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CG11109 - uncharacterized protein

Predicted to enable tRNA (cytidine-5-)-methyltransferase activity. Predicted to be involved in RNA methylation and tRNA modification. Is expressed in organism and spermatozoon. Used to study syndromic intellectual disability. Human ortholog(s) of this gene implicated in autosomal recessive intellectual developmental disorder 82. Orthologous to human NSUN6 (NOP2/Sun RNA methyltransferase 6). [provided by Alliance of Genome Resources, Nov 2024]

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Species Gene Architecture aa