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CG5921 - uncharacterized protein

Predicted to enable spectrin binding activity. Predicted to be involved in G2/M transition of mitotic cell cycle. Predicted to be located in apical part of cell. Predicted to be part of stereocilia ankle link complex. Predicted to be active in cilium; plasma membrane; and stereocilium tip. Human ortholog(s) of this gene implicated in Usher syndrome; Usher syndrome type 1; Usher syndrome type 1C; and autosomal recessive nonsyndromic deafness 18A. Orthologous to human USH1C (USH1 protein network component harmonin). [provided by Alliance of Genome Resources, Nov 2024]

Genes similar to CG5921

NCBI Orthologs

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Species Gene Architecture aa