XB-FEAT-5886064: Difference between revisions
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=oplah= | =oplah= | ||
This is the community wiki page for the gene ''oplah'' 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 ''oplah'' please feel free to add any information that is relevant to this gene that is not already captured elsewhere in Xenbase. | ||
= nomenclature changes= | |||
08/15/2017 | |||
Human name has changed for Entrez Gene: 26873. From 5-oxoprolinase (ATP-hydrolysing) to 5-oxoprolinase, ATP-hydrolysing | |||
=summary from NCBI= | |||
The protein encoded by this gene acts as a homodimer, using ATP hydrolysis to catalyze the conversion of 5-oxo-L-proline to L-glutamate. Defects in this gene are a cause of 5-oxoprolinase deficiency (OPLAHD). [provided by RefSeq, Jun 2012] | |||
Latest revision as of 07:31, 15 August 2017
oplah
This is the community wiki page for the gene oplah please feel free to add any information that is relevant to this gene that is not already captured elsewhere in Xenbase.
nomenclature changes
08/15/2017 Human name has changed for Entrez Gene: 26873. From 5-oxoprolinase (ATP-hydrolysing) to 5-oxoprolinase, ATP-hydrolysing
summary from NCBI
The protein encoded by this gene acts as a homodimer, using ATP hydrolysis to catalyze the conversion of 5-oxo-L-proline to L-glutamate. Defects in this gene are a cause of 5-oxoprolinase deficiency (OPLAHD). [provided by RefSeq, Jun 2012]