Gene
prmt7
- ID
- ZDB-GENE-040426-1560
- Name
- protein arginine methyltransferase 7
- Symbol
- prmt7 Nomenclature History
- Previous Names
-
- zgc:66172
- Type
- protein_coding_gene
- Location
- Chr: 25 Mapping Details/Browsers
- Description
- Predicted to have histone methyltransferase activity (H4-R3 specific); protein-arginine omega-N monomethyltransferase activity; and protein-arginine omega-N symmetric methyltransferase activity. Predicted to be involved in macromolecule methylation; regulation of gene expression by genetic imprinting; and spliceosomal snRNP assembly. Predicted to localize to cytosol and nucleus. Is expressed in adaxial cell; brain; eye; otic vesicle; and somite. Orthologous to human PRMT7 (protein arginine methyltransferase 7).
- Genome Resources
- Note
- None
- Comparative Information
-
- All Expression Data
- 4 figures from 3 publications
- Cross-Species Comparison
- High Throughput Data
- Thisse Expression Data
-
- MGC:66172 (1 image)
Wild Type Expression Summary
Phenotype Summary
Mutations
Human Disease
| Disease Ontology Term | Multi-Species Data | OMIM Term | OMIM Phenotype ID |
|---|---|---|---|
| Short stature, brachydactyly, intellectual developmental disability, and seizures | 617157 |
Domain, Family, and Site Summary
Domain Details Per Protein
| Protein | Length | Protein arginine N-methyltransferase | Protein arginine N-methyltransferase PRMT7 | S-adenosyl-L-methionine-dependent methyltransferase superfamily |
|---|---|---|---|---|
|
UniProtKB:A2AV36
|
683 | |||
|
UniProtKB:A0A8M6YVX1
|
550 |
Interactions and Pathways
No data available
Plasmids
No data available