XB-FEAT-991705: Difference between revisions
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= | = ''saxo6'' = | ||
This is the community wiki page for the gene '' | This is the community wiki page for the gene ''saxo6'' please feel free to add any information that is relevant to this gene that is not already captured elsewhere in Xenbase. | ||
=nomenclature changes= | |||
22JUN2015 | |||
Human name has changed for Entrez Gene: 56890. From Mdm1 nuclear protein homolog (mouse) to Mdm1 nuclear protein | |||
29APR2026 | |||
''Xenopus'' gene names changed from ''mdm1, Mdm1 nuclear protein'' to ''saxo6, stabilizer of axonemal microtubules 6'' following human name changes. | |||
=summary from NCBI for human SAXO6= | |||
This gene encodes a microtubule-binding nuclear protein that localizes to the centrioles of dividing cells and differentiating multiciliated cells and negatively regulates centriole duplication. The encoded protein is closely associated with the centriole barrel, and resides in the centriole lumen. Naturally-occurring mutations in the orthologous mouse gene are associated with age-related retinal degeneration. [provided by RefSeq, Feb 2019] | |||
Latest revision as of 20:13, 29 April 2026
saxo6
This is the community wiki page for the gene saxo6 please feel free to add any information that is relevant to this gene that is not already captured elsewhere in Xenbase.
nomenclature changes
22JUN2015 Human name has changed for Entrez Gene: 56890. From Mdm1 nuclear protein homolog (mouse) to Mdm1 nuclear protein
29APR2026
Xenopus gene names changed from mdm1, Mdm1 nuclear protein to saxo6, stabilizer of axonemal microtubules 6 following human name changes.
summary from NCBI for human SAXO6
This gene encodes a microtubule-binding nuclear protein that localizes to the centrioles of dividing cells and differentiating multiciliated cells and negatively regulates centriole duplication. The encoded protein is closely associated with the centriole barrel, and resides in the centriole lumen. Naturally-occurring mutations in the orthologous mouse gene are associated with age-related retinal degeneration. [provided by RefSeq, Feb 2019]