XB-FEAT-999986: Difference between revisions
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= | =tmprss15= | ||
This is the community wiki page for the gene '' | This is the community wiki page for the gene ''tmprss15'' please feel free to add any information that is relevant to this gene that is not already captured elsewhere in Xenbase | ||
= nomenclature changes= | |||
01/22/2018 | |||
Human name has changed for Entrez Gene: 5651. From transmembrane protease, serine 15 to transmembrane serine protease 15 | |||
=Summary from NCBI= | |||
This gene encodes an enzyme that converts the pancreatic proenzyme trypsinogen to trypsin, which activates other proenzymes including chymotrypsinogen and procarboxypeptidases. The precursor protein is cleaved into two chains that form a heterodimer linked by a disulfide bond. This protein is a member of the trypsin family of peptidases. Mutations in this gene cause enterokinase deficiency, a malabsorption disorder characterized by diarrhea and failure to thrive. [provided by RefSeq, Jul 2008] | |||
Latest revision as of 09:42, 24 January 2018
tmprss15
This is the community wiki page for the gene tmprss15 please feel free to add any information that is relevant to this gene that is not already captured elsewhere in Xenbase
nomenclature changes
01/22/2018 Human name has changed for Entrez Gene: 5651. From transmembrane protease, serine 15 to transmembrane serine protease 15
Summary from NCBI
This gene encodes an enzyme that converts the pancreatic proenzyme trypsinogen to trypsin, which activates other proenzymes including chymotrypsinogen and procarboxypeptidases. The precursor protein is cleaved into two chains that form a heterodimer linked by a disulfide bond. This protein is a member of the trypsin family of peptidases. Mutations in this gene cause enterokinase deficiency, a malabsorption disorder characterized by diarrhea and failure to thrive. [provided by RefSeq, Jul 2008]