XB-FEAT-969901: Difference between revisions
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imported>Xenbase gene generator No edit summary |
imported>Xenbase (→gpd1l) |
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=gpd1l= | =gpd1l= | ||
This is the community wiki page for the gene ''gpd1l'' 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 ''gpd1l'' please feel free to add any information that is relevant to this gene that is not already captured elsewhere in Xenbase. | ||
=nomenclature changes= | |||
06/19/2017 | |||
Human name has changed for Entrez Gene: 23171. From glycerol-3-phosphate dehydrogenase 1-like to glycerol-3-phosphate dehydrogenase 1 like | |||
=summary from NCBI= | |||
The protein encoded by this gene catalyzes the conversion of sn-glycerol 3-phosphate to glycerone phosphate. The encoded protein is found in the cytoplasm, associated with the plasma membrane, where it binds the sodium channel, voltage-gated, type V, alpha subunit (SCN5A). Defects in this gene are a cause of Brugada syndrome type 2 (BRS2) as well as sudden infant death syndrome (SIDS). [provided by RefSeq, Jul 2010] | |||
Latest revision as of 10:01, 20 June 2017
gpd1l
This is the community wiki page for the gene gpd1l please feel free to add any information that is relevant to this gene that is not already captured elsewhere in Xenbase.
nomenclature changes
06/19/2017 Human name has changed for Entrez Gene: 23171. From glycerol-3-phosphate dehydrogenase 1-like to glycerol-3-phosphate dehydrogenase 1 like
summary from NCBI
The protein encoded by this gene catalyzes the conversion of sn-glycerol 3-phosphate to glycerone phosphate. The encoded protein is found in the cytoplasm, associated with the plasma membrane, where it binds the sodium channel, voltage-gated, type V, alpha subunit (SCN5A). Defects in this gene are a cause of Brugada syndrome type 2 (BRS2) as well as sudden infant death syndrome (SIDS). [provided by RefSeq, Jul 2010]