XB-FEAT-969901

From XenWiki
Revision as of 09:01, 20 June 2017 by imported>Xenbase (→‎gpd1l)
(diff) ← Older revision | Latest revision (diff) | Newer revision → (diff)
Jump to navigation Jump to search

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]