G6PD

GENERAL INFORMATION

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Gene name

G6PD

Gene description

Glucose-6-phosphate dehydrogenase

Protein class

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

Predicted localization

Intracellular

Number of transcripts

7
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HUMAN PROTEIN ATLAS INFORMATION

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RNA tissue category

HPA:Expressed in all
GTEx:Expressed in all

Protein evidence

Evidence at protein level

Protein localization

General cytoplasmic expression most abundant in seminiferus duct cells, spleen and bone marrow.

ANTIBODY RELIABILITY

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Data reliability
description

Pending RNA-based expert annotation.

Data reliability

Supportive based on 2 antibodies.
HPA000247 , HPA000834
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RNA AND PROTEIN EXPRESSION SUMMARY

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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

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Organ

Expression



RNA EXPRESSION OVERVIEW

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HPA dataset
RNA tissue category:  Expressed in all

Organ

Expression

GTEx dataset
RNA tissue category:  Expressed in all

Organ

Expression



GENE INFORMATION

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Gene name

G6PD (HGNC Symbol)

Synonyms

G6PD1

Description

Glucose-6-phosphate dehydrogenase (HGNC Symbol)

Entrez gene summary

This gene encodes glucose-6-phosphate dehydrogenase. This protein is a cytosolic enzyme encoded by a housekeeping X-linked gene whose main function is to produce NADPH, a key electron donor in the defense against oxidizing agents and in reductive biosynthetic reactions. G6PD is remarkable for its genetic diversity. Many variants of G6PD, mostly produced from missense mutations, have been described with wide ranging levels of enzyme activity and associated clinical symptoms. G6PD deficiency may cause neonatal jaundice, acute hemolysis, or severe chronic non-spherocytic hemolytic anemia. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]

Chromosome

X

Cytoband

q28

Chromosome location (bp)

154531391 - 154547572

Protein evidence

Evidence at protein level (all genes)

Ensembl

ENSG00000160211 (version 78.38)

Entrez gene

2539

UniProt

P11413 (UniProt - Evidence at protein level)

neXtProt

NX_P11413

Antibodypedia

G6PD antibodies


PROTEIN BROWSER

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ENST00000369620
 
ENST00000393562
 
ENST00000393564
 
ENST00000433845
 
ENST00000439227
 
ENST00000440967
 
ENST00000621232
 
 
 
 


PROTEIN INFORMATION

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Splice variant

Ensembl

UniProt

Protein class

Gene ontology

Length
(aa)

Molecular mass
(kDa)

Signal peptide
(predicted)

Transmembrane regions
(predicted)

G6PD-001 ENSP00000377192
ENST00000393562
P11413
Show all »
Show » Show » 545 62.5 No 0
G6PD-002 ENSP00000395599
ENST00000439227
E7EUI8
Show all »
Show » Show » 339 38.5 No 0
G6PD-005 ENSP00000394690
ENST00000433845
E9PD92
Show all »
Show » Show » 256 29.5 No 0
G6PD-006 ENSP00000377194
ENST00000393564
P11413
Show all »
Show » Show » 515 59.3 No 0
G6PD-007 ENSP00000400648
ENST00000440967
E7EM57
Show all »
Show » Show » 320 36.5 No 0
G6PD-010 ENSP00000358633
ENST00000369620
P11413
Show all »
Show » Show » 561 63.8 No 0
G6PD-201 ENSP00000483686
ENST00000621232
P11413
Show all »
Show » Show » 515 59.3 No 0