SLC2A6

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

Solute carrier family 2, facilitated glucose transporter member 6 is a protein that in humans is encoded by the SLC2A6 gene.[5][6]

AliasesSLC2A6, GLUT6, GLUT9, HSA011372, solute carrier family 2 member 6
End133,479,127 bp[1]
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SLC2A6
Identifiers
AliasesSLC2A6, GLUT6, GLUT9, HSA011372, solute carrier family 2 member 6
External IDsOMIM: 606813; MGI: 2443286; HomoloGene: 69236; GeneCards: SLC2A6; OMA:SLC2A6 - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_001145099
NM_017585

NM_001177627
NM_172659

RefSeq (protein)

NP_001138571
NP_060055

NP_001171098
NP_766247

Location (UCSC)Chr 9: 133.47 – 133.48 MbChr 2: 26.91 – 26.92 Mb
PubMed search[3][4]
Wikidata
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Function

Hexose transport into mammalian cells is catalyzed by a family of membrane proteins, including SLC2A6, that contain 12 transmembrane domains and a number of critical conserved residues.[supplied by OMIM][6]

See also

References

Further reading

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