XB-FEAT-29082542: Difference between revisions

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(Created page with "=''cyp2k1.3''= This is the community wiki page for ''cyp2k1.3''. Feel free to record here any information relevant to this gene that is not captured elsewhere on Xenbase. =nomenclature changes= 12March2024 'Xenopus'' gene name changed from ''LOC100494424'' and ''XB5870673'' to ''cyp2k1.7'' following a assessment of synteny for this region of chr5/5L/5S, which contains are cluster of 30 cytochrome p450 genes. ''Xenopus'' nomenclature rules were applied for duplicated ge...")
 
 
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12March2024
12March2024
'Xenopus'' gene name changed from ''LOC100494424'' and ''XB5870673'' to ''cyp2k1.7'' following a assessment of synteny for this region of chr5/5L/5S, which contains are cluster of 30 cytochrome p450 genes. ''Xenopus'' nomenclature rules were applied for duplicated genes, and new gene symbols were based on the existing given NCBI gene/protein characterization in the v10 genome assemblies (ie no additional phylogenetic analysis or protein domain analysis was done to check that these designations held to be true).
'Xenopus'' gene name changed from ''LOC100495056'' to ''cyp2k1.3'' following a assessment of synteny for this region of chr5/5L/5S, which contains are cluster of 30 'cytochrome p450' genes. ''Xenopus'' nomenclature rules were applied for duplicated genes, and new gene symbols were based on the existing given NCBI gene/protein characterization in the v10 genome assemblies (ie no additional phylogenetic analysis or protein domain analysis was done to check that these designations held to be true).

Latest revision as of 07:11, 14 March 2024

cyp2k1.3

This is the community wiki page for cyp2k1.3. Feel free to record here any information relevant to this gene that is not captured elsewhere on Xenbase.

nomenclature changes

12March2024 'Xenopus gene name changed from LOC100495056 to cyp2k1.3 following a assessment of synteny for this region of chr5/5L/5S, which contains are cluster of 30 'cytochrome p450' genes. Xenopus nomenclature rules were applied for duplicated genes, and new gene symbols were based on the existing given NCBI gene/protein characterization in the v10 genome assemblies (ie no additional phylogenetic analysis or protein domain analysis was done to check that these designations held to be true).