MEGF10
multiple EGF like domains 10
- Ensembl:
- ENSG00000145794
- UniProt:
- Q96KG7
- OMIM:
- 612453
- Synonyms:
- KIAA1780, SR-F3, EMARDD, CMYO10A, CMYO10B
Cilia effects upon perturbation of MEGF10
- Cilia number / % ciliated:
- Unknown
- Loss-of-function effect:
- Unknown
- Overexpression effect:
- Unknown
Ciliogenesis screen results (1 screen)
- Elliott et al. 2025 (CRISPRa) [CRISPRa]: Disassembly Trigger (casTLE Effect=-2.20) PMID:41160700
Phenotypes
- Mouse phenotype:
- abnormal retina mosaic patterning of starburst amacrine cells; muscle satellite cell defects
Subcellular localization
cilia, plasma membrane
Functional category
- Phagocytic receptor
- Cell-cell adhesion
- Cilium-derived extracellular vesicles
Function
Single-pass transmembrane phagocytic receptor with N-terminal EMI domain followed by 17 atypical EGF-like extracellular repeats and cytoplasmic NPxY/YxxL motifs. Mammalian ortholog of C. elegans CED-1 and Drosophila Draper. Established mammalian functions: engulfing-cell receptor for apoptotic corpses (binding C1q and phosphatidylserine eat-me signal); regulator of skeletal muscle satellite cell proliferation/differentiation via Notch signaling; mediator of mosaic spacing of starburst amacrine cells in retina via homotypic neuron repulsion; uptake of amyloid-beta peptides in brain. C. elegans CED-1 localizes to dendrites and primary cilia of male tail RnB sensory neurons, where loss of ced-1 reduces ciliary abundance of PKD-2 and CLHM-1 ion channels and reduces extracellular vesicle shedding from the cilium distal tip in response to mating partners (Ke and Tanis 2025, bioRxiv 10.1101/2025.09.15.676301). Mammalian ciliary role not yet directly demonstrated; preprint authors speculate conserved function.
Model organism evidence
C. elegans CED-1::mNG localizes to dendrites and the ciliary region of B-type ray sensory neurons (Ke & Tanis 2025).
Loss of ced-1 reduces ciliary abundance of PKD-2 and CLHM-1 ion channels and reduces extracellular vesicle shedding from the cilium distal tip in response to mating partners.
PMIDs: PMC12670632
Megf10 knockout: abnormal retina mosaic patterning of starburst amacrine cells; muscle satellite cell defects. Direct ciliary phenotype not yet reported in mouse.