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TIMM10B

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Protein-coding gene in the species Homo sapiens
TIMM10B
Available structures
PDBOrtholog search: PDBe RCSB
List of PDB id codes

2BSK

Identifiers
AliasesTIMM10B, FXC1, TIM10B, Tim9b, translocase of inner mitochondrial membrane 10 homolog B (yeast), translocase of inner mitochondrial membrane 10B
External IDsOMIM: 607388; MGI: 1315196; HomoloGene: 8142; GeneCards: TIMM10B; OMA:TIMM10B - orthologs
Gene location (Human)
Chromosome 11 (human)
Chr.Chromosome 11 (human)
Chromosome 11 (human)Genomic location for TIMM10BGenomic location for TIMM10B
Band11p15.4Start6,481,501 bp
End6,484,681 bp
Gene location (Mouse)
Chromosome 7 (mouse)
Chr.Chromosome 7 (mouse)
Chromosome 7 (mouse)Genomic location for TIMM10BGenomic location for TIMM10B
Band7|7 E3Start105,640,056 bp
End105,643,637 bp
RNA expression pattern
Bgee
HumanMouse (ortholog)
Top expressed in
  • secondary oocyte

  • tibia

  • sperm

  • gonad

  • saphenous vein

  • epithelium of colon

  • superior vestibular nucleus

  • spinal ganglia

  • ventral tegmental area

  • amniotic fluid
Top expressed in
  • granulocyte

  • right kidney

  • embryo

  • embryo

  • muscle of thigh

  • lip

  • ventricular zone

  • superior frontal gyrus

  • yolk sac

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

26515

14356

Ensembl

ENSG00000132286

ENSMUSG00000089847

UniProt

Q9Y5J6

Q9WV96

RefSeq (mRNA)

NM_012192

NM_019502

RefSeq (protein)

NP_036324

NP_062375
NP_001346981
NP_001346982
NP_001346983
NP_001346984

NP_001346985
NP_001346987
NP_001346988
NP_001346989
NP_001346990

Location (UCSC)Chr 11: 6.48 – 6.48 MbChr 7: 105.64 – 105.64 Mb
PubMed search
Wikidata
View/Edit HumanView/Edit Mouse

Mitochondrial import inner membrane translocase subunit Tim9 B is an enzyme that in humans is encoded by the FXC1 gene.

FXC1, or TIMM10B, 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: ENSG00000132286Ensembl, May 2017
  2. ^ GRCm38: Ensembl release 89: ENSMUSG00000089847Ensembl, 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. ^ "Entrez Gene: FXC1 fracture callus 1 homolog (rat)".

Further reading


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