XB-FEAT-996839: Difference between revisions
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=atp13a2= | =atp13a2= | ||
This is the community wiki page for the gene ''atp13a2'' 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 ''atp13a2'' please feel free to add any information that is relevant to this gene that is not already captured elsewhere in Xenbase. | ||
=nomenclature changes= | |||
03.12.18 | |||
Human name has changed for Entrez Gene: 23400. From ATPase 13A2 to ATPase cation transporting 13A2 | |||
=Summary= | |||
This gene encodes a member of the P5 subfamily of ATPases which transports inorganic cations as well as other substrates. Mutations in this gene are associated with Kufor-Rakeb syndrome (KRS), also referred to as Parkinson disease 9. Multiple transcript variants encoding different isoforms have been found for this gene.[provided by RefSeq, Nov 2008] | |||
Latest revision as of 07:43, 14 March 2018
atp13a2
This is the community wiki page for the gene atp13a2 please feel free to add any information that is relevant to this gene that is not already captured elsewhere in Xenbase.
nomenclature changes
03.12.18 Human name has changed for Entrez Gene: 23400. From ATPase 13A2 to ATPase cation transporting 13A2
Summary
This gene encodes a member of the P5 subfamily of ATPases which transports inorganic cations as well as other substrates. Mutations in this gene are associated with Kufor-Rakeb syndrome (KRS), also referred to as Parkinson disease 9. Multiple transcript variants encoding different isoforms have been found for this gene.[provided by RefSeq, Nov 2008]