IFT80
Identifiers
AliasesIFT80, ATD2, SRTD2, WDR56, intraflagellar transport 80, FAP167
External IDsOMIM: 611177 MGI: 1915509 HomoloGene: 12253 GeneCards: IFT80
Orthologs
SpeciesHumanMouse
Entrez

57560

68259

Ensembl

ENSG00000068885

ENSMUSG00000027778

UniProt

Q9P2H3

Q8K057

RefSeq (mRNA)

NM_020800
NM_001190241
NM_001190242

NM_026641

RefSeq (protein)

NP_001177170
NP_001177171
NP_065851

NP_080917

Location (UCSC)Chr 3: 160.26 – 160.4 MbChr 3: 68.8 – 68.91 Mb
PubMed search[3][4]
Wikidata
View/Edit HumanView/Edit Mouse

Intraflagellar transport protein 80 homolog (IFT80), also known as WD repeat-containing protein 56, is a protein that in humans is encoded by the IFT80 gene.[5][6]

Function

IFT80 is part of the intraflagellar transport complex B and is necessary for the function of motile and sensory cilia.[5]

Clinical significance

Mutations in the IFT80 gene are associated with asphyxiating thoracic dysplasia.[6]

References

  1. ^ a b c GRCh38: Ensembl release 89: ENSG00000068885 - Ensembl, May 2017
  2. ^ a b c GRCm38: Ensembl release 89: ENSMUSG00000027778 - Ensembl, 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. ^ a b "Entrez Gene: intraflagellar transport 80 homolog (Chlamydomonas)".
  6. ^ a b Beales PL, Bland E, Tobin JL, Bacchelli C, Tuysuz B, Hill J, Rix S, Pearson CG, Kai M, Hartley J, Johnson C, Irving M, Elcioglu N, Winey M, Tada M, Scambler PJ (June 2007). "IFT80, which encodes a conserved intraflagellar transport protein, is mutated in Jeune asphyxiating thoracic dystrophy". Nat. Genet. 39 (6): 727–9. doi:10.1038/ng2038. PMID 17468754. S2CID 8920064.

Further reading

This article incorporates text from the United States National Library of Medicine, which is in the public domain.



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