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.
In the Vinony graph
Within Vinony's link graph, SLC2A13 is referenced by 257 other articles, and connects out to PubMed, human chromosome 12 and transmembrane transport proteins.
It is catalogued under topics including Genes on human chromosome 12 and Solute carrier family.
Its subject is documented across 6 Wikipedia language editions.
Gene data
SLC2A13- Name
- solute carrier family 2 member 13
- Type
- protein-coding
- Position
- 39,755,025–40,106,094 (−)
- 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
- Instance of
- gene
Show 9 more facts
- HomoloGene ID
- 43139
- genetic association
- Parkinson's disease
- found in taxon
- Homo sapiens
- exact match
- identifiers.org/ncbigene/114134
- genomic end
- 40499891
- genomic start
- 39755025
- chromosome
- human chromosome 12
- cytogenetic location
- 12q12
- expressed in
- middle temporal gyrus
via Wikidata · CC0
~1 min read
Encyclopedic overview
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 ==
Excerpted from Wikipedia’s “SLC2A13” article, available under the CC BY-SA 4.0 licence.