Ammonium transporter Rh type A

Summary
UniProt ID
Q02094
Gene Symbol
RH50 RHAG
Gene ID
6005
Organism
Homo sapiens (human)
GlyGen
Q02094
PubChem
Q02094
The Human Metabolome Database
HMDBP01947
The O-GlcNAc Database
Q02094
O-GlcNAcAtlas
Q02094
Re-Glyco
Q02094
Annotation
Keyword
3D-structure Alternative splicing Ammonia transport Direct protein sequencing Disease variant Glycoprotein Hereditary hemolytic anemia Proteomics identification Reference proteome Transmembrane helix
Gene Ontology (GO)
GO Hierarchy
Sequence
MRFTFPLMAIVLEIAMIVLFGLFVEYETDQTVLEQLNITKPTDMGIFFELYPLFQDVHVMIFVGFGFLMTFLKKYGFSSVGINLLVAALGLQWGTIVQGILQSQGQKFNIGIKNMINADFSAATVLISFGAVLGKTSPTQMLIMTILEIVFFAHNEYLVSEIFKASDIGASMTIHAFGAYFGLAVAGILYRSGLRKGHENEESAYYSDLFAMIGTLFLWMFWPSFNSAIAEPGDKQCRAIVNTYFSLAACVLTAFAFSSLVEHRGKLNMVHIQNATLAGGVAVGTCADMAIHPFGSMIIGSIAGMVSVLGYKFLTPLFTTKLRIHDTCGVHNLHGLPGVVGGLAGIVAVAMGASNTSMAMQAAALGSSIGTAVVGGLMTGLILKLPLWGQPSDQNCYDDSVYWKVPKTR
Glycosylation Sites
Displaying all 3 entries
Position Description PubMed ID GlyTouCan ID Source
37
  • N-linked (GlcNAc...) asparagine
355
  • N-linked (GlcNAc...) asparagine
371
Feature
  • ProtVista GlyGen : Glycosylation Site from GlyGen
  • ProtVista UniProt : Glycosylation Site from UniProt
Disease
Displaying all 3 entries
DO ID Disease Name Source
DOID:0111562 overhydrated hereditary stomatocytosis
DOID:583 hemolytic anemia
DOID:0050641 Rh deficiency syndrome

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International Collaboration

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Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


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Last updated: April 6, 2026