Proton-coupled amino acid transporter 1

Protein-coding gene in the species Homo sapiens From Wikipedia, the free encyclopedia

Proton-coupled amino acid transporter 1 is a protein that in humans is encoded by the SLC36A1 gene.[5][6][7]

AliasesSLC36A1, Dct1, LYAAT1, PAT1, TRAMD3, solute carrier family 36 member 1
End151,492,379 bp[1]
Quick facts SLC36A1, Identifiers ...
SLC36A1
Identifiers
AliasesSLC36A1, Dct1, LYAAT1, PAT1, TRAMD3, solute carrier family 36 member 1
External IDsOMIM: 606561; MGI: 2445299; HomoloGene: 121860; GeneCards: SLC36A1; OMA:SLC36A1 - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_001308150
NM_001308151
NM_078483
NM_001349740

NM_153139

RefSeq (protein)

NP_001295079
NP_001295080
NP_510968
NP_001336669

NP_694779

Location (UCSC)Chr 5: 151.44 – 151.49 MbChr 11: 55.1 – 55.13 Mb
PubMed search[3][4]
Wikidata
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This gene encodes a member of the eukaryote-specific amino acid/auxin permease (AAAP) 1 transporter family. The encoded protein functions as a proton-dependent, small amino acid transporter. This gene is clustered with related family members on chromosome 5q33.1.[7]

See also

References

Further reading

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