MGP Database

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MGP002849

Ontology/Pathway Information

Entrez Gene ID6510
Gene Namesolute carrier family 1 (neutral amino acid transporter), member 5
Gene Symbol SLC1A5
SpeciesHomo sapiens
Gene Ontology (GO Annotations)
GO IDSourceTypeDescription
GO:0070062 IDA:UniProtKBCextracellular vesicular exosome
GO:0005794 IDA:HPACGolgi apparatus
GO:0005887 TAS:ProtIncCintegral component of plasma membrane
GO:0042470 IEA:UniProtKB-SubCellCmelanosome
GO:0016020 IDA:UniProtKBCmembrane
GO:0005886 IDA:UniProtKBCplasma membrane
GO:0015186 TAS:BHF-UCLFL-glutamine transmembrane transporter activity
GO:0015194 IEA:EnsemblFL-serine transmembrane transporter activity
GO:0015175 TAS:ProtIncFneutral amino acid transmembrane transporter activity
GO:0004872 TAS:ProtIncFreceptor activity
GO:0017153 IEA:InterProFsodium:dicarboxylate symporter activity
GO:0001618 IEA:UniProtKB-KWFvirus receptor activity
GO:0006865 TAS:ReactomePamino acid transport
GO:0006860 IEA:EnsemblPextracellular amino acid transport
GO:0006868 TAS:BHF-UCLPglutamine transport
GO:0006811 TAS:ReactomePion transport
GO:0015804 TAS:ProtIncPneutral amino acid transport
GO:0055085 TAS:ReactomePtransmembrane transport
REACTOME Pathway Links
REACTOME Pathway IDDescription
REACT_13796Amino acid transport across the plasma membrane
REACT_19118SLC-mediated transmembrane transport
REACT_15518Transmembrane transport of small molecules
REACT_19397Transport of inorganic cations/anions and amino acids/oligopeptides
SMP Pathway Links
SMP IDDescription
SMP00357Argininemia
SMP00003Argininosuccinic Aciduria
SMP00002Carbamoyl Phosphate Synthetase Deficiency
SMP00001Citrullinemia Type I
SMP00205Ornithine Transcarbamylase Deficiency (OTC Deficiency)
SMP00059Urea Cycle
SMP00654Warburg Effect
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