MTCH2
Sign in to saveAlso known as MIMP, SLC25A50, HSPC032, mitochondrial carrier 2
Mitochondrial carrier homolog 2 also known as MTCH2 is a protein which in humans is encoded by the MTCH2 gene.
Gene data
MTCH2- Name
- mitochondrial carrier 2
- Type
- protein-coding
- Aliases
- HSPC032, MIMP, SLC25A50
This gene encodes a member of the SLC25 family of nuclear-encoded transporters that are localized in the inner mitochondrial membrane. Members of this superfamily are involved in many metabolic pathways and cell functions. Genome-wide association studies in human have identified single-nucleotide polymorphisms in several loci associated with obesity. This gene is one such locus, which is highly expressed in white adipose tissue and adipocytes, and thought to play a regulatory role in adipocyte differentiation and biology. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. A recent study showed this gene to be an authentic stop codon readthrough target that can produce two isoforms from the same mRNA by use of alternative in-frame translation termination codons. [provided by RefSeq, Dec 2017].
via MyGene.info
Gene · Ensembl
mitochondrial carrier 2
- Symbol
- MTCH2
- Biotype
- Protein coding
- Organism
- Homo sapiens
- Location
- 11:47,604,339-47,642,698
- Strand
- Reverse (−)
- Assembly
- GRCh38
via Ensembl · EMBL-EBI
Wikidata facts
Show 5 more facts
- HomoloGene ID
- 8645
- exact match
- identifiers.org/ncbigene/23788
- genomic end
- 47642607
- genomic start
- 47638867
- cytogenetic location
- 11p11.2
Sources (4)
via Wikidata · CC0
~1 min read
Article
4 sectionsContents
- Clinical significance
- See also
- References
- Further reading
Mitochondrial carrier homolog 2 also known as MTCH2 is a protein which in humans is encoded by the MTCH2 gene.
MTCH2 resides on the outer mitochondrial membrane where it co-localizes with the apoptotic Bcl-2 family protein BID.