IFT80, intraflagellar transport 80

IFT80, intraflagellar transport 80

• The protein encoded by this gene is part of the intraflagellar transport complex B and is necessary for the function of motile and sensory cilia. Defects in this gene are a cause of asphyxiating thoracic dystrophy 2 (ATD2). Three transcript variants encoding two different isoforms have been found for this gene.[provided by RefSeq, Jun 2010]

• Gene Synonyms (ATD2, FAP167, SRTD2, WDR56, intraflagellar transport protein 80 homolog, WD repeat domain 56, WD repeat-containing protein 56, intraflagellar transport 80 homolog,)
• NCBI Gene ID: 57560
• Species: Homo sapiens (Human)
• UNIPROT ID#>>Q9P2H3
• View the NCBI Database for this Gene »

Gene products are often involved in multiple pathways and networks within a living cell. Learn more about other interacting partners.

intraflagellar transport 80 interacts with:

• intraflagellar transport 20
  intraflagellar transport 22
  intraflagellar transport 74
  lebercilin LCA5
  tetratricopeptide repeat domain 26
  tetratricopeptide repeat domain 30A
  tetratricopeptide repeat domain 30B
  UBX domain protein 10
  zinc finger containing ubiquitin peptidase 1

Paste a protein or nucleic acid sequence in the box below to confirm that it matches this gene’s reference sequence(s). Click on a link under RELATED ORF CLONES to see how a sequence matches to an experimentally-validated ORF clone.