RHBG

Protein-coding gene in the species Homo sapiens From Wikipedia, the free encyclopedia

Rh family, B glycoprotein, also known as RHBG, is an ammonia transporter protein which in humans is encoded by the RHBG gene.[5][6]

AliasesRHBG, SLC42A2, Rh family B glycoprotein (gene/pseudogene), Rh family B glycoprotein
End156,385,219 bp[1]
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RHBG
Identifiers
AliasesRHBG, SLC42A2, Rh family B glycoprotein (gene/pseudogene), Rh family B glycoprotein
External IDsOMIM: 607079; MGI: 1927379; HomoloGene: 9469; GeneCards: RHBG; OMA:RHBG - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_001256395
NM_001256396
NM_020407

NM_021375

RefSeq (protein)

NP_001243324
NP_001243325
NP_065140

NP_067350

Location (UCSC)Chr 1: 156.37 – 156.39 MbChr 3: 88.15 – 88.16 Mb
PubMed search[3][4]
Wikidata
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Function

RHBG and RHCG are non-erythroid members of the Rhesus (Rh) protein family that are mainly expressed in the kidney and belong to the methylammonium-ammonium permease/ammonia transporters superfamily. Rh family proteins are all predicted to be transmembrane proteins with 12 membrane spanning domains and intracytoplasmic N- and C-termini.[5]

References

Further reading

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