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CG17841 - uncharacterized protein

Predicted to be involved in lipid homeostasis. Predicted to be located in membrane. Predicted to be active in endoplasmic reticulum. Is expressed in several structures, including adult head; embryonic/larval oenocyte; gastric caecum; and gut section. Used to study chromosome 16p11.2 deletion syndrome, 593-kb. Human ortholog(s) of this gene implicated in cone-rod dystrophy 22. Orthologous to human TLCD3A (TLC domain containing 3A) and TLCD3B (TLC domain containing 3B). [provided by Alliance of Genome Resources, Nov 2024]

NCBI Orthologs

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Species Gene Architecture aa