MGP Database

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MGP006334

Ontology/Pathway Information

Entrez Gene ID113235
Gene Namesolute carrier family 46 (folate transporter), member 1
Gene Symbol SLC46A1
SpeciesHomo sapiens
Gene Ontology (GO Annotations)
GO IDSourceTypeDescription
GO:0016324 IDA:UniProtKBCapical plasma membrane
GO:0031526 IEA:EnsemblCbrush border membrane
GO:0009986 IDA:UniProtKBCcell surface
GO:0005737 ISS:UniProtKBCcytoplasm
GO:0016021 IEA:UniProtKB-KWCintegral component of membrane
GO:0005886 TAS:ReactomeCplasma membrane
GO:0005542 IEA:UniProtKB-KWFfolic acid binding
GO:0008517 IDA:UniProtKBFfolic acid transporter activity
GO:0015232 IEA:EnsemblFheme transporter activity
GO:0015350 IEA:EnsemblFmethotrexate transporter activity
GO:0006879 TAS:ReactomePcellular iron ion homeostasis
GO:0046655 TAS:ReactomePfolic acid metabolic process
GO:0015884 IDA:UniProtKBPfolic acid transport
GO:0044281 TAS:ReactomePsmall molecule metabolic process
GO:0055085 TAS:ReactomePtransmembrane transport
GO:0006766 TAS:ReactomePvitamin metabolic process
GO:0006767 TAS:ReactomePwater-soluble vitamin metabolic process
REACTOME Pathway Links
REACTOME Pathway IDDescription
REACT_169280Defective AMN causes hereditary megaloblastic anemia 1
REACT_169403Defective BTD causes biotidinase deficiency
REACT_169178Defective CD320 causes methylmalonic aciduria
REACT_169132Defective CUBN causes hereditary megaloblastic anemia 1
REACT_169415Defective GIF causes intrinsic factor deficiency
REACT_169312Defective HLCS causes multiple carboxylase deficiency
REACT_169363Defective LMBRD1 causes methylmalonic aciduria and homocystinuria type cblF
REACT_169316Defective MMAA causes methylmalonic aciduria type cblA
REACT_169318Defective MMAB causes methylmalonic aciduria type cblB
REACT_169169Defective MMACHC causes methylmalonic aciduria and homocystinuria type cblC
REACT_169256Defective MMADHC causes methylmalonic aciduria and homocystinuria type cblD
REACT_169149Defective MTR causes methylmalonic aciduria and homocystinuria type cblG
REACT_169439Defective MTRR causes methylmalonic aciduria and homocystinuria type cblE
REACT_169313Defective MUT causes methylmalonic aciduria mut type
REACT_169120Defective TCN2 causes hereditary megaloblastic anemia
REACT_169238Defects in biotin (Btn) metabolism
REACT_169429Defects in cobalamin (B12) metabolism
REACT_169385Defects in vitamin and cofactor metabolism
REACT_116125Disease
REACT_25060Iron uptake and transport
REACT_111217Metabolism
REACT_11167Metabolism of folate and pterines
REACT_11193Metabolism of vitamins and cofactors
REACT_11238Metabolism of water-soluble vitamins and cofactors
REACT_15518Transmembrane transport of small molecules
SMP Pathway Links
SMP IDDescription
SMP00724Folate malabsorption, hereditary
SMP00053Folate Metabolism
SMP00543Homocystinuria due to defect of N(5,10)-methylene THF deficiency
SMP00432Methotrexate Action Pathway
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