeCmitochondrial inner membrane
GO:0005739 IDA:UniProtKBCmitochondrion
GO:0005509 IDA:UniProtKBFcalcium ion binding
GO:0015183 IDA:UniProtKBFL-aspartate transmembrane transporter activity
GO:0005313 IDA:UniProtKBFL-glutamate transmembrane transporter activity
GO:0015810 IDA:UniProtKBPaspartate transport
GO:0005975 TAS:ReactomePcarbohydrate metabolic process
GO:0006094 TAS:ReactomePgluconeogenesis
GO:0006006 TAS:ReactomePglucose metabolic process
GO:0089712 IDA:GOCPL-aspartate transmembrane transport
GO:0089711 IDA:GOCPL-glutamate transmembrane transport
GO:0015813 IDA:UniProtKBPL-glutamate transport
GO:0043490 IDA:UniProtKBPmalate-aspartate shuttle
GO:0051592 IDA:UniProtKBPresponse to calcium ion
GO:0044281 TAS:ReactomePsmall molecule metabolic process
REACTOME Pathway Links
REACTOME Pathway IDDescription
REACT_116125Disease
REACT_1520Gluconeogenesis
REACT_723Glucose metabolism
REACT_264090Glycogen storage diseases
REACT_111217Metabolism
REACT_474Metabolism of carbohydrates
REACT_17015Metabolism of proteins
REACT_118595Mitochondrial protein import
REACT_264430Myoclonic epilepsy of Lafora
SMP Pathway Links
SMP IDDescription
SMP00357Argininemia
SMP00003Argininosuccinic Aciduria
SMP00002Carbamoyl Phosphate Synthetase Deficiency
SMP00001Citrullinemia Type I
SMP00129Malate-Aspartate Shuttle
SMP00205Ornithine Transcarbamylase Deficiency (OTC Deficiency)
SMP00059Urea Cycle
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