Solute carrier family 38 member 9

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

Solute carrier family 38 member 9 is a protein that in humans is encoded by the SLC38A9 gene.[5]

AliasesSLC38A9, URLC11, solute carrier family 38 member 9
End55,773,194 bp[1]
Quick facts SLC38A9, Identifiers ...
SLC38A9
Identifiers
AliasesSLC38A9, URLC11, solute carrier family 38 member 9
External IDsOMIM: 616203; MGI: 1918839; HomoloGene: 18139; GeneCards: SLC38A9; OMA:SLC38A9 - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_175376
NM_178746

RefSeq (protein)

NP_848861

Location (UCSC)Chr 5: 55.63 – 55.77 MbChr 13: 112.8 – 112.88 Mb
PubMed search[3][4]
Wikidata
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