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qless - qless

Predicted to enable prenyltransferase activity. Predicted to contribute to all-trans-decaprenyl-diphosphate synthase activity. Involved in several processes, including negative regulation of apoptotic process; neuroblast development; and response to mitochondrial depolarisation. Predicted to be part of heterotetrameric polyprenyl diphosphate synthase complex. Predicted to be active in mitochondrion. Is expressed in several structures, including embryonic dorsal epidermis; embryonic esophagus; embryonic head epidermis; embryonic hypopharynx; and embryonic ventral epidermis. Human ortholog(s) of this gene implicated in primary coenzyme Q10 deficiency 2. Orthologous to human PDSS1 (decaprenyl diphosphate synthase subunit 1). [provided by Alliance of Genome Resources, Nov 2024]

Genes similar to qless

NCBI Orthologs

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Species Gene Architecture aa