MTCH2
Mitochondrial carrier homolog 2
Also known as: MTCH2_HUMAN, SLC25A50
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q9Y6C9
- Gene
- MTCH2
- Ensembl
- ENSG00000109919
- Chromosome
- 11
- Canonical length
- 303 aa
- Protein class
- Predicted membrane proteins, Transporters
- Subcellular location
- Mitochondria
OverviewNCBI Gene
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]
Canonical amino-acid sequenceUniProt
303 residues, UniProt reviewed canonical sequence.
>Q9Y6C9|MTCH2
1 MADAASQVLL GSGLTILSQP LMYVKVLIQV GYEPLPPTIG RNIFGRQVCQ LPGLFSYAQH
61 IASIDGRRGL FTGLTPRLCS GVLGTVVHGK VLQHYQESDK GEELGPGNVQ KEVSSSFDHV
121 IKETTREMIA RSAATLITHP FHVITLRSMV QFIGRESKYC GLCDSIITIY REEGILGFFA
181 GLVPRLLGDI LSLWLCNSLA YLVNTYALDS GVSTMNEMKS YSQAVTGFFA SMLTYPFVLV
241 SNLMAVNNCG LAGGCPPYSP IYTSWIDCWC MLQKEGNMSR GNSLFFRKVP FGKTYCCDLK
301 MLILocalizationUniProt · AlphaFold · HPA
Whether an antibody against MTCH2 can act on the native protein depends on physical access: surface and secreted proteins are reachable by circulating antibodies, intracellular proteins usually are not.
- Antibody reachability
- Other membrane
- Secreted
- No
- Transmembrane segments
- 6
- Mean surface accessibility (rSASA)
- 0.32
- Highest tissue expression
- 108 nTPM
Expression across tissuesHPA
Tissue
- liver: 108 nTPM
- skeletal muscle: 76 nTPM
- testis: 66 nTPM
- kidney: 54 nTPM
- esophagus: 47 nTPM
- tongue: 44 nTPM
Single-cell type
- late primary spermatocytes: 726 nCPM
- early spermatids: 505 nCPM
- gastric progenitor cells: 294 nCPM
- early primary spermatocytes: 205 nCPM
- hepatocytes: 201 nCPM
- esophageal suprabasal cells: 171 nCPM
Immune cell
- myeloid DC: 44 nTPM
- intermediate monocyte: 38 nTPM
- total PBMC: 34 nTPM
- classical monocyte: 34 nTPM
- non-classical monocyte: 32 nTPM
- plasmacytoid DC: 29 nTPM
Brain region
- hypothalamus: 24 nTPM
- thalamus: 24 nTPM
- white matter: 23 nTPM
- cerebellum: 22 nTPM
- midbrain: 22 nTPM
- basal ganglia: 22 nTPM
Genetic constraint and essentialitygnomAD · DepMap
Does the body need this protein intact? Low LOEUF or a strong DepMap dependency means loss or blockade of the protein is likely to be felt.
- gnomAD LOEUF (loss-of-function intolerance)
- 0.56
- gnomAD pLI
- 0.03
- gnomAD missense Z
- 1.2
- DepMap mean gene effect
- -0.17
- DepMap dependency class
- selective
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 5% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- cellular response to radiation
- establishment of protein localization to mitochondrial membrane involved in mitochondrial fission
- hematopoietic stem cell homeostasis
- hematopoietic stem cell migration
- hepatocyte apoptotic process
- lactate metabolic process
- lipid homeostasis
- mitochondrial ATP synthesis coupled electron transport
- negative regulation of glycolytic process
- negative regulation of mitochondrial membrane potential
- positive regulation of apoptotic process
- positive regulation of intrinsic apoptotic signaling pathway in response to DNA damage
- positive regulation of stem cell differentiation
- protein insertion into mitochondrial outer membrane
- protein localization to mitochondrion
- regulation of mitochondrial fusion
- regulation of mitochondrial membrane permeability involved in apoptotic process
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of MTCH2 in the human serome: UniProt-annotated complex subunits plus reported interactors. Each links to its own Seroatlas record.
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads MTCH2 as an antibody target. Whether an autoantibody or antibody against MTCH2 could matter depends on whether native MTCH2 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
MTCH2 is annotated as predominantly intracellular. Intracellular proteins are common autoantibody markers, becoming visible to the immune system after cell injury or altered processing, but are usually markers of disease rather than direct drivers.
Annotation status
The present source text does not explicitly label MTCH2 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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