Gene

pgam2

ID
ZDB-GENE-040116-6
Name
phosphoglycerate mutase 2 (muscle)
Symbol
pgam2 Nomenclature History
Previous Names
None
Type
protein_coding_gene
Location
Chr: 21 Mapping Details/Browsers
Description
Predicted to have bisphosphoglycerate mutase activity and phosphoglycerate mutase activity. Involved in myoblast fusion. Human ortholog(s) of this gene implicated in myoglobinuria. Is expressed in musculature system; pectoral fin; pericardial region; and pharyngeal arch 3-7 skeleton. Orthologous to human PGAM2 (phosphoglycerate mutase 2).
Genome Resources
Note
None
Comparative Information
Expression
All Expression Data
14 figures from Thisse et al., 2004
Cross-Species Comparison
High Throughput Data
Thisse Expression Data
Wild Type Expression Summary
Phenotype
All Phenotype Data
1 Figure from Tixier et al., 2013
Cross-Species Comparison
Alliance
Phenotype Summary
Mutations
Mutants
Sequence Targeting Reagents
Human Disease
Associated With pgam2 Human Ortholog
Disease Ontology Term Multi-Species Data OMIM Term OMIM Phenotype ID
Glycogen storage disease X 261670
Associated With pgam2 Via Experimental Models
No data available
Gene Ontology
Protein Domains
Domain, Family, and Site Summary
Type InterPro ID Name
Active_site IPR001345 Phosphoglycerate/bisphosphoglycerate mutase, active site
Family IPR005952 Phosphoglycerate mutase 1
Family IPR013078 Histidine phosphatase superfamily, clade-1
Homologous_superfamily IPR029033 Histidine phosphatase superfamily
Domain Details Per Protein
Protein Length Histidine phosphatase superfamily Histidine phosphatase superfamily, clade-1 Phosphoglycerate/bisphosphoglycerate mutase, active site Phosphoglycerate mutase 1
UniProtKB:Q7T3G4 255
Transcripts
Genome Browsers
Interactions and Pathways
No data available
Antibodies
No data available
Plasmids
No data available
Constructs
Marker Relationships
Sequences
Orthology
Comparative Orthology
Alliance
Gene Tree
Ensembl
Citations