Rhcg - Rh family, C glycoprotein Gene

Species: Rattus norvegicus

Gene Type: protein coding
Gene ID: 293048

Summary

Enables ammonium transmembrane transporter activity. Involved in ammonium transmembrane transport. Located in apical plasma membrane; basolateral plasma membrane; and cytoplasmic vesicle. Biomarker of hypokalemia; kidney failure; and metabolic acidosis. Orthologous to human RHCG (Rh family C glycoprotein). [provided by Alliance of Genome Resources, Apr 2022]

Rhcg Products (1)

mRNA Protein Name
NM_183053.1 NP_898876.1 ammonium transporter Rh type C

Gene Ontology

  • Molecular Function
  • Biological Process
  • Cellular Component
Molecular Function GO Annotation Evidence References Source
enables ammonium channel activity IDA
IDA: Inferred from direct assay
16434569 RGD
Biological Process GO Annotation Evidence References Source
involved in ammonium transmembrane transport IDA
IDA: Inferred from direct assay
16434569 RGD
Cellular Component GO Annotation Evidence References Source
located in apical plasma membrane IDA
IDA: Inferred from direct assay
12138130 RGD
located in basal plasma membrane IDA
IDA: Inferred from direct assay
20392801 RGD
located in basolateral plasma membrane IDA
IDA: Inferred from direct assay
16144966 RGD
located in cytoplasmic vesicle IDA
IDA: Inferred from direct assay
16434569 RGD
EXP: Inferred from Experiment IDA: Inferred from direct assay IPI: Inferred from physical interaction IMP: Inferred from mutant phenotype IGI: Inferred from genetic interaction IEP: Inferred from expression pattern
Protein Preferred Names Protein Names

ammonium transporter Rh type C

  • Rh type C glycoprotein

  • Rhesus blood group-associated C glycoprotein

  • rh family type C glycoprotein

  • rhesus blood group family type C glycoprotein

Related Agents

  • Pre-clinical Phase

Pre-clinical Phase

Bioactive Molecules (1)
Cat. No. Product Name
Effect
Purity
Rare Diseases
HY-RS11940 RHCG Human Pre-designed siRNA Set A Pre-designed Set / Unkown

Orthologs Information

Species Symbol Source ID
Homo sapiens Rhcg NCBI NCBI:51458