SLC2A13

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SLC2A13
Identifiers
Aliases SLC2A13, HMIT, solute carrier family 2 member 13
External IDs MGI: 2146030 HomoloGene: 43139 GeneCards: SLC2A13
Genetically Related Diseases
Parkinson's disease[1]
Orthologs
Species Human Mouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_052885

NM_001033633

RefSeq (protein)

NP_443117

NP_001028805.2
NP_001028805

Location (UCSC) Chr 12: 39.76 – 40.11 Mb Chr 15: 91.27 – 91.57 Mb
PubMed search [2] [3]
Wikidata
View/Edit Human View/Edit Mouse

Solute carrier family 2 (facilitated glucose transporter), member 13 is a protein that in humans is encoded by the SLC2A13 gene.[4]

References[edit]

Further reading[edit]