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MIRAGE
Ammonium transporter Rh type A
Summary
- UniProt ID
- Q02094
- Gene Symbol
-
- RH50
- RHAG
- Gene ID
- 6005
- Organism
- Homo sapiens (human)
Annotation
- Keyword
-
- 3D-structure
- Alternative splicing
- Ammonia transport
- Direct protein sequencing
- Disease variant
- Glycoprotein
- Hereditary hemolytic anemia
- Reference proteome
- Transmembrane helix
- Gene Ontology (GO)
| GO Term |
|---|
| plasma membrane |
| membrane |
| ankyrin-1 complex |
Sequence
MRFTFPLMAIVLEIAMIVLFGLFVEYETDQTVLEQLNITKPTDMGIFFELYPLFQDVHVMIFVGFGFLMTFLKKYGFSSVGINLLVAALGLQWGTIVQGILQSQGQKFNIGIKNMINADFSAATVLISFGAVLGKTSPTQMLIMTILEIVFFAHNEYLVSEIFKASDIGASMTIHAFGAYFGLAVAGILYRSGLRKGHENEESAYYSDLFAMIGTLFLWMFWPSFNSAIAEPGDKQCRAIVNTYFSLAACVLTAFAFSSLVEHRGKLNMVHIQNATLAGGVAVGTCADMAIHPFGSMIIGSIAGMVSVLGYKFLTPLFTTKLRIHDTCGVHNLHGLPGVVGGLAGIVAVAMGASNTSMAMQAAALGSSIGTAVVGGLMTGLILKLPLWGQPSDQNCYDDSVYWKVPKTR
Glycosylation Sites
G49108TO
Feature
: Glycosylation Site from GlyGen
: Glycosylation Site from UniProt
Pathway
| Pathway Name | Organism |
|---|---|
| Defective RHAG causes regulator type Rh-null hemolytic anemia (RHN) | Homo sapiens |
| Erythrocytes take up carbon dioxide and release oxygen | Homo sapiens |
| Erythrocytes take up oxygen and release carbon dioxide | Homo sapiens |
| Rhesus glycoproteins mediate ammonium transport | Homo sapiens |
Disease
| DO ID | Disease Name | Source |
|---|---|---|
| DOID:0050641 | Rh deficiency syndrome | |
| DOID:0111562 | overhydrated hereditary stomatocytosis | |
| DOID:583 | hemolytic anemia |
