GPR22
G protein-coupled receptor 22
Tier: Gold Standard Ciliary Genes
- Ensembl:
- ENSG00000283812
- UniProt:
- Q99680
- OMIM:
- 601910
Cilia effects upon perturbation of GPR22
- Loss-of-function effect:
- Abnormal / altered cilia
- Overexpression effect:
- Abnormal / altered
Ciliogenesis screen results (4 screens)
- Kim2016: Not Reported
- Wheway et al. 2015 (siRNA) [siRNA]: Ciliogenesis Defect (z=-5.97) 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 gait, decreased total body fat amount, decreased erythrocyte cell number, decreased hemoglobin content, hyperactivity, increased lean body mass, decreased hematocrit, increased circulating potassium level, decreased circulating serum albumin level, increased circulating phosphate level
Subcellular localization
cilia
References: PMID:25335082
Functional category
- Ciliary assembly/disassembly
- Signaling (Hedgehog, GPCRs, ion channels)
- Cilia length regulation
Function
Regulation of Left-Right asymmetry through the Kupffer’s vesicle (KV) and mantains cilia length and structure in KV. Both knockdown and overexpression of gpr22 in the Kupffer’s vesicle result in abnormal cilia length and ultrastructure, leading to defects in left–right axis formation. (25335082)