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drpr - draper

Enables phosphatidylserine binding activity. Involved in several processes, including autophagic cell death; cell competition in a multicellular organism; and engulfment of apoptotic cell. Located in several cellular components, including axon; plasma membrane; and postsynapse. Is expressed in several structures, including CNS glial cell; adult fat body; adult head; brain; and synaptic neuropil domain. Used to study myopathy and neurodegenerative disease. Human ortholog(s) of this gene implicated in congenital myopathy 10B and early-onset myopathy-areflexia-respiratory distress-dysphagia syndrome. Orthologous to several human genes including MEGF10 (multiple EGF like domains 10) and MEGF11 (multiple EGF like domains 11). [provided by Alliance of Genome Resources, Nov 2024]

Genes similar to drpr

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Species Gene Architecture aa