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CG9981 - uncharacterized protein

Predicted to enable flippase activity. Predicted to be involved in phospholipid translocation. Predicted to be located in membrane. Predicted to be part of phospholipid-translocating ATPase complex. Predicted to be active in endoplasmic reticulum and plasma membrane. Human ortholog(s) of this gene implicated in X-linked congenital hemolytic anemia; autosomal dominant nonsyndromic deafness 84; and hypomyelinating leukodystrophy 24. Orthologous to human ATP11A (ATPase phospholipid transporting 11A); ATP11B (ATPase phospholipid transporting 11B (putative)); and ATP11C (ATPase phospholipid transporting 11C). [provided by Alliance of Genome Resources, Dec 2024]

Genes similar to CG9981

NCBI Orthologs

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Species Gene Architecture aa