TMEM131L
transmembrane 131 like
Summary
Involved in negative regulation of canonical Wnt signaling pathway and negative regulation of immature T cell proliferation in thymus. Located in cytoplasm and plasma membrane. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants117 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs7687559 | 4:154,385,925 | G/C | upstream gene variant | — |
| rs745913297 | 4:154,387,557 | G/T | — | uncertain significance |
| rs1269264340 | 4:154,387,566 | G/A | — | uncertain significance |
| rs1337086690 | 4:154,387,568 | C/T | — | uncertain significance |
| rs1382127593 | 4:154,387,593 | C/G | — | uncertain significance |
| rs1730752418 | 4:154,387,637 | C/G | — | uncertain significance |
| rs78441178 | 4:154,388,363 | C/T | — | uncertain significance |
| rs116269527 | 4:154,397,537 | A/G | intron variant | — |
| rs2016847 | 4:154,402,835 | C/T | regulatory region variant | — |
| rs10034572 | 4:154,416,418 | C/G | intron variant | — |
| rs80259713 | 4:154,420,606 | G/A | intron variant | — |
| rs113472668 | 4:154,430,376 | G/A | intron variant | — |
| rs34536783 | 4:154,441,151 | T/G | — | — |
| rs79403652 | 4:154,457,001 | T/A | intron variant | — |
| rs2014511 | 4:154,457,519 | G/A | regulatory region variant | — |
| rs78947501 | 4:154,459,955 | G/C | intron variant | — |
| rs201330911 | 4:154,471,243 | T/G | — | uncertain significance |
| rs1482067670 | 4:154,476,986 | G/A | — | uncertain significance |
| rs139597924 | 4:154,477,046 | C/T | — | uncertain significance |
| rs530138329 | 4:154,479,429 | G/A | — | uncertain significance |
| rs991952644 | 4:154,479,433 | A/C | — | uncertain significance |
| rs1481090537 | 4:154,479,438 | C/T | — | uncertain significance |
| rs759428830 | 4:154,479,480 | T/C | — | uncertain significance |
| rs553100868 | 4:154,502,013 | A/C | — | uncertain significance |
| rs188378248 | 4:154,502,692 | C/T | — | uncertain significance |
| rs367812835 | 4:154,504,738 | G/C | — | uncertain significance |
| rs891288554 | 4:154,504,822 | A/G | — | likely benign |
| rs375611056 | 4:154,505,987 | C/T | — | uncertain significance |
| rs757761062 | 4:154,506,641 | T/G | — | uncertain significance |
| rs1730642252 | 4:154,506,666 | C/G | — | uncertain significance |
| rs200880434 | 4:154,506,734 | C/T | — | uncertain significance |
| rs1730690278 | 4:154,507,379 | C/T | — | uncertain significance |
| rs1393955141 | 4:154,507,493 | T/C | — | uncertain significance |
| rs1730796628 | 4:154,508,935 | G/T | — | uncertain significance |
| rs149514201 | 4:154,510,150 | A/G | — | uncertain significance |
| rs577605054 | 4:154,510,152 | G/A | — | uncertain significance |
| rs766472443 | 4:154,512,228 | G/A | — | uncertain significance |
| rs764052822 | 4:154,512,246 | A/C | — | uncertain significance |
| rs754067777 | 4:154,512,255 | A/G | — | uncertain significance |
| rs201309930 | 4:154,512,285 | G/A | — | uncertain significance |
| rs368760997 | 4:154,512,293 | G/T | — | uncertain significance |
| rs200596505 | 4:154,512,323 | G/A | — | uncertain significance |
| rs761806542 | 4:154,512,332 | C/G | — | uncertain significance |
| rs762624260 | 4:154,512,339 | G/A | — | likely benign |
| rs752264104 | 4:154,513,630 | A/C | — | uncertain significance |
| rs772989113 | 4:154,513,714 | C/A | — | uncertain significance |
| rs1478268040 | 4:154,513,729 | C/G | — | uncertain significance |
| rs373784376 | 4:154,514,956 | G/A | — | uncertain significance |
| rs776220044 | 4:154,514,963 | T/G | — | uncertain significance |
| rs2533867659 | 4:154,514,968 | A/G | — | uncertain significance |
| rs1160924386 | 4:154,514,989 | G/T | — | uncertain significance |
| rs766793297 | 4:154,515,000 | C/G | — | uncertain significance |
| rs376598929 | 4:154,517,410 | G/A | — | uncertain significance |
| rs771497113 | 4:154,517,438 | G/T | — | uncertain significance |
| rs767816688 | 4:154,517,443 | C/G | — | uncertain significance |
| rs2534018095 | 4:154,519,753 | C/A | — | uncertain significance |
| rs539791243 | 4:154,519,765 | T/C | — | uncertain significance |
| rs371805678 | 4:154,519,772 | C/T | — | likely benign |
| rs1403175288 | 4:154,519,869 | A/C | — | uncertain significance |
| rs762917240 | 4:154,519,871 | G/A | — | uncertain significance |
| rs2534119478 | 4:154,523,341 | G/T | — | uncertain significance |
| rs146948220 | 4:154,523,343 | A/T | — | uncertain significance |
| rs367657558 | 4:154,523,375 | A/G | — | uncertain significance |
| rs1469316290 | 4:154,523,408 | A/G | — | uncertain significance |
| rs1731927225 | 4:154,523,828 | C/T | — | uncertain significance |
| rs181124529 | 4:154,523,854 | T/C | — | uncertain significance |
| rs562825838 | 4:154,524,488 | C/G | — | uncertain significance |
| rs1240174563 | 4:154,524,510 | A/G | — | uncertain significance |
| rs201606828 | 4:154,524,961 | T/C | — | uncertain significance |
| rs768726330 | 4:154,524,978 | T/A | — | uncertain significance |
| rs1041442313 | 4:154,525,021 | C/G | — | uncertain significance |
| rs1732024182 | 4:154,525,031 | C/T | — | uncertain significance |
| rs148369229 | 4:154,525,041 | C/G | — | uncertain significance |
| rs148745131 | 4:154,525,072 | G/A | — | uncertain significance |
| rs748142322 | 4:154,525,079 | A/G | — | uncertain significance |
| rs758028166 | 4:154,525,295 | A/G | — | uncertain significance |
| rs1367691070 | 4:154,525,321 | T/G | — | uncertain significance |
| rs781629334 | 4:154,525,329 | T/G | — | uncertain significance |
| rs200721684 | 4:154,525,420 | C/T | — | uncertain significance |
| rs17030219 | 4:154,525,446 | A/C | — | benign |
| rs146931484 | 4:154,525,471 | C/T | — | uncertain significance |
| rs143102826 | 4:154,533,467 | A/G | — | uncertain significance |
| rs751129486 | 4:154,533,508 | A/G | — | uncertain significance |
| rs1378781160 | 4:154,541,953 | G/A | — | uncertain significance |
| rs750418588 | 4:154,541,963 | A/C | — | uncertain significance |
| rs766961205 | 4:154,541,980 | A/G | — | uncertain significance |
| rs375699910 | 4:154,542,008 | A/G | — | uncertain significance |
| rs768548948 | 4:154,542,867 | G/A | — | uncertain significance |
| rs959648311 | 4:154,542,879 | A/G | — | uncertain significance |
| rs199606904 | 4:154,542,903 | T/G | — | uncertain significance |
| rs35018723 | 4:154,542,906 | A/G | — | benign |
| rs759930386 | 4:154,544,082 | G/A | — | uncertain significance |
| rs901039076 | 4:154,544,116 | G/A | — | uncertain significance |
| rs754748153 | 4:154,544,130 | G/A | — | uncertain significance |
| rs781143708 | 4:154,544,131 | G/T | — | uncertain significance |
| rs769545314 | 4:154,544,136 | G/A | — | uncertain significance |
| rs1256350414 | 4:154,544,139 | C/T | — | uncertain significance |
| rs765879905 | 4:154,544,140 | G/A | — | uncertain significance |
| rs148556115 | 4:154,544,148 | C/T | — | uncertain significance |
| rs923502545 | 4:154,544,149 | G/A | — | uncertain significance |
Showing 100 of 117 variants. Use the SNP search for the full list.
Gene information from NCBI Gene. Variant classifications from ClinVar.