Gene
prkag2b
- ID
- ZDB-GENE-070912-442
- Name
- protein kinase, AMP-activated, gamma 2 non-catalytic subunit b
- Symbol
- prkag2b Nomenclature History
- Previous Names
-
- prkag2
- si:ch211-230l11.1
- si:dkey-217f4.2
- Type
- protein_coding_gene
- Location
- Chr: 2 Mapping Details/Browsers
- Description
- Predicted to have adenyl ribonucleotide binding activity. Predicted to be involved in regulation of protein serine/threonine kinase activity. Human ortholog(s) of this gene implicated in Wolff-Parkinson-White syndrome; glycogen storage disease; hypertrophic cardiomyopathy; hypertrophic cardiomyopathy 6; and lethal congenital glycogen storage disease of heart. Orthologous to human PRKAG2 (protein kinase AMP-activated non-catalytic subunit gamma 2).
- Genome Resources
- Note
- None
- Comparative Information
-
- All Expression Data
- 1 figure from Meireles et al., 2018
- Cross-Species Comparison
- High Throughput Data
- Thisse Expression Data
- No data available
Wild Type Expression Summary
- All Phenotype Data
- No data available
- Cross-Species Comparison
- Alliance
Phenotype Summary
Mutations
Human Disease
| Disease Ontology Term | Multi-Species Data | OMIM Term | OMIM Phenotype ID |
|---|---|---|---|
| hypertrophic cardiomyopathy 6 | Alliance | Cardiomyopathy, hypertrophic 6 | 600858 |
| lethal congenital glycogen storage disease of heart | Alliance | Glycogen storage disease of heart, lethal congenital | 261740 |
| Wolff-Parkinson-White syndrome | Alliance | Wolff-Parkinson-White syndrome | 194200 |
Domain, Family, and Site Summary
Domain Details Per Protein
| Protein | Length | CBS domain | CBS domain superfamily |
|---|---|---|---|
|
UniProtKB:F1QRT4
|
533 | ||
|
UniProtKB:A0A8M2BAB8
|
532 |
| Type | Name | Annotation Method | Length (nt) | Analysis |
|---|---|---|---|---|
| mRNA |
prkag2b-201
(1)
|
Havana | 2139 nt |
Interactions and Pathways
No data available
Plasmids
No data available