IFT80

From Wikipedia, the free encyclopedia
Jump to navigation Jump to search

Lua error in Module:Infobox_gene at line 53: attempt to index field 'wikibase' (a nil value). 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.[1][2]

Function

[edit | edit source]

IFT80 is part of the intraflagellar transport complex B and is necessary for the function of motile and sensory cilia.[1]

Clinical significance

[edit | edit source]

Mutations in the IFT80 gene are associated with asphyxiating thoracic dysplasia.[2]

References

[edit | edit source]
  1. ^ a b Lua error in Module:Citation/CS1/Configuration at line 2172: attempt to index field '?' (a nil value).
  2. ^ a b Lua error in Module:Citation/CS1/Configuration at line 2172: attempt to index field '?' (a nil value).

Further reading

[edit | edit source]
  • Lua error in Module:Citation/CS1/Configuration at line 2172: attempt to index field '?' (a nil value).
  • Lua error in Module:Citation/CS1/Configuration at line 2172: attempt to index field '?' (a nil value).
  • Lua error in Module:Citation/CS1/Configuration at line 2172: attempt to index field '?' (a nil value).
  • Lua error in Module:Citation/CS1/Configuration at line 2172: attempt to index field '?' (a nil value).
  • Lua error in Module:Citation/CS1/Configuration at line 2172: attempt to index field '?' (a nil value).

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