XB-FEAT-921488: Difference between revisions
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=ptprq= | =ptprq= | ||
This is the community wiki page for the gene ''ptprq'' 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 ''ptprq'' please feel free to add any information that is relevant to this gene that is not already captured elsewhere in Xenbase | ||
=nomenclature changes= | |||
01/12/2016 | |||
Human name has changed for Entrez Gene: 374462. From protein tyrosine phosphatase, receptor type, Q to protein tyrosine phosphatase, receptor type Q | |||
05.13.19 | |||
Human name has changed for Entrez Gene: 374462. From protein tyrosine phosphatase, receptor type Q to protein tyrosine phosphatase receptor type Q | |||
=Summary from NCBI, human PTPRQ= | |||
This locus encodes a member of the type III receptor-like protein-tyrosine phosphatase family. The encoded protein catalyzes the dephosphorylation of phosphotyrosine and phosphatidylinositol and plays roles in cellular proliferation and differentiation. Mutations at this locus have been linked to autosomal recessive deafness. [provided by RefSeq, Mar 2014] | |||
Latest revision as of 07:29, 15 May 2019
ptprq
This is the community wiki page for the gene ptprq please feel free to add any information that is relevant to this gene that is not already captured elsewhere in Xenbase
nomenclature changes
01/12/2016
Human name has changed for Entrez Gene: 374462. From protein tyrosine phosphatase, receptor type, Q to protein tyrosine phosphatase, receptor type Q
05.13.19
Human name has changed for Entrez Gene: 374462. From protein tyrosine phosphatase, receptor type Q to protein tyrosine phosphatase receptor type Q
Summary from NCBI, human PTPRQ
This locus encodes a member of the type III receptor-like protein-tyrosine phosphatase family. The encoded protein catalyzes the dephosphorylation of phosphotyrosine and phosphatidylinositol and plays roles in cellular proliferation and differentiation. Mutations at this locus have been linked to autosomal recessive deafness. [provided by RefSeq, Mar 2014]