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IFT88, intraflagellar transport 88

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IFT88, intraflagellar transport 88

  • This gene encodes a member of the tetratrico peptide repeat (TPR) family. The encoded protein is involved in cilium biogenesis. Mutations of a similar gene in mouse can cause polycystic kidney disease. Several transcript variants encoding distinct isoforms have been identified for this gene. [provided by RefSeq, Jul 2017]

  • Gene Synonyms (intraflagellar transport protein 88 homolog, TPR repeat protein 10, intraflagellar transport 88 homolog, polaris homolog, probe hTg737 (polycystic kidney disease, autosomal recessive), recessive polycystic kidney disease protein Tg737 homolog, testicular tissue protein Li 93, tetratricopeptide repeat domain 10, tetratricopeptide repeat protein 10, D13S1056E, DAF19, TG737, TTC10, hTg737,)
  • NCBI Gene ID: 8100
  • Species: Homo sapiens (Human)
  • UNIPROT ID#>>A0A140VJL7
    UNIPROT ID#>>B3KX42
    UNIPROT ID#>>Q13099
  • View the NCBI Database for this Gene »

The information on this page was collected from publicly accessible databases, and is periodically updated. Promega makes no claims to accuracy, or ownership of these genes.

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

intraflagellar transport 88 interacts with:

The information on this page was collected from publicly accessible databases, and is periodically updated. Promega makes no claims to accuracy, or ownership of these genes.

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.

The information on this page was collected from publicly accessible databases, and is periodically updated. Promega makes no claims to accuracy, or ownership of these genes.

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