TLR10
toll like receptor 10
Summary
The protein encoded by this gene is a member of the Toll-like receptor (TLR) family which plays a fundamental role in pathogen recognition and activation of innate immunity. TLRs are highly conserved from Drosophila to humans and share structural and functional similarities. They recognize pathogen-associated molecular patterns (PAMPs) that are expressed on infectious agents, and mediate the production of cytokines necessary for the development of effective immunity. The various TLRs exhibit different patterns of expression. This gene is most highly expressed in lymphoid tissues such as spleen, lymph node, thymus, and tonsil. Multiple alternatively spliced transcript variants which encode different protein isoforms have been found for this gene. [provided by RefSeq, Aug 2010]
Known Variants60 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs899423584 | 4:38,773,689 | C/T | — | uncertain significance |
| rs4504265 | 4:38,773,865 | G/T | 3 prime UTR variant | — |
| rs9715769 | 4:38,774,489 | A/C | 3 prime UTR variant | — |
| rs1724741986 | 4:38,774,804 | A/T | — | uncertain significance |
| rs4129008 | 4:38,774,816 | C/T | — | likely benign |
| rs572869482 | 4:38,774,871 | C/T | — | uncertain significance |
| rs755738760 | 4:38,774,880 | T/C | — | uncertain significance |
| rs4129009 | 4:38,774,889 | T/A | missense variant | — |
| rs2529429657 | 4:38,774,895 | C/T | — | uncertain significance |
| rs777851196 | 4:38,774,907 | C/T | — | uncertain significance |
| rs149895872 | 4:38,774,957 | T/C | — | likely benign |
| rs755861523 | 4:38,774,994 | T/C | — | uncertain significance |
| rs144520113 | 4:38,775,029 | A/G | — | uncertain significance |
| rs375536529 | 4:38,775,039 | T/C | — | uncertain significance |
| rs747963911 | 4:38,775,043 | A/T | — | uncertain significance |
| rs375772822 | 4:38,775,213 | G/A | — | uncertain significance |
| rs777366922 | 4:38,775,381 | C/G | — | uncertain significance |
| rs11466659 | 4:38,775,405 | G/A | — | benign |
| rs149045737 | 4:38,775,502 | G/A | — | benign |
| rs944813738 | 4:38,775,632 | G/A | — | uncertain significance |
| rs11466658 | 4:38,775,639 | G/C | missense variant | — |
| rs149319935 | 4:38,775,656 | G/T | — | uncertain significance |
| rs778053938 | 4:38,775,662 | A/T | — | uncertain significance |
| rs41305286 | 4:38,775,706 | G/A | — | benign |
| rs377071090 | 4:38,775,941 | A/G | — | uncertain significance |
| rs772298337 | 4:38,776,020 | G/C | — | uncertain significance |
| rs11466655 | 4:38,776,070 | C/T | missense variant | — |
| rs1724892648 | 4:38,776,080 | T/C | — | uncertain significance |
| rs62617795 | 4:38,776,104 | G/A | — | benign |
| rs368701488 | 4:38,776,106 | A/G | — | uncertain significance |
| rs11096955 | 4:38,776,107 | T/G | missense variant | — |
| rs11096956 | 4:38,776,180 | C/A | synonymous variant | — |
| rs754215915 | 4:38,776,220 | A/G | — | uncertain significance |
| rs141371489 | 4:38,776,222 | G/C | — | uncertain significance |
| rs11466653 | 4:38,776,235 | A/G | missense variant | — |
| rs765754385 | 4:38,776,254 | A/C | — | uncertain significance |
| rs11466652 | 4:38,776,303 | T/C | synonymous variant | — |
| rs938309459 | 4:38,776,322 | G/A | — | uncertain significance |
| rs2529443318 | 4:38,776,329 | A/T | — | uncertain significance |
| rs145992369 | 4:38,776,337 | A/T | — | uncertain significance |
| rs903992887 | 4:38,776,394 | T/C | — | uncertain significance |
| rs138428918 | 4:38,776,431 | G/A | — | uncertain significance |
| rs368542091 | 4:38,776,437 | G/T | — | uncertain significance |
| rs1266272027 | 4:38,776,472 | A/G | — | uncertain significance |
| rs11096957 | 4:38,776,491 | T/G | missense variant | — |
| rs376747590 | 4:38,776,590 | G/A | — | uncertain significance |
| rs11466649 | 4:38,776,725 | C/A | missense variant | — |
| rs149359474 | 4:38,776,812 | T/G | — | uncertain significance |
| rs1191784439 | 4:38,776,815 | G/A | — | uncertain significance |
| rs192727806 | 4:38,776,904 | A/C | — | uncertain significance |
| rs138645932 | 4:38,776,925 | T/C | — | likely benign |
| rs11466648 | 4:38,776,942 | T/C | — | benign |
| rs371000369 | 4:38,777,042 | T/G | — | uncertain significance |
| rs10856837 | 4:38,777,059 | C/A | synonymous variant | — |
| rs1201664038 | 4:38,777,082 | C/T | — | uncertain significance |
| rs10856838 | 4:38,777,173 | A/T | synonymous variant | — |
| rs10856839 | 4:38,777,236 | T/G | 5 prime UTR variant | — |
| rs11466617 | 4:38,780,471 | T/C | intron variant | — |
| rs182072481 | 4:38,782,121 | C/A | intron variant | — |
| rs10004195 | 4:38,784,724 | T/A | regulatory region variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.