TIMM9

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

Mitochondrial import inner membrane translocase subunit Tim9 is an enzyme that in humans is encoded by the TIMM9 gene.[5][6][7]

PDBOrtholog search: PDBe RCSB
AliasesTIMM9, TIM9, TIM9A, translocase of inner mitochondrial membrane 9
Quick facts Available structures, PDB ...
TIMM9
Available structures
PDBOrtholog search: PDBe RCSB
Identifiers
AliasesTIMM9, TIM9, TIM9A, translocase of inner mitochondrial membrane 9
External IDsOMIM: 607384; MGI: 1353436; HomoloGene: 40847; GeneCards: TIMM9; OMA:TIMM9 - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_001024853
NM_001024854
NM_001286203
NM_013896

RefSeq (protein)

NP_001020024
NP_001020025
NP_001273132
NP_038924

Location (UCSC)Chr 14: 58.41 – 58.43 MbChr 12: 71.17 – 71.18 Mb
PubMed search[3][4]
Wikidata
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TIMM9 belongs to a family of evolutionarily conserved proteins that are organized in heterooligomeric complexes in the mitochondrial intermembrane space.

These proteins mediate the import and insertion of hydrophobic membrane proteins into the mitochondrial inner membrane.[supplied by OMIM][7]

References

Further reading

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