PEX3
peroxisomal biogenesis factor 3
- Ensembl:
- ENSG00000034693
- UniProt:
- P56589
- OMIM:
- 603164
Cilia effects upon perturbation of PEX3
Ciliogenesis screen results (4 screens)
- Kim2016: Not Reported
- Wheway et al. 2015 (siRNA) [siRNA]: Ciliogenesis Defect (z=-3.24) 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:
- abnormal eye size; increased bone mineral density; increased bone mineral content; cornea vascularization; process of degenerative change; decreased circulating cholesterol level; abnormal eye morphology; abnormal tail morphology; decreased circulating serum albumin level; abnormal cornea morphology; increased heart weight; decreased body weight; developmental dysplasia; increased lean body mass; decreased circulating total protein level; decreased total body fat amount; decreased circulating LDL cholesterol level; abnormal vertebrae morphology; inflammation; decreased circulating HDL cholesterol level
Subcellular localization
cilia associated gene, nucleoplasm, peroxisome
Functional category
- Ciliary assembly/disassembly
Function
Knockdown of peroxisome biogenesis factor genes (PEX1 or PEX3) partially suppressed ciliogenesis(PMID: 28122914).