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CG9391 - uncharacterized protein

Predicted to enable inositol monophosphate 1-phosphatase activity. Predicted to be involved in inositol metabolic process; inositol phosphate dephosphorylation; and signal transduction. Predicted to be located in cytoplasm. Is expressed in Bolwig organ; adult head; adult heart; organism; and spermatozoon. Human ortholog(s) of this gene implicated in autosomal recessive non-syndromic intellectual disability; bipolar disorder; intellectual disability; and schizophrenia. Orthologous to several human genes including IMPA2 (inositol monophosphatase 2). [provided by Alliance of Genome Resources, Apr 2022]

Genes similar to CG9391

NCBI Orthologs

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Species Gene Architecture aa