XB-FEAT-1010833: Difference between revisions
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=usp9x= | =usp9x= | ||
This is the community wiki page for the gene ''usp9x'' please feel free to add any information that is relevant to this gene that is not already captured elsewhere in Xenbase | This is the community wiki page for the gene ''usp9x'' please feel free to add any information that is relevant to this gene that is not already captured elsewhere in Xenbase | ||
=nomenclature changes= | |||
05.08.2018 | |||
Human name has changed for Entrez Gene: 8239. From ubiquitin specific peptidase 9, X-linked to ubiquitin specific peptidase 9 X-linked | |||
=summary from NCBI= | |||
This gene is a member of the peptidase C19 family and encodes a protein that is similar to ubiquitin-specific proteases. Though this gene is located on the X chromosome, it escapes X-inactivation. Mutations in this gene have been associated with Turner syndrome. Alternate transcriptional splice variants, encoding different isoforms, have been characterized. [provided by RefSeq, Jul 2008] | |||
Latest revision as of 06:38, 8 May 2018
usp9x
This is the community wiki page for the gene usp9x please feel free to add any information that is relevant to this gene that is not already captured elsewhere in Xenbase
nomenclature changes
05.08.2018 Human name has changed for Entrez Gene: 8239. From ubiquitin specific peptidase 9, X-linked to ubiquitin specific peptidase 9 X-linked
summary from NCBI
This gene is a member of the peptidase C19 family and encodes a protein that is similar to ubiquitin-specific proteases. Though this gene is located on the X chromosome, it escapes X-inactivation. Mutations in this gene have been associated with Turner syndrome. Alternate transcriptional splice variants, encoding different isoforms, have been characterized. [provided by RefSeq, Jul 2008]