SLC36A2

SLC36A2
Identifiers
Aliases	SLC36A2, PAT2, TRAMD1, solute carrier family 36 member 2
External IDs	MGI: 1891430 HomoloGene: 72100 GeneCards: SLC36A2
Gene location (Human) Chr. Chromosome 5 (human) Band No data available Start 151,314,978 bp End 151,347,590 bp
Gene location (Mouse) Chr. Chromosome 11 (mouse) Band No data available Start 55,158,470 bp End 55,185,077 bp
Gene ontology Molecular function • L-alanine transmembrane transporter activity • hydrogen:amino acid symporter activity • L-proline transmembrane transporter activity • glycine transmembrane transporter activity • hydrogen ion transmembrane transporter activity • amino acid transmembrane transporter activity Cellular component • cytoplasm • integral component of membrane • plasma membrane • extracellular exosome • membrane • vacuolar membrane Biological process • proline transmembrane transport • ion transport • amino acid transport • proton transport • glycine transport • L-alanine transport • proline transport • hydrogen ion transmembrane transport • transport Sources:Amigo / QuickGO
Orthologs
Species	Human	Mouse
Entrez	153201	246049
Ensembl	ENSG00000186335	ENSMUSG00000020264
UniProt	Q495M3	Q8BHK3
RefSeq (mRNA)	NM_181776	NM_153170
RefSeq (protein)	NP_861441	NP_694810
Location (UCSC)	Chr 5: 151.31 – 151.35 Mb	Chr 5: 55.16 – 55.19 Mb
PubMed search

153201

246049

ENSG00000186335

ENSMUSG00000020264

Q495M3

Q8BHK3

NM_181776

NM_153170

NP_861441

NP_694810

Solute carrier family 36, member 2 also known as SLC36A2 is a protein which in humans is encoded by the SLC36A2 gene.

SLC36A2 transports small amino acids (glycine, alanine, and proline) and also the D-enantiomers and select amino acid derivatives, such as gamma-aminobutyric acid.

Mutations in the SLC36A2 gene are associated with Iminoglycinuria.

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Wikipedia