Gene Cluster: PYGL

Organism: Homo sapiens

phosphorylase, glycogen; liver (Hers disease, glycogen storage disease type VI)

Link to Entrez Gene

Map: 14q21-q22

GO:0000166 nucleotide binding
GO:0002060 purine binding
GO:0004645 phosphorylase activity
GO:0005524 ATP binding
GO:0005536 glucose binding
GO:0005625 soluble fraction
GO:0005634 nucleus
GO:0005730 nucleolus
GO:0005737 cytoplasm
GO:0005886 plasma membrane
GO:0005975 carbohydrate metabolic process
GO:0005977 glycogen metabolic process
GO:0008144 drug binding
GO:0008184 glycogen phosphorylase activity
GO:0016208 AMP binding
GO:0016757 transferase activity, transferring glycosyl groups
GO:0030170 pyridoxal phosphate binding
GO:0032052 bile acid binding
GO:0042593 glucose homeostasis
GO:0042803 protein homodimerization activity

Reference Sequence: NM_002863.3

2830bp CDS 114..2657

Homologous cDNA sequence in the JCRB Genebank

PYGL (5:5'UTR, C:CDS, 3:3'UTR, N:Unknown)

Human
HDG1147
Chimpanzee
PstA0012 PstA0012