Identity
HGNC
LOCATION
13q12.11
LOCUSID
ALIAS
D13S1056E,DAF19,TG737,TTC10,hTg737
FUSION GENES
Non-annotated gene. Preliminary data : if you are an author who wish to write a full paper/card on this gene, contribute in submission tool
Other Information
Locus ID:
NCBI: 8100
MIM: 600595
HGNC: 20606
Ensembl: ENSG00000032742
Variants:
dbSNP: 8100
ClinVar: 8100
TCGA: ENSG00000032742
COSMIC: IFT88
RNA/Proteins
Expression (GTEx)
Pathways
References
| Pubmed ID | Year | Title | Citations |
|---|---|---|---|
| 36084949 | 2022 | Multifaceted investigation underlies diverse mechanisms contributing to the downregulation of Hedgehog pathway-associated genes INTU and IFT88 in lung adenocarcinoma and uterine corpus endometrial carcinoma. | 2 |
| 36084949 | 2022 | Multifaceted investigation underlies diverse mechanisms contributing to the downregulation of Hedgehog pathway-associated genes INTU and IFT88 in lung adenocarcinoma and uterine corpus endometrial carcinoma. | 2 |
| 31891309 | 2020 | Ciliary Localization of the Intraflagellar Transport Protein IFT88 Is Disrupted in Cystic Fibrosis. | 4 |
| 31891309 | 2020 | Ciliary Localization of the Intraflagellar Transport Protein IFT88 Is Disrupted in Cystic Fibrosis. | 4 |
| 30953423 | 2019 | Association of IFT88 gene variants with nonsyndromic cleft lip with or without cleft palate. | 2 |
| 31312011 | 2019 | IFT88 controls NuMA enrichment at k-fibers minus-ends to facilitate their re-anchoring into mitotic spindles. | 3 |
| 30953423 | 2019 | Association of IFT88 gene variants with nonsyndromic cleft lip with or without cleft palate. | 2 |
| 31312011 | 2019 | IFT88 controls NuMA enrichment at k-fibers minus-ends to facilitate their re-anchoring into mitotic spindles. | 3 |
| 29743590 | 2018 | Loss-of-function of IFT88 determines metabolic phenotypes in thyroid cancer. | 19 |
| 29866362 | 2018 | Super-Resolution Imaging Reveals TCTN2 Depletion-Induced IFT88 Lumen Leakage and Ciliary Weakening. | 8 |
| 29978320 | 2018 | IFT88 mutations identified in individuals with non-syndromic recessive retinal degeneration result in abnormal ciliogenesis. | 11 |
| 29743590 | 2018 | Loss-of-function of IFT88 determines metabolic phenotypes in thyroid cancer. | 19 |
| 29866362 | 2018 | Super-Resolution Imaging Reveals TCTN2 Depletion-Induced IFT88 Lumen Leakage and Ciliary Weakening. | 8 |
| 29978320 | 2018 | IFT88 mutations identified in individuals with non-syndromic recessive retinal degeneration result in abnormal ciliogenesis. | 11 |
| 28489570 | 2017 | Transcriptome profiling identifies a recurrent CRYL1-IFT88 chimeric transcript in hepatocellular carcinoma. | 8 |
Citation
Dessen P
IFT88 (intraflagellar transport 88)
Atlas Genet Cytogenet Oncol Haematol. 2003-02-01
Online version: http://atlasgeneticsoncology.org/gene/42722/ift88-(intraflagellar-transport-88)
