1. Gene
  2. RHBG - Rh family B glycoprotein Gene

RHBG - Rh family B glycoprotein Gene

Homo sapiens

Also known as SLC42A2

Gene ID: 57127 | Gene type: protein coding

About RHBG

Cytogenetic location: 1q22 Genomic coordinates (GRCh38): 1:156,366,046-156,385,219 (from NCBI)

This gene has 9 transcripts (splice variants), 210 orthologues and 4 paralogues. Biased expression in kidney (RPKM 4.7), ovary (RPKM 3.9) and 5 other tissues.

Summary

This gene encodes one of two non-erythroid members of the Rhesus (Rh) protein family. Non-erythroid Rh protein family members are mainly expressed in the kidney and belong to the methylammonium-ammonium permease/ammonia transporters superfamily. All Rh family proteins are predicted to be transmembrane proteins with 12 membrane spanning domains and intracytoplasmic N- and C-termini. Alternative splicing of this gene results in multiple transcript variants. [provided by RefSeq, Jan 2012]

RHBG Products(6)

mRNA Protein Name
NM_001256395.2 NP_001243324.1 ammonium transporter Rh type B isoform b
NM_001256396.2 NP_001243325.1 ammonium transporter Rh type B isoform c
NM_001412175.1 NP_001399104.1 ammonium transporter Rh type B isoform d precursor
NM_001412176.1 NP_001399105.1 ammonium transporter Rh type B isoform e
NM_001412177.1 NP_001399106.1 ammonium transporter Rh type B isoform f
NM_020407.5 NP_065140.3 ammonium transporter Rh type B isoform a precursor

RHBG Protein Structure

Ammonium_transp

Ammonium_transp: Ammonium Transporter Family (26 - 417)

  • 0
  • 100
  • 200
  • 300
  • 400
  • 441 a.a.
Protein Preferred Names Protein Names

ammonium transporter Rh type B

Rhesus blood group, B glycoprotein

Related Diseases

Diseases Alias
Hemolytic Disease Of Fetus And Newborn, Rh-Induced

Rh Deficiency Syndrome

Rh Disease

HDFNRH

Rh Fetomaternal Incompatibility

Rh-Null Syndrome

Pseudohypoaldosteronism, Type I, Autosomal Recessive

Autosomal Recessive Pseudohypoaldosteronism Type 1

PHA1B

Pseudohypoaldosteronism Type 1

Pseudohypoaldosteronism, Type I

Generalized Pha1

Generalized Pseudohypoaldosteronism Type 1

Pseudohypoaldosteronism Type 1 Autosomal Recessive

Pha1

Pseudohypoaldosteronism

Pha I, Autosomal Recessive

Autosomal Recessive Pha 1

Pseudohypoaldosteronism Type 1, Recessive

Pseudohypoaldosteronism Type I

Autosomal Recessive Pha1

Pha Type 1

Pseudohypoaldosteronism 1, Autosomal Recessive

Multisystem Pseudohypoaldosteronism

Pha Type I, Autosomal Recessive

Pseudohypoaldosteronism Type I, Autosomal Recessive

Diseases Alias
Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Orthologs Information

Species Symbol Source ID
Bos taurus RHBG VGNC VGNC:55671
Rattus norvegicus RHBG RGD RGD:727813
Mus musculus RHBG MGD MGI:1927379
Felis catus RHBG VGNC VGNC:99809
Macaca mulatta RHBG VGNC VGNC:99814