GTF2H5

GTF2H5
Available structures
PDBOrtholog search: PDBe RCSB
Identifiers
Aliases GTF2H5, C6orf175, TFB5, TFIIH, TGF2H5, TTD, TTD-A, TTDA, bA120J8.2, TTD3, general transcription factor IIH subunit 5
External IDs MGI: 107227 HomoloGene: 45635 GeneCards: GTF2H5
RNA expression pattern
More reference expression data
Orthologs
Species Human Mouse
Entrez

404672

66467

Ensembl

ENSG00000272047

ENSMUSG00000034345

UniProt

Q6ZYL4

Q8K2X8

RefSeq (mRNA)

NM_207118

NM_181392

RefSeq (protein)

NP_997001.1

NP_852057.2

Location (UCSC) Chr 6: 158.17 – 158.2 Mb Chr 17: 6.08 – 6.09 Mb
PubMed search [1] [2]
Wikidata
View/Edit HumanView/Edit Mouse

General transcription factor IIH subunit 5 is a protein that in humans is encoded by the GTF2H5 gene.[3][4]

Interactions

GTF2H5 has been shown to interact with GTF2H2[3][5] and XPB.[3]

References

  1. "Human PubMed Reference:".
  2. "Mouse PubMed Reference:".
  3. 1 2 3 Giglia-Mari G, Coin F, Ranish JA, Hoogstraten D, Theil A, Wijgers N, Jaspers NG, Raams A, Argentini M, van der Spek PJ, Botta E, Stefanini M, Egly JM, Aebersold R, Hoeijmakers JH, Vermeulen W (June 2004). "A new, tenth subunit of TFIIH is responsible for the DNA repair syndrome trichothiodystrophy group A". Nat. Genet. 36 (7): 714–9. doi:10.1038/ng1387. PMID 15220921.
  4. "Entrez Gene: GTF2H5 general transcription factor IIH, polypeptide 5".
  5. Vermeulen W, Bergmann E, Auriol J, Rademakers S, Frit P, Appeldoorn E, Hoeijmakers JH, Egly JM (November 2000). "Sublimiting concentration of TFIIH transcription/DNA repair factor causes TTD-A trichothiodystrophy disorder". Nat. Genet. 26 (3): 307–13. doi:10.1038/81603. PMID 11062469.

Further reading


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