RHCG
Rh family C glycoprotein
Summary
Enables several functions, including ammonium channel activity; ankyrin binding activity; and carbon dioxide transmembrane transporter activity. Involved in ammonium transmembrane transport; intracellular monoatomic ion homeostasis; and transepithelial ammonium transport. Located in apical plasma membrane and basolateral plasma membrane. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants35 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs139876872 | 15:90,015,985 | G/A | — | uncertain significance |
| rs563452263 | 15:90,016,051 | G/A | — | uncertain significance |
| rs1416970793 | 15:90,016,080 | G/C | — | likely benign |
| rs200584986 | 15:90,020,032 | C/A | — | uncertain significance |
| rs2505205812 | 15:90,020,042 | G/A | — | uncertain significance |
| rs761884034 | 15:90,020,367 | T/C | — | uncertain significance |
| rs777583931 | 15:90,020,403 | C/T | — | likely benign |
| rs770596441 | 15:90,020,412 | C/T | — | uncertain significance |
| rs1596402766 | 15:90,020,821 | G/A | — | uncertain significance |
| rs186987731 | 15:90,020,848 | A/C | — | uncertain significance |
| rs747071051 | 15:90,020,869 | G/A | — | uncertain significance |
| rs199512977 | 15:90,021,097 | T/C | — | likely benign |
| rs139070731 | 15:90,021,103 | C/T | — | uncertain significance |
| rs753219521 | 15:90,021,115 | C/T | — | uncertain significance |
| rs923645329 | 15:90,021,156 | G/A | — | uncertain significance |
| rs139841033 | 15:90,021,166 | C/A | — | uncertain significance |
| rs774803760 | 15:90,021,184 | G/A | — | uncertain significance |
| rs768044049 | 15:90,022,609 | C/T | — | uncertain significance |
| rs2505212783 | 15:90,022,652 | C/G | — | uncertain significance |
| rs2505215197 | 15:90,023,555 | T/G | — | uncertain significance |
| rs201496699 | 15:90,023,557 | C/T | — | uncertain significance |
| rs779033141 | 15:90,023,579 | C/T | — | uncertain significance |
| rs184276709 | 15:90,026,333 | C/T | — | uncertain significance |
| rs573034872 | 15:90,027,076 | G/A | — | — |
| rs1471626663 | 15:90,030,055 | G/A | — | uncertain significance |
| rs773304352 | 15:90,030,127 | T/C | — | uncertain significance |
| rs1961383476 | 15:90,030,142 | T/A | — | uncertain significance |
| rs1258451860 | 15:90,030,181 | A/G | — | uncertain significance |
| rs1961385842 | 15:90,030,210 | T/C | — | uncertain significance |
| rs1961566358 | 15:90,039,603 | T/C | — | uncertain significance |
| rs2505245324 | 15:90,039,634 | T/C | — | uncertain significance |
| rs2505245403 | 15:90,039,655 | A/G | — | uncertain significance |
| rs181242584 | 15:90,039,687 | A/G | — | uncertain significance |
| rs1961571350 | 15:90,039,739 | G/A | — | uncertain significance |
| rs776088646 | 15:90,039,762 | G/A | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.