IDE
insulin degrading enzyme
Tier: Cilia-Associated Genes
- Ensembl:
- ENSG00000119912
- UniProt:
- P14735
- OMIM:
- 146680
Cilia effects upon perturbation of IDE
- Cilia number / % ciliated:
- Decreased cilia number
- Loss-of-function effect:
- Shorter cilia
Ciliogenesis screen results (3 screens)
- Wheway et al. 2015 (siRNA) [siRNA]: Ciliogenesis Defect (z=-6.43) PMID:26167766
- Breslow et al. 2018 (CRISPR) [CRISPR]: No Significant Effect PMID:29459680
- Roosing et al. 2015 (siRNA) [siRNA]: No effect PMID:26595381
Phenotypes
- Mouse phenotype:
- increased circulating amylase level, decreased total body fat amount, process of degenerative change, abnormal incisor morphology, developmental and structural abnormality, abnormal maxilla morphology, increased lean body mass, abnormal hair texture
Subcellular localization
cytosol, mitochondria, nucleus, peroxisome
References: PMID:35652923
Functional category
- Ciliary assembly/disassembly
- Viral interactions
- Signaling (Hedgehog, GPCRs, ion channels)
Function
IDE deficiency triggers impairments in cilia formation, inducing alpha cell hyperplasia and possibly also contributing to dysregulated glucagon secretion and hyperglucago emia ( 35652923). IDE deficiency triggers impairments in cilia formation, inducing alpha cell hyperplasia (35652923) We found a decreased number of cilia in siRNA-Ide cells compared to its control. In addition, we observed that the average length of primary cilia was significantly shorter in siRNA-Ide αTC1.9 cells compared to control cells, indicating that the knockdown of Ide affects correct ciliogenesis.