Intraflagellar transport protein 88 homolog is a protein that is encoded by the IFT88 gene. This gene encodes a member of the tetratrico peptide repeat (TPR)...
(cranioectodermal dysplasia) 218330 IFT122 Short rib–polydactyly syndrome 613091 DYNC2H1 ? ? IFT88 Novel form of congenital anosmia, reported in 2012...
chemicals, and an adenovirus was used to implant a working version of the IFT88 gene into defective cells in the nose, which restored the cilia and allowed...
still present in all wolves and dogs today. The variant affects a gene, IFT88, which is involved in the development of bones in the skull and jaw. It...
(January 2020). "The association of microcephaly protein WDR62 with CPAP/IFT88 is required for cilia formation and neocortical development". Human Molecular...
required for chondrocyte mechanotransduction. Chondrocytes derived from IFT88 mutant mice did not express primary cilia and did not show the characteristic...
centrosome localization of CENPJ and the Intraflagellar transport protein 88 (IFT88), which are required for tubulin requitment to centrosome and transport...
(January 2020). "The association of microcephaly protein WDR62 with CPAP/IFT88 is required for cilia formation and neocortical development". Human Molecular...
this gene. BAT2 has been shown to interact with: C1QBP, EIF3S6, HNRNPA1, IFT88, IMMT, and UBAP2L. ENSG00000206427, ENSG00000231825, ENSG00000231370, ENSG00000226618...
develops is critical. The researchers discovered that a deletion of the IFT88 gene, which is a key protein for the IFT-B complex, also showed an increased...
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