IL1RAPL2
interleukin 1 receptor accessory protein like 2
Summary
The protein encoded by this gene is a member of the interleukin 1 receptor family. This protein is similar to the interleukin 1 accessory proteins, and is most closely related to interleukin 1 receptor accessory protein-like 1 (IL1RAPL1). This gene and IL1RAPL1 are located at a region on chromosome X that is associated with X-linked non-syndromic cognitive disability. [provided by RefSeq, Jul 2008]
Known Variants27 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs148390300 | X:103,903,610 | C/T | — | conflicting classifications of pathogenicity |
| rs771962632 | X:103,903,644 | C/G | — | uncertain significance |
| rs139525400 | X:103,903,659 | T/C | — | uncertain significance |
| rs185459423 | X:103,969,256 | A/T | intron variant | — |
| rs12688128 | X:103,992,452 | T/A | — | — |
| rs144175494 | X:104,440,391 | C/T | — | likely benign |
| rs1242930443 | X:104,512,088 | G/A | — | uncertain significance |
| rs974154443 | X:104,512,112 | A/C | — | uncertain significance |
| rs376297335 | X:104,728,296 | C/T | — | likely benign |
| rs755013837 | X:104,728,318 | C/A | — | uncertain significance |
| rs954042302 | X:104,728,349 | A/G | — | uncertain significance |
| rs210545 | X:104,880,023 | C/T | regulatory region variant | — |
| rs2213321 | X:104,938,679 | C/T | intron variant | — |
| rs3764765 | X:104,992,963 | T/C | — | benign |
| rs147084511 | X:104,992,994 | A/G | — | uncertain significance |
| rs369182827 | X:104,993,048 | T/C | — | likely benign |
| rs2544726089 | X:104,993,057 | T/C | — | uncertain significance |
| rs2544728954 | X:104,999,179 | G/C | — | uncertain significance |
| rs773209977 | X:104,999,323 | G/T | — | uncertain significance |
| rs371650196 | X:105,011,081 | G/T | — | uncertain significance |
| rs372593455 | X:105,011,149 | A/G | — | uncertain significance |
| rs377437750 | X:105,011,170 | G/A | — | uncertain significance |
| rs748143301 | X:105,011,247 | T/A | — | uncertain significance |
| rs757802661 | X:105,011,382 | G/T | — | uncertain significance |
| rs771019228 | X:105,011,472 | G/A | — | likely benign |
| rs2544734998 | X:105,011,499 | G/C | — | uncertain significance |
| rs368014818 | X:105,011,509 | A/G | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.