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. Is expressed in several structures, including ball; cardiovascular system; gill; hematopoietic system; and pleuroperitoneal region. Human ortholog(s) of this gene implicated in Rh deficiency syndrome; hemolytic anemia; and overhydrated hereditary stomatocytosis. 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