SLC2A13
Sign in to saveAlso known as HMIT, solute carrier family 2 member 13
'Proton myo-inositol cotransporter, also known as solute carrier family 2 member 13' is a protein that in humans is encoded by the SLC2A13 gene.
Gene data
SLC2A13- Name
- solute carrier family 2 member 13
- Type
- protein-coding
- Position
- 39,755,025–40,106,089 (−)
- Aliases
- HMIT
- Ensembl
- ENSG00000151229
- RefSeq RNA
- NM_052885.4, XM_011537847.3, XM_011537849.3, XM_011537850.4, XM_017018764.2
- RefSeq protein
- NP_443117.3, XP_011536149.1, XP_011536151.1, XP_011536152.1, XP_016874253.1
Enables ATPase binding activity; myo-inositol:proton symporter activity; and protease binding activity. Involved in myo-inositol transport and positive regulation of amyloid-beta formation. Is integral component of plasma membrane. Part of cell body; cell periphery; and cell projection. [provided by Alliance of Genome Resources, Apr 2022]
Gene Ontology
Biological process
Molecular function
Pathways
via MyGene.info
Gene · Ensembl
solute carrier family 2 member 13
- Symbol
- SLC2A13
- Biotype
- Protein coding
- Organism
- Homo sapiens
- Location
- 12:39,755,025-40,106,094
- Strand
- Reverse (−)
- Assembly
- GRCh38
via Ensembl · EMBL-EBI
Wikidata facts
Show 5 more facts
- HomoloGene ID
- 43139
- exact match
- identifiers.org/ncbigene/114134
- genomic end
- 40499891
- genomic start
- 39755025
- cytogenetic location
- 12q12
via Wikidata · CC0
~1 min read
Article
2 sectionsContents
- References
- Further reading
'Proton myo-inositol cotransporter, also known as solute carrier family 2 member 13' is a protein that in humans is encoded by the SLC2A13 gene.
== References ==