SLC2A13

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

114134

239606

Ensembl

ENSG00000151229

ENSMUSG00000036298

UniProt

Q96QE2

Q3UHK1

RefSeq (mRNA)

NM_052885

NM_001033633

RefSeq (protein)

NP_443117.3

NP_001028805.2

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

Further reading


This article is issued from Wikipedia - version of the 5/20/2016. The text is available under the Creative Commons Attribution/Share Alike but additional terms may apply for the media files.