Gene
rhag
- ID
- ZDB-GENE-030131-8229
- Name
- Rh associated glycoprotein
- Symbol
- rhag Nomenclature History
- Previous Names
-
- wu:fj61d12
- Type
- protein_coding_gene
- Location
- Chr: 20 Mapping Details/Browsers
- Description
- Predicted to have ammonium transmembrane transporter activity. Involved in ammonium transport and urea transport. Predicted to localize to integral component of plasma membrane. Human ortholog(s) of this gene implicated in Rh deficiency syndrome; hemolytic anemia; and overhydrated hereditary stomatocytosis. Is expressed in several structures, including ball; cardiovascular system; gill; hematopoietic system; and pleuroperitoneal region. Orthologous to human RHAG (Rh associated glycoprotein).
- Genome Resources
- Note
- None
- Comparative Information
-
- All Expression Data
- 13 figures from 3 publications
- Cross-Species Comparison
- High Throughput Data
- Thisse Expression Data
-
- eu1060 (11 images)
Wild Type Expression Summary
- All Phenotype Data
- 2 figures from Braun et al., 2009
- Cross-Species Comparison
- Alliance
Phenotype Summary
Mutations
Human Disease
| Disease Ontology Term | Multi-Species Data | OMIM Term | OMIM Phenotype ID |
|---|---|---|---|
| overhydrated hereditary stomatocytosis | Alliance | Overhydrated hereditary stomatocytosis | 185000 |
| Rh deficiency syndrome | Alliance | Anemia, hemolytic, Rh-null, regulator type | 268150 |
Domain, Family, and Site Summary
Domain Details Per Protein
| Protein | Length | Ammonium transporter AmtB-like domain | Ammonium/urea transporter | Blood group Rhesus C/E/D polypeptide |
|---|---|---|---|---|
|
UniProtKB:Q7T067
|
436 | |||
|
UniProtKB:A0A8M3AW33
|
413 |
Interactions and Pathways
No data available
Plasmids
No data available