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    MTCH2 mitochondrial carrier 2 [ Homo sapiens (human) ]

    Gene ID: 23788, updated on 10-Dec-2024

    Summary

    Official Symbol
    MTCH2provided by HGNC
    Official Full Name
    mitochondrial carrier 2provided by HGNC
    Primary source
    HGNC:HGNC:17587
    See related
    Ensembl:ENSG00000109919 MIM:613221; AllianceGenome:HGNC:17587
    Gene type
    protein coding
    RefSeq status
    REVIEWED
    Organism
    Homo sapiens
    Lineage
    Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
    Also known as
    MIMP; HSPC032; SLC25A50
    Summary
    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]
    Expression
    Ubiquitous expression in kidney (RPKM 24.0), testis (RPKM 21.8) and 25 other tissues See more
    Orthologs
    NEW
    Try the new Gene table
    Try the new Transcript table

    Genomic context

    See MTCH2 in Genome Data Viewer
    Location:
    11p11.2
    Exon count:
    14
    Annotation release Status Assembly Chr Location
    RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 11 NC_000011.10 (47604317..47642559, complement)
    RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 11 NC_060935.1 (47764706..47807519, complement)
    RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) 11 NC_000011.9 (47638869..47664111, complement)

    Chromosome 11 - NC_000011.10Genomic Context describing neighboring genes Neighboring gene MPRA-validated peak1274 silencer Neighboring gene MPRA-validated peak1275 silencer Neighboring gene family with sequence similarity 180 member B Neighboring gene C1q and TNF related 4 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 4701 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 3336 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 3337 Neighboring gene AGBL carboxypeptidase 2 Neighboring gene Sharpr-MPRA regulatory region 12296 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 4702 Neighboring gene formin binding protein 4 Neighboring gene H3K27ac hESC enhancer GRCh37_chr11:47787258-47788183 Neighboring gene NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr11:47788184-47789108

    Genomic regions, transcripts, and products

    Bibliography

    GeneRIFs: Gene References Into Functions

    What's a GeneRIF?

    Phenotypes

    EBI GWAS Catalog

    Description
    Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index.
    EBI GWAS Catalog
    Six new loci associated with body mass index highlight a neuronal influence on body weight regulation.
    EBI GWAS Catalog

    HIV-1 interactions

    Protein interactions

    Protein Gene Interaction Pubs
    Vpr vpr HIV-1 Vpr is identified to have a physical interaction with mitochondrial carrier 2 (MTCH2) in human HEK293 and/or Jurkat cell lines by using affinity tagging and purification mass spectrometry analyses PubMed

    Go to the HIV-1, Human Interaction Database

    Interactions

    Products Interactant Other Gene Complex Source Pubs Description

    General gene information

    Markers

    Gene Ontology Provided by GOA

    Function Evidence Code Pubs
    enables membrane insertase activity IDA
    Inferred from Direct Assay
    more info
    PubMed 
    enables protein binding IPI
    Inferred from Physical Interaction
    more info
    PubMed 
    Process Evidence Code Pubs
    involved_in lipid homeostasis ISS
    Inferred from Sequence or Structural Similarity
    more info
     
    involved_in positive regulation of apoptotic process IBA
    Inferred from Biological aspect of Ancestor
    more info
     
    involved_in positive regulation of apoptotic process ISS
    Inferred from Sequence or Structural Similarity
    more info
     
    involved_in positive regulation of stem cell differentiation ISS
    Inferred from Sequence or Structural Similarity
    more info
     
    involved_in protein insertion into mitochondrial outer membrane IDA
    Inferred from Direct Assay
    more info
    PubMed 
    acts_upstream_of_or_within protein localization to mitochondrion IMP
    Inferred from Mutant Phenotype
    more info
    PubMed 
    involved_in regulation of mitochondrial fusion ISS
    Inferred from Sequence or Structural Similarity
    more info
     
    Component Evidence Code Pubs
    located_in membrane HDA PubMed 
    is_active_in membrane IBA
    Inferred from Biological aspect of Ancestor
    more info
     
    is_active_in mitochondrial outer membrane IDA
    Inferred from Direct Assay
    more info
    PubMed 
    located_in mitochondrion HTP PubMed 
    is_active_in mitochondrion IBA
    Inferred from Biological aspect of Ancestor
    more info
     
    located_in nucleus HDA PubMed 

    General protein information

    Preferred Names
    mitochondrial carrier homolog 2
    Names
    met-induced mitochondrial protein
    solute carrier family 25, member 50

    NCBI Reference Sequences (RefSeq)

    NEW Try the new Transcript table

    RefSeqs maintained independently of Annotated Genomes

    These reference sequences exist independently of genome builds. Explain

    These reference sequences are curated independently of the genome annotation cycle, so their versions may not match the RefSeq versions in the current genome build. Identify version mismatches by comparing the version of the RefSeq in this section to the one reported in Genomic regions, transcripts, and products above.

    mRNA and Protein(s)

    1. NM_001317231.2NP_001304160.1  mitochondrial carrier homolog 2 isoform 1x

      Status: REVIEWED

      Description
      Transcript Variant: This variant (1) represents the predominant transcript and encodes two isoforms, which result from the use of alternative in-frame translation termination codons. The shorter isoform (1) results from translation termination at the upstream UGA stop codon, while the longer isoform (1x) results from UGA stop codon readthrough to the downstream UAG termination codon. This RefSeq represents the longer, C-terminally extended isoform (1x). As the UGA stop codon has been reported to specify several alternative amino acids (tryptophan, cysteine, arginine and serine), its location in the longer isoform is denoted by an 'X'.
      Source sequence(s)
      AC104942, AK313032, AY380792
      UniProtKB/TrEMBL
      Q53G34
      Conserved Domains (1) summary
      pfam00153
      Location:128192
      Mito_carr; Mitochondrial carrier protein
    2. NM_001317232.2NP_001304161.1  mitochondrial carrier homolog 2 isoform 2

      Status: REVIEWED

      Description
      Transcript Variant: This variant (2) lacks an in-frame coding exon in the 5' region compared to variant 1. The resulting isoform (2) is shorter, missing an internal protein segment compared to isoform 1.
      Source sequence(s)
      AC104942, AK313032, AY380792, BQ960010
      UniProtKB/TrEMBL
      E9PIE4, Q53G34
      Related
      ENSP00000432043.2, ENST00000530428.2
      Conserved Domains (1) summary
      pfam00153
      Location:119183
      Mito_carr; Mitochondrial carrier protein
    3. NM_001317233.2NP_001304162.1  mitochondrial carrier homolog 2 isoform 3

      Status: REVIEWED

      Description
      Transcript Variant: This variant (3) lacks an exon in the 5' region, which results in translation initiation from an in-frame, downstream start codon compared to variant 1. The encoded isoform (3) has a shorter N-terminus compared to isoform 1.
      Source sequence(s)
      AC104942, AK295218, AK313032, AY380792
      UniProtKB/TrEMBL
      B4DHQ0
      Conserved Domains (1) summary
      pfam00153
      Location:144
      Mito_carr; Mitochondrial carrier protein
    4. NM_014342.4NP_055157.1  mitochondrial carrier homolog 2 isoform 1

      See identical proteins and their annotated locations for NP_055157.1

      Status: REVIEWED

      Description
      Transcript Variant: This variant (1) represents the predominant transcript and encodes two isoforms, which result from the use of alternative in-frame translation termination codons. The shorter isoform (1) results from translation termination at the upstream UGA stop codon, while the longer isoform (1x) results from UGA stop codon readthrough to the downstream UAG termination codon. This RefSeq represents the shorter isoform (1).
      Source sequence(s)
      AC104942, AK313032, AY380792
      Consensus CDS
      CCDS7943.1
      UniProtKB/Swiss-Prot
      B2R7L8, Q9Y6C9
      UniProtKB/TrEMBL
      Q53G34
      Related
      ENSP00000303222.3, ENST00000302503.8
      Conserved Domains (1) summary
      pfam00153
      Location:128192
      Mito_carr; Mitochondrial carrier protein

    RefSeqs of Annotated Genomes: GCF_000001405.40-RS_2024_08

    The following sections contain reference sequences that belong to a specific genome build. Explain

    Reference GRCh38.p14 Primary Assembly

    Genomic

    1. NC_000011.10 Reference GRCh38.p14 Primary Assembly

      Range
      47604317..47642559 complement
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    mRNA and Protein(s)

    1. XM_047426700.1XP_047282656.1  mitochondrial carrier homolog 2 isoform X6

    2. XM_011519960.4XP_011518262.1  mitochondrial carrier homolog 2 isoform X2

      UniProtKB/TrEMBL
      Q53G34
      Conserved Domains (1) summary
      pfam00153
      Location:119183
      Mito_carr; Mitochondrial carrier protein
    3. XM_011519961.3XP_011518263.1  mitochondrial carrier homolog 2 isoform X3

      UniProtKB/TrEMBL
      Q53G34
      Conserved Domains (1) summary
      pfam00153
      Location:128192
      Mito_carr; Mitochondrial carrier protein
    4. XM_011519959.3XP_011518261.1  mitochondrial carrier homolog 2 isoform X1

      UniProtKB/TrEMBL
      Q53G34
      Conserved Domains (1) summary
      pfam00153
      Location:128192
      Mito_carr; Mitochondrial carrier protein
    5. XM_047426701.1XP_047282657.1  mitochondrial carrier homolog 2 isoform X7

      UniProtKB/TrEMBL
      B4DHQ0
    6. XM_017017462.3XP_016872951.1  mitochondrial carrier homolog 2 isoform X5

    7. XM_006718172.3XP_006718235.1  mitochondrial carrier homolog 2 isoform X4

      See identical proteins and their annotated locations for XP_006718235.1

      UniProtKB/TrEMBL
      Q53G34
      Conserved Domains (1) summary
      pfam00153
      Location:128192
      Mito_carr; Mitochondrial carrier protein

    Reference GRCh38.p14 PATCHES

    Genomic

    1. NW_019805496.1 Reference GRCh38.p14 PATCHES

      Range
      32135..74925 complement
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    mRNA and Protein(s)

    1. XM_054332416.1XP_054188391.1  mitochondrial carrier homolog 2 isoform X2

      UniProtKB/TrEMBL
      Q53G34
    2. XM_054332417.1XP_054188392.1  mitochondrial carrier homolog 2 isoform X3

      UniProtKB/TrEMBL
      Q53G34
    3. XM_054332415.1XP_054188390.1  mitochondrial carrier homolog 2 isoform X1

      UniProtKB/TrEMBL
      Q53G34
    4. XM_054332420.1XP_054188395.1  mitochondrial carrier homolog 2 isoform X6

    5. XM_054332419.1XP_054188394.1  mitochondrial carrier homolog 2 isoform X5

    6. XM_054332418.1XP_054188393.1  mitochondrial carrier homolog 2 isoform X4

      UniProtKB/TrEMBL
      Q53G34
    7. XM_054332421.1XP_054188396.1  mitochondrial carrier homolog 2 isoform X7

      UniProtKB/TrEMBL
      B4DHQ0

    Alternate T2T-CHM13v2.0

    Genomic

    1. NC_060935.1 Alternate T2T-CHM13v2.0

      Range
      47764706..47807519 complement
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    mRNA and Protein(s)

    1. XM_054368274.1XP_054224249.1  mitochondrial carrier homolog 2 isoform X2

      UniProtKB/TrEMBL
      Q53G34
    2. XM_054368275.1XP_054224250.1  mitochondrial carrier homolog 2 isoform X3

      UniProtKB/TrEMBL
      Q53G34
    3. XM_054368273.1XP_054224248.1  mitochondrial carrier homolog 2 isoform X1

      UniProtKB/TrEMBL
      Q53G34
    4. XM_054368278.1XP_054224253.1  mitochondrial carrier homolog 2 isoform X6

    5. XM_054368277.1XP_054224252.1  mitochondrial carrier homolog 2 isoform X5

    6. XM_054368276.1XP_054224251.1  mitochondrial carrier homolog 2 isoform X4

      UniProtKB/TrEMBL
      Q53G34
    7. XM_054368279.1XP_054224254.1  mitochondrial carrier homolog 2 isoform X7

      UniProtKB/TrEMBL
      B4DHQ0