Protein name: RhBG Aliases: RHBG Substrates: NH4+, NH3, methyl amine, methyl ammonium Transport type: electrogenic, no coupled ions Tissue and cellular expression: kidney, liver, skin, GI tract, sweat glands, ovaries Subcellular expression: basolateral membrane Disease: unknown Locus: 1q21.3 Sequence ID: NP_001243324.1, NM_001256395.1 NP_001243325.1, NM_001256396.1 NP_065140.3, NM_020407.4 Gene ID: 57127 Splice variants: N/D


Gene names: RHBG
Protein names and data: RHBG_HUMAN, Full=Ammonium transporter Rh type B, Full=Rhesus blood group family type B glycoprotein;Short=Rh family type B glycoprotein;Short=Rh type B glycoprotein; Length: 441 a.a., Mass: 47231 Da,
fasta formatted sequence

Function: Functions as a specific ammonium transporter
Cellular location: Basolateral cell membrane; Multi-pass membrane protein. Cytoplasmic vesicle membrane; Multi-pass membrane protein
Tissue specificity: Specifically expressed in kidney. Also detected in liver and ovary

Database cross-references

UniProt: Q9H310
NextBio: 63029
OMIM: 607079
Ensembl: ENST00000400992
GeneCard: GC01P156339
TCDB: 1.A.11.4.2
Guide to Pharmacology: SLC42A2 (1199)
SLC42 family of Rhesus glycoprotein ammonium transporters (1199)

HGNC: HGNC:14572

Genetic variants

See also Ensembl:ENST00000400992