Entity Details

Primary name GPD1L
Entity type gene
Source Source Link

Details

PrimaryID23171
RefseqGeneNG_023375
SymbolGPD1L
Nameglycerol-3-phosphate dehydrogenase 1 like
Chromosome3
Location3p22.3
TaxID9606
Statuslive
SourceGenomegenomic
SourceOriginnatural
CreationDate1999-11-30
ModificationDate2021-06-22

Ontological Relatives

UniProt IDsGPD1L_HUMAN

GO terms

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GOName
GO:0002027 regulation of heart rate
GO:0005829 cytosol
GO:0005886 plasma membrane
GO:0005975 carbohydrate metabolic process
GO:0006654 phosphatidic acid biosynthetic process
GO:0006734 NADH metabolic process
GO:0009331 glycerol-3-phosphate dehydrogenase complex
GO:0010765 positive regulation of sodium ion transport
GO:0016616 oxidoreductase activity, acting on the CH-OH group of donors, NAD or NADP as acceptor
GO:0017080 sodium channel regulator activity
GO:0019674 NAD metabolic process
GO:0033137 negative regulation of peptidyl-serine phosphorylation
GO:0042803 protein homodimerization activity
GO:0044325 transmembrane transporter binding
GO:0046168 glycerol-3-phosphate catabolic process
GO:0051287 NAD binding
GO:0060373 regulation of ventricular cardiac muscle cell membrane depolarization
GO:0070062 extracellular exosome
GO:0086005 ventricular cardiac muscle cell action potential
GO:0090038 negative regulation of protein kinase C signaling
GO:2000010 positive regulation of protein localization to cell surface
GO:2000649 regulation of sodium ion transmembrane transporter activity

Diseases

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Disease IDSourceNameDescription
611777 OMIMBrugada syndrome 2 (BRGDA2)A tachyarrhythmia characterized by right bundle branch block and ST segment elevation on an electrocardiogram (ECG). It can cause the ventricles to beat so fast that the blood is prevented from circulating efficiently in the body. When this situation occurs, the individual will faint and may die in a few minutes if the heart is not reset. The gene represented in this entry may be involved in disease pathogenesis.