Gene
vma21
- ID
- ZDB-GENE-081104-272
- Name
- vacuolar ATPase assembly factor VMA21
- Symbol
- vma21 Nomenclature History
- Previous Names
-
- si:ch73-26o5.1
- Type
- protein_coding_gene
- Location
- Chr: 5 Mapping Details/Browsers
- Description
- Predicted to be involved in vacuolar proton-transporting V-type ATPase complex assembly. Predicted to localize to bounding membrane of organelle; endoplasmic reticulum; and integral component of membrane. Human ortholog(s) of this gene implicated in X-linked myopathy with excessive autophagy. Orthologous to human VMA21 (vacuolar ATPase assembly factor VMA21).
- Genome Resources
- Note
- None
- Comparative Information
-
- All Expression Data
- No data available
- 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 |
|---|---|---|---|
| X-linked myopathy with excessive autophagy | Alliance | Myopathy, X-linked, with excessive autophagy | 310440 |
Domain, Family, and Site Summary
| Type | InterPro ID | Name |
|---|---|---|
| Family | IPR019013 | Vacuolar ATPase assembly integral membrane protein Vma21 |
Domain Details Per Protein
| Protein | Length | Vacuolar ATPase assembly integral membrane protein Vma21 |
|---|---|---|
|
UniProtKB:B8JLV7
|
Interactions and Pathways
No data available
Plasmids
No data available
- Comparative Orthology
- Alliance