IFT88 intraflagellar transport 88
Gene ID: 8100, updated on 3-Nov-2024Gene type: protein coding
Also known as: DAF19; TG737; TTC10; hTg737; D13S1056E
- See all available tests in GTR for this gene
- Go to complete Gene record for IFT88
- Go to Variation Viewer for IFT88 variants
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. [provided by RefSeq, Jul 2017]
Associated conditions
See all available tests in GTR for this gene
| Description | Tests |
|---|---|
| Cross-disorder genomewide analysis of schizophrenia, bipolar disorder, and depression. GeneReviews: Not available | |
| Genetics of coronary artery calcification among African Americans, a meta-analysis. GeneReviews: Not available | |
| GWAS of dental caries patterns in the permanent dentition. GeneReviews: Not available |
Genomic context
- Location:
- 13q12.11
- Sequence:
- Chromosome: 13; NC_000013.11 (20567157..20691444)
- Total number of exons:
- 33
Variation
| Resource | Links for this gene |
|---|---|
| ClinVar | Variants reported to ClinVar |
| dbVar | Studies and variants |
| SNP | Variation Viewer for IFT88 variants |
| Genome viewer | Explore NCBI-annotated and select non-NCBI annotated genome assemblies |
- ClinVarRelated medical variations
- dbVarLink from Gene to dbVar
- OMIMLink to related OMIM entry
- PubMed (OMIM)Gene links to PubMed derived from omim_pubmed_cited links
- RefSeq RNAsLink to Nucleotide RefSeq RNAs
- Variation ViewerRelated Variants
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