Gene: IFT88

Alternate names for this Gene: D13S1056E|DAF19|TG737|TTC10|hTg737

Gene Summary: 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.

Gene is located in Chromosome: 13

Location in Chromosome : 13q12.11

Description of this Gene: intraflagellar transport 88

Type of Gene: protein-coding

rs73165468 in IFT88 gene and Drug-induced neutropenia PMID 28762467 2018 Sulfasalazine-Induced Agranulocytosis Is Associated With the Human Leukocyte Antigen Locus.