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TIMM9

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Protein-coding gene in the species Homo sapiens
TIMM9
Available structures
PDBOrtholog search: PDBe RCSB
List of PDB id codes

2BSK

Identifiers
AliasesTIMM9, TIM9, TIM9A, translocase of inner mitochondrial membrane 9
External IDsOMIM: 607384; MGI: 1353436; HomoloGene: 40847; GeneCards: TIMM9; OMA:TIMM9 - orthologs
Gene location (Human)
Chromosome 14 (human)
Chr.Chromosome 14 (human)
Chromosome 14 (human)Genomic location for TIMM9Genomic location for TIMM9
Band14q23.1Start58,408,495 bp
End58,427,531 bp
Gene location (Mouse)
Chromosome 12 (mouse)
Chr.Chromosome 12 (mouse)
Chromosome 12 (mouse)Genomic location for TIMM9Genomic location for TIMM9
Band12 C2|12Start71,169,947 bp
End71,183,458 bp
RNA expression pattern
Bgee
HumanMouse (ortholog)
Top expressed in
  • body of pancreas

  • ganglionic eminence

  • muscle of thigh

  • epithelium of colon

  • ventricular zone

  • gastrocnemius muscle

  • left ovary

  • gonad

  • muscle layer of sigmoid colon

  • right ovary
Top expressed in
  • primary oocyte

  • right kidney

  • embryo

  • secondary oocyte

  • embryo

  • blastocyst

  • proximal tubule

  • yolk sac

  • dentate gyrus of hippocampal formation granule cell

  • superior frontal gyrus
More reference expression data
BioGPS
More reference expression data
Gene ontology
Molecular function
Cellular component
Biological process
Sources:Amigo / QuickGO
Orthologs
SpeciesHumanMouse
Entrez

26520

30056

Ensembl

ENSG00000100575

ENSMUSG00000021079

UniProt

Q9Y5J7

Q9WV98

RefSeq (mRNA)
NM_001304485
NM_001304486
NM_001304487
NM_001304488
NM_001304489

NM_001304490
NM_001304491
NM_012460

NM_001024853
NM_001024854
NM_001286203
NM_013896

RefSeq (protein)
NP_001291414
NP_001291415
NP_001291416
NP_001291417
NP_001291418

NP_001291419
NP_001291420
NP_036592

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
Wikidata
View/Edit HumanView/Edit Mouse

Mitochondrial import inner membrane translocase subunit Tim9 is an enzyme that in humans is encoded by the TIMM9 gene.

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.

References

  1. ^ GRCh38: Ensembl release 89: ENSG00000100575Ensembl, May 2017
  2. ^ GRCm38: Ensembl release 89: ENSMUSG00000021079Ensembl, May 2017
  3. "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  4. "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  5. Jin H, Kendall E, Freeman TC, Roberts RG, Vetrie DL (Feb 2000). "The human family of Deafness/Dystonia peptide (DDP) related mitochondrial import proteins". Genomics. 61 (3): 259–67. doi:10.1006/geno.1999.5966. PMID 10552927.
  6. Muhlenbein N, Hofmann S, Rothbauer U, Bauer MF (Mar 2004). "Organization and function of the small Tim complexes acting along the import pathway of metabolite carriers into mammalian mitochondria". J Biol Chem. 279 (14): 13540–6. doi:10.1074/jbc.M312485200. PMID 14726512.
  7. ^ "Entrez Gene: TIMM9 translocase of inner mitochondrial membrane 9 homolog (yeast)".

Further reading

PDB gallery
  • 2bsk: CRYSTAL STRUCTURE OF THE TIM9 TIM10 HEXAMERIC COMPLEX 2bsk: CRYSTAL STRUCTURE OF THE TIM9 TIM10 HEXAMERIC COMPLEX


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