IFT43, intraflagellar transport 43

IFT43, intraflagellar transport 43

• This gene encodes a subunit of the intraflagellar transport complex A (IFT-A). IFT-A is a multiprotein complex that plays an important role in cilia assembly and maintenance by mediating retrograde ciliary transport. Mutations in this gene are a cause of cranioectodermal dysplasia-3 (CED3), also known as Sensenbrenner syndrome. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Dec 2011]

• Gene Synonyms (C14orf179, CED3, RP81, SRTD18, intraflagellar transport protein 43 homolog, IFT complex A subunit, intraflagellar transport 43 homolog,)
• NCBI Gene ID: 112752
• Species: Homo sapiens (Human)
• UNIPROT ID#>>Q96FT9
  UNIPROT ID#>>A0A024R6A9
• 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 43 interacts with:

• intraflagellar transport associated protein
  SUMO peptidase family member, NEDD8 specific

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.