GPD1

GENERAL INFORMATION

? »

Gene name

GPD1

Gene description

Glycerol-3-phosphate dehydrogenase 1 (soluble)

Protein class

Disease related genes
Enzymes
Plasma proteins
Potential drug targets
Predicted intracellular proteins

Predicted localization

Intracellular

Number of transcripts

2
SHOW MORE

HUMAN PROTEIN ATLAS INFORMATION

? »

RNA tissue category

HPA:Tissue enhanced (adipose tissue)
GTEx:Tissue enhanced (adipose tissue, breast)

Protein evidence

Evidence at protein level

Protein localization

General cytoplasmic expression.

ANTIBODY RELIABILITY

? »

Data reliability
description

Antibody staining mainly not consistent with RNA expression data.

Data reliability

Uncertain based on 1 antibody.
HPA044620
SHOW MORE

RNA AND PROTEIN EXPRESSION SUMMARY

? »
RNA expression (FPKM) Protein expression (score)
Brain
Endocrine tissues
Bone marrow & immune system
Muscle tissues
Lung
Liver & gallbladder
Pancreas
Gastrointestinal tract
Kidney & urinary bladder
Male tissues
Female tissues
Adipose & soft tissue
Skin
Cerebral cortex

Lymph node

Liver

Colon

Kidney

Testis



PROTEIN EXPRESSION OVERVIEW

? »

Organ

Expression



RNA EXPRESSION OVERVIEW

? »
HPA dataset
RNA tissue category:  Tissue enhanced (adipose tissue)

Organ

Expression

GTEx dataset
RNA tissue category:  Tissue enhanced (adipose tissue, breast)

Organ

Expression



GENE INFORMATION

? »

Gene name

GPD1

Synonyms

Description

Glycerol-3-phosphate dehydrogenase 1 (soluble) (HGNC Symbol)

Entrez gene summary

This gene encodes a member of the NAD-dependent glycerol-3-phosphate dehydrogenase family. The encoded protein plays a critical role in carbohydrate and lipid metabolism by catalyzing the reversible conversion of dihydroxyacetone phosphate (DHAP) and reduced nicotine adenine dinucleotide (NADH) to glycerol-3-phosphate (G3P) and NAD+. The encoded cytosolic protein and mitochondrial glycerol-3-phosphate dehydrogenase also form a glycerol phosphate shuttle that facilitates the transfer of reducing equivalents from the cytosol to mitochondria. Mutations in this gene are a cause of transient infantile hypertriglyceridemia. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Mar 2012]

Chromosome

12

Cytoband

q13.12

Chromosome location (bp)

50103819 - 50111319

Protein evidence

Evidence at protein level (all genes)

Ensembl

ENSG00000167588 (version 78.38)

Entrez gene

2819

UniProt

P21695 (UniProt - Evidence at protein level)

neXtProt

NX_P21695

Antibodypedia

GPD1 antibodies


PROTEIN BROWSER

? »
 
 
 
ENST00000301149
 
ENST00000548814
 
 
 
 


PROTEIN INFORMATION

? »

Splice variant

Ensembl

UniProt

Protein class

Gene ontology

Length
(aa)

Molecular mass
(kDa)

Signal peptide
(predicted)

Transmembrane regions
(predicted)

GPD1-001 ENSP00000301149
ENST00000301149
P21695
Show all »
Show » Show » 349 37.6 No 0
GPD1-002 ENSP00000446768
ENST00000548814
P21695
Show all »
Show » Show » 326 35.1 No 0