TIMM13

Protein-coding gene in the species Homo sapiens From Wikipedia, the free encyclopedia

Mitochondrial import inner membrane translocase subunit Tim13 is an enzyme that in humans is encoded by the TIMM13 gene.[5][6][7]

AliasesTIMM13, TIM13, TIM13B, TIMM13A, TIMM13B, ppv1, translocase of inner mitochondrial membrane 13
End2,427,586 bp[1]
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TIMM13
Identifiers
AliasesTIMM13, TIM13, TIM13B, TIMM13A, TIMM13B, ppv1, translocase of inner mitochondrial membrane 13
External IDsOMIM: 607383; MGI: 1353432; HomoloGene: 40846; GeneCards: TIMM13; OMA:TIMM13 - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_012458

NM_013895

RefSeq (protein)

NP_036590

NP_038923

Location (UCSC)Chr 19: 2.43 – 2.43 MbChr 10: 80.74 – 80.74 Mb
PubMed search[3][4]
Wikidata
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Function

This gene encodes a translocase with similarity to yeast mitochondrial proteins that are involved in the import of metabolite transporters from the cytoplasm and into the mitochondrial inner membrane. The encoded protein and the TIMM8a protein form a 70 kDa complex in the intermembrane space. This gene is in a head-to-tail orientation with the gene for lamin B2.[7]

Interactions

TIMM13 has been shown to interact with TIMM8A.[8][9]

References

Further reading

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