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Mtch2 mitochondrial carrier 2 [ Rattus norvegicus (Norway rat) ]

Gene ID: 295922, updated on 27-Nov-2024

Summary

Official Symbol
Mtch2provided by RGD
Official Full Name
mitochondrial carrier 2provided by RGD
Primary source
RGD:1308080
See related
EnsemblRapid:ENSRNOG00000058658 AllianceGenome:RGD:1308080
Gene type
protein coding
RefSeq status
REVIEWED
Organism
Rattus norvegicus
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Glires; Rodentia; Myomorpha; Muroidea; Muridae; Murinae; Rattus
Also known as
Hspc032
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. 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
Biased expression in Liver (RPKM 800.2), Heart (RPKM 701.8) and 9 other tissues See more
Orthologs
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Genomic context

See Mtch2 in Genome Data Viewer
Location:
3q24
Exon count:
13
Annotation release Status Assembly Chr Location
RS_2024_02 current GRCr8 (GCF_036323735.1) 3 NC_086021.1 (97286388..97306028)
RS_2023_06 previous assembly mRatBN7.2 (GCF_015227675.2) 3 NC_051338.1 (76830549..76850189)
106 previous assembly Rnor_6.0 (GCF_000001895.5) 3 NC_005102.4 (79678141..79695356)

Chromosome 3 - NC_086021.1Genomic Context describing neighboring genes Neighboring gene formin binding protein 4 Neighboring gene AGBL carboxypeptidase 2 Neighboring gene ribosomal protein S26, pseudogene 9 Neighboring gene C1q and TNF related 4 Neighboring gene family with sequence similarity 180 member B

Genomic regions, transcripts, and products

Expression

  • Project title: A rat RNA-Seq transcriptomic BodyMap across 11 organs and 4 developmental stages
  • Description: 320 RNA samples isolated from 11 organs (adrenal gland, brain, heart, kidney, liver, lung, muscle, spleen, thymus, and testes or uterus) from both sexes of Fischer 344 rats across four developmental stages (2-, 6-, 21-, and 104-weeks-old)
  • BioProject: PRJNA238328
  • Publication: PMID 24510058
  • Analysis date: Mon Jun 6 17:44:12 2016

Interactions

Products Interactant Other Gene Complex Source Pubs Description

General gene information

Markers

Gene Ontology Provided by RGD

Function Evidence Code Pubs
enables membrane insertase activity ISO
Inferred from Sequence Orthology
more info
 
Process Evidence Code Pubs
acts_upstream_of_or_within cellular response to radiation ISO
Inferred from Sequence Orthology
more info
 
acts_upstream_of_or_within establishment of protein localization to mitochondrial membrane involved in mitochondrial fission ISO
Inferred from Sequence Orthology
more info
 
acts_upstream_of_or_within hematopoietic stem cell homeostasis ISO
Inferred from Sequence Orthology
more info
 
acts_upstream_of_or_within hematopoietic stem cell migration ISO
Inferred from Sequence Orthology
more info
 
acts_upstream_of_or_within hepatocyte apoptotic process ISO
Inferred from Sequence Orthology
more info
 
acts_upstream_of_or_within lactate metabolic process ISO
Inferred from Sequence Orthology
more info
 
involved_in lipid homeostasis ISO
Inferred from Sequence Orthology
more info
 
acts_upstream_of_or_within mitochondrial ATP synthesis coupled electron transport ISO
Inferred from Sequence Orthology
more info
 
acts_upstream_of_or_within negative regulation of glycolytic process ISO
Inferred from Sequence Orthology
more info
 
acts_upstream_of_or_within negative regulation of mitochondrial membrane potential ISO
Inferred from Sequence Orthology
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 ISO
Inferred from Sequence Orthology
more info
 
acts_upstream_of_or_within positive regulation of intrinsic apoptotic signaling pathway in response to DNA damage ISO
Inferred from Sequence Orthology
more info
 
involved_in positive regulation of stem cell differentiation ISO
Inferred from Sequence Orthology
more info
 
involved_in protein insertion into mitochondrial outer membrane ISO
Inferred from Sequence Orthology
more info
 
acts_upstream_of_or_within protein localization to mitochondrion ISO
Inferred from Sequence Orthology
more info
 
involved_in regulation of mitochondrial fusion ISO
Inferred from Sequence Orthology
more info
 
acts_upstream_of_or_within regulation of mitochondrial membrane permeability involved in apoptotic process ISO
Inferred from Sequence Orthology
more info
 
Component Evidence Code Pubs
is_active_in membrane IBA
Inferred from Biological aspect of Ancestor
more info
 
is_active_in mitochondrial outer membrane ISO
Inferred from Sequence Orthology
more info
 
located_in mitochondrial outer membrane ISO
Inferred from Sequence Orthology
more info
 
is_active_in mitochondrion IBA
Inferred from Biological aspect of Ancestor
more info
 
located_in mitochondrion ISO
Inferred from Sequence Orthology
more info
PubMed 

General protein information

Preferred Names
mitochondrial carrier homolog 2

NCBI Reference Sequences (RefSeq)

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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_001106488.3NP_001099958.2  mitochondrial carrier homolog 2 isoform 1

    See identical proteins and their annotated locations for NP_001099958.2

    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)
    BC158687, BP503204, CB758525, DY315983, EV779017, FM085474, FM112089, FM132670
    UniProtKB/TrEMBL
    A0A0E3DAF7, A0A8I6ACP2, B0BN52
    Related
    ENSRNOP00000074292.2, ENSRNOT00000087604.3
    Conserved Domains (1) summary
    pfam00153
    Location:128192
    Mito_carr; Mitochondrial carrier protein
  2. NM_001317330.1NP_001304259.1  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)
    BC158687, BP503204, CB758525, DY315983, EV779017, FM085474, FM112089, FM132670
    UniProtKB/TrEMBL
    A0A8I6ACP2
    Conserved Domains (1) summary
    pfam00153
    Location:128192
    Mito_carr; Mitochondrial carrier protein

RefSeqs of Annotated Genomes: GCF_036323735.1-RS_2024_02

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

Reference GRCr8

Genomic

  1. NC_086021.1 Reference GRCr8

    Range
    97286388..97306028
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)