XB-FEAT-1012246: Difference between revisions
Jump to navigation
Jump to search
imported>Xenbase gene generator No edit summary |
|||
Line 1: | Line 1: | ||
=phex= | =''phex''= | ||
This is the community wiki page for the gene ''phex'' 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 ''phex'' please feel free to add any information that is relevant to this gene that is not already captured elsewhere in Xenbase | ||
=nomenclature changes= | |||
17JULY2022 | |||
Human name has changed for Entrez Gene: 5251. From phosphate regulating endopeptidase homolog X-linked to phosphate regulating endopeptidase X-linked | |||
=summary for human PHEX from NCBI= | |||
The protein encoded by this gene is a transmembrane endopeptidase that belongs to the type II integral membrane zinc-dependent endopeptidase family. The protein is thought to be involved in bone and dentin mineralization and renal phosphate reabsorption. Mutations in this gene cause ''X-linked hypophosphatemic rickets''. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Sep 2013] |
Latest revision as of 14:50, 3 August 2022
phex
This is the community wiki page for the gene phex please feel free to add any information that is relevant to this gene that is not already captured elsewhere in Xenbase
nomenclature changes
17JULY2022
Human name has changed for Entrez Gene: 5251. From phosphate regulating endopeptidase homolog X-linked to phosphate regulating endopeptidase X-linked
summary for human PHEX from NCBI
The protein encoded by this gene is a transmembrane endopeptidase that belongs to the type II integral membrane zinc-dependent endopeptidase family. The protein is thought to be involved in bone and dentin mineralization and renal phosphate reabsorption. Mutations in this gene cause X-linked hypophosphatemic rickets. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Sep 2013]