IL20RA
interleukin 20 receptor subunit alpha
Summary
This gene encodes a member of the type II cytokine receptor family. The encoded protein is a subunit of the receptor for interleukin 20, a cytokine that may be involved in epidermal function. The interleukin 20 receptor is a heterodimeric complex consisting of the encoded protein and interleukin 20 receptor beta. This gene and interleukin 20 receptor beta are highly expressed in skin, and are upregulated in psoriasis. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2013]
Known Variants34 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs186439336 | 6:137,322,720 | C/G | — | uncertain significance |
| rs755010486 | 6:137,322,729 | T/C | — | uncertain significance |
| rs1015688435 | 6:137,322,799 | T/C | — | uncertain significance |
| rs200592228 | 6:137,322,820 | C/T | — | uncertain significance |
| rs778260609 | 6:137,322,859 | C/T | — | uncertain significance |
| rs147020946 | 6:137,323,002 | G/C | — | uncertain significance |
| rs143448674 | 6:137,323,017 | T/C | — | uncertain significance |
| rs377051637 | 6:137,323,068 | G/A | — | uncertain significance |
| rs138424318 | 6:137,323,071 | C/T | — | uncertain significance |
| rs1775074776 | 6:137,323,135 | T/A | — | uncertain significance |
| rs1775077792 | 6:137,323,176 | G/A | — | uncertain significance |
| rs781457629 | 6:137,323,237 | C/T | — | uncertain significance |
| rs867814689 | 6:137,323,251 | A/C | — | uncertain significance |
| rs143552862 | 6:137,323,395 | T/C | — | uncertain significance |
| rs756416263 | 6:137,325,786 | A/G | — | uncertain significance |
| rs139282838 | 6:137,325,788 | G/A | synonymous variant | — |
| rs748789284 | 6:137,329,755 | C/A | — | uncertain significance |
| rs201628125 | 6:137,329,781 | G/A | — | uncertain significance |
| rs369006457 | 6:137,329,796 | C/T | — | uncertain significance |
| rs2548152688 | 6:137,329,828 | T/C | — | uncertain significance |
| rs143005532 | 6:137,330,486 | C/T | missense variant | — |
| rs137875834 | 6:137,331,095 | G/C | intron variant | — |
| rs1775488772 | 6:137,332,471 | T/C | — | uncertain significance |
| rs1775493299 | 6:137,332,536 | G/C | — | uncertain significance |
| rs2548154982 | 6:137,332,537 | T/C | — | uncertain significance |
| rs138995272 | 6:137,332,546 | T/C | — | uncertain significance |
| rs2548158551 | 6:137,338,123 | T/A | — | uncertain significance |
| rs565601068 | 6:137,338,159 | G/A | — | uncertain significance |
| rs1184860 | 6:137,340,604 | C/G | — | — |
| rs1167846 | 6:137,343,720 | T/C | intron variant | — |
| rs1167849 | 6:137,349,025 | A/G | intron variant | — |
| rs1776838755 | 6:137,365,811 | G/T | — | uncertain significance |
| rs1187966063 | 6:137,365,819 | G/A | — | uncertain significance |
| rs1049036368 | 6:137,365,822 | G/T | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.