PYGL

GENERAL INFORMATION

? »

Gene name

PYGL

Gene description

Phosphorylase, glycogen, liver

Protein class

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

Predicted localization

Intracellular

Number of transcripts

3
SHOW MORE

HUMAN PROTEIN ATLAS INFORMATION

? »

RNA tissue category

HPA:Expressed in all
GTEx:Expressed in all

Protein evidence

Evidence at protein level

Protein localization

Selective cytoplasmic expression in e.g. hepatocytes, subsets of cells in bone marrow and spleen.

ANTIBODY RELIABILITY

? »

Data reliability
description

Pending RNA-based expert annotation.

Data reliability

Supportive based on 2 antibodies.
HPA000962 , HPA004119
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

Bone marrow

Lymph node

Liver

Colon

Kidney

Testis



PROTEIN EXPRESSION OVERVIEW

? »

Organ

Expression



RNA EXPRESSION OVERVIEW

? »
HPA dataset
RNA tissue category:  Expressed in all

Organ

Expression

GTEx dataset
RNA tissue category:  Expressed in all

Organ

Expression



GENE INFORMATION

? »

Gene name

PYGL

Synonyms

Description

Phosphorylase, glycogen, liver (HGNC Symbol)

Entrez gene summary

This gene encodes a homodimeric protein that catalyses the cleavage of alpha-1,4-glucosidic bonds to release glucose-1-phosphate from liver glycogen stores. This protein switches from inactive phosphorylase B to active phosphorylase A by phosphorylation of serine residue 15. Activity of this enzyme is further regulated by multiple allosteric effectors and hormonal controls. Humans have three glycogen phosphorylase genes that encode distinct isozymes that are primarily expressed in liver, brain and muscle, respectively. The liver isozyme serves the glycemic demands of the body in general while the brain and muscle isozymes supply just those tissues. In glycogen storage disease type VI, also known as Hers disease, mutations in liver glycogen phosphorylase inhibit the conversion of glycogen to glucose and results in moderate hypoglycemia, mild ketosis, growth retardation and hepatomegaly. Alternative splicing results in multiple transcript variants encoding different isoforms.[provided by RefSeq, Feb 2011]

Chromosome

14

Cytoband

q22.1

Chromosome location (bp)

50857891 - 50944736

Protein evidence

Evidence at protein level (all genes)

Ensembl

ENSG00000100504 (version 78.38)

Entrez gene

5836

UniProt

P06737 (UniProt - Evidence at protein level)

neXtProt

NX_P06737

Antibodypedia

PYGL antibodies


PROTEIN BROWSER

? »
 
 
 
ENST00000216392
 
ENST00000532462
 
ENST00000544180
 
 
 
 


PROTEIN INFORMATION

? »

Splice variant

Ensembl

UniProt

Protein class

Gene ontology

Length
(aa)

Molecular mass
(kDa)

Signal peptide
(predicted)

Transmembrane regions
(predicted)

PYGL-001 ENSP00000216392
ENST00000216392
P06737
Show all »
Show » Show » 847 97.1 No 0
PYGL-002 ENSP00000443787
ENST00000544180
P06737
Show all »
Show » Show » 813 93.1 No 0
PYGL-003 ENSP00000431657
ENST00000532462
E9PK47
Show all »
Show » Show » 819 94.1 No 0