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Genes search result for Homo sapiens
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2 records found for search term Coq5
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RGD IDSymbolNameDescriptionChrStartStopSpeciesAnnotationsMatchType
1604266COQ5coenzyme Q5, methyltransferaseEnables 2-methoxy-6-polyprenyl-1,4-benzoquinol methyltransferase activity. Involved in methylation and ubiquinone biosynthetic process. Located in mitochondrial inner membrane and mitochondrial matrix. Part of ubiquinone biosynthesis complex. Implicated in primary coenzyme Q10 deficiency 9. [provide12120503279120529158Human127symbol , old_gene_name , COSMIC , Human Proteome Mapgene, protein-coding, VALIDATED [RefSeq]
1352777METTL27methyltransferase like 27This gene encodes a protein belonging to ubiE/COQ5 methyltransferase family. The gene is deleted in Williams syndrome, a multisystem developmental disorder caused by the deletion of contiguous genes at 7q11.22-q11.23. [provided by RefSeq, Jul 2008]77383459073842516Human246descriptiongene, protein-coding, REVIEWED [RefSeq]