IFT52, intraflagellar transport 52

IFT52, intraflagellar transport 52

• This gene encodes a conserved proline-rich protein that is a component of the intraflagellar transport-B (IFT-B) core complex. The encoded protein is essential for the integrity of the IFT-B core complex, and for biosynthesis and maintenance of cilia. Mutations in this gene are associated with ciliopathy that affects the skeleton. [provided by RefSeq, Oct 2016]

• Gene Synonyms (intraflagellar transport protein 52 homolog, protein NGD5 homolog, C20orf9, CGI-53, NGD2, NGD5,)
• NCBI Gene ID: 51098
• Species: Homo sapiens (Human)
• UNIPROT ID#>>Q9Y366
• 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 52 interacts with:

• ADP ribosylation factor like GTPase 13B
  ankyrin repeat domain 55
  family with sequence similarity 210 member A
  heat shock protein family B (small) member 11
  intraflagellar transport 20
  intraflagellar transport 22
  intraflagellar transport 46
  intraflagellar transport 57
  intraflagellar transport 74
  intraflagellar transport 80
  leucine rich repeat containing 27
  solute carrier family 35 member E1
  tetratricopeptide repeat domain 26
  tetratricopeptide repeat domain 30A
  tetratricopeptide repeat domain 30B
  UBX domain protein 10

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.