TMEM131
transmembrane protein 131
Summary
Enables collagen binding activity. Involved in collagen biosynthetic process. Predicted to be active in membrane. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants95 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs1043164235 | 2:98,373,568 | C/A | — | uncertain significance |
| rs2482869488 | 2:98,373,569 | T/C | — | uncertain significance |
| rs201320556 | 2:98,373,584 | G/A | — | uncertain significance |
| rs776186043 | 2:98,375,375 | G/C | — | uncertain significance |
| rs377067837 | 2:98,375,499 | C/T | — | uncertain significance |
| rs370135727 | 2:98,375,500 | G/A | — | likely benign |
| rs777279725 | 2:98,376,117 | C/A | — | uncertain significance |
| rs1041074642 | 2:98,376,145 | C/T | — | uncertain significance |
| rs200149921 | 2:98,376,207 | C/G | — | uncertain significance |
| rs368653296 | 2:98,377,077 | A/C | — | uncertain significance |
| rs1678784148 | 2:98,377,083 | G/A | — | uncertain significance |
| rs887852724 | 2:98,377,147 | T/G | — | uncertain significance |
| rs762513187 | 2:98,377,150 | C/T | — | uncertain significance |
| rs2482920877 | 2:98,377,286 | C/A | — | uncertain significance |
| rs756049755 | 2:98,377,297 | G/C | — | uncertain significance |
| rs1454589542 | 2:98,377,321 | G/A | — | uncertain significance |
| rs375244518 | 2:98,377,329 | C/A | — | uncertain significance |
| rs758951140 | 2:98,377,354 | T/C | — | likely benign |
| rs201851542 | 2:98,378,534 | C/T | — | uncertain significance |
| rs777389956 | 2:98,378,537 | C/T | — | uncertain significance |
| rs201313610 | 2:98,378,573 | G/A | — | uncertain significance |
| rs373750674 | 2:98,378,576 | G/C | — | uncertain significance |
| rs2482941090 | 2:98,378,631 | T/C | — | uncertain significance |
| rs775517653 | 2:98,382,601 | C/T | — | uncertain significance |
| rs931922389 | 2:98,382,666 | T/C | — | uncertain significance |
| rs775635959 | 2:98,382,675 | G/A | — | uncertain significance |
| rs1338758114 | 2:98,382,688 | C/T | — | uncertain significance |
| rs751994220 | 2:98,382,726 | C/T | — | uncertain significance |
| rs181629538 | 2:98,382,952 | T/C | — | uncertain significance |
| rs559966387 | 2:98,383,014 | A/T | — | uncertain significance |
| rs201940321 | 2:98,408,924 | C/G | — | uncertain significance |
| rs375466644 | 2:98,408,942 | T/C | — | uncertain significance |
| rs771438042 | 2:98,409,022 | G/A | — | uncertain significance |
| rs1680552472 | 2:98,409,050 | C/T | — | uncertain significance |
| rs2483249091 | 2:98,409,071 | G/C | — | uncertain significance |
| rs2483249299 | 2:98,409,082 | G/A | — | uncertain significance |
| rs200135228 | 2:98,409,103 | G/C | — | uncertain significance |
| rs1680561307 | 2:98,409,170 | T/A | — | uncertain significance |
| rs776303550 | 2:98,409,322 | T/C | — | uncertain significance |
| rs985230490 | 2:98,409,411 | C/A | — | uncertain significance |
| rs768383002 | 2:98,409,913 | C/T | — | uncertain significance |
| rs200619760 | 2:98,411,409 | T/C | — | uncertain significance |
| rs1244911191 | 2:98,411,548 | A/G | — | likely benign |
| rs571086253 | 2:98,412,805 | G/T | — | uncertain significance |
| rs200740333 | 2:98,412,847 | T/C | — | uncertain significance |
| rs958430427 | 2:98,413,354 | G/A | — | uncertain significance |
| rs536140604 | 2:98,417,056 | T/C | — | — |
| rs780774901 | 2:98,418,360 | T/G | — | uncertain significance |
| rs896579919 | 2:98,418,957 | T/C | — | uncertain significance |
| rs370794667 | 2:98,418,972 | G/A | — | uncertain significance |
| rs1681089764 | 2:98,419,134 | G/T | — | uncertain significance |
| rs145516416 | 2:98,419,146 | T/C | — | uncertain significance |
| rs762090529 | 2:98,419,155 | C/T | — | uncertain significance |
| rs374617299 | 2:98,419,156 | G/A | — | uncertain significance |
| rs2483355330 | 2:98,419,168 | G/C | — | uncertain significance |
| rs1252539364 | 2:98,419,182 | G/A | — | uncertain significance |
| rs754544211 | 2:98,419,212 | T/C | — | uncertain significance |
| rs778394980 | 2:98,419,219 | G/T | — | uncertain significance |
| rs373324249 | 2:98,422,075 | C/T | — | uncertain significance |
| rs369519862 | 2:98,422,121 | G/C | — | uncertain significance |
| rs368760372 | 2:98,422,162 | T/C | — | uncertain significance |
| rs752955433 | 2:98,426,171 | C/T | — | uncertain significance |
| rs1681467809 | 2:98,426,215 | G/C | — | uncertain significance |
| rs756389842 | 2:98,427,613 | A/T | — | uncertain significance |
| rs1681532009 | 2:98,427,641 | T/C | — | uncertain significance |
| rs772144953 | 2:98,427,676 | T/C | — | uncertain significance |
| rs762326375 | 2:98,427,687 | T/C | — | likely benign |
| rs372870572 | 2:98,428,926 | G/T | — | uncertain significance |
| rs138984698 | 2:98,428,948 | T/C | — | uncertain significance |
| rs2104966839 | 2:98,428,954 | C/A | — | uncertain significance |
| rs763239439 | 2:98,428,985 | C/T | — | uncertain significance |
| rs773200720 | 2:98,429,176 | T/C | — | uncertain significance |
| rs2483449939 | 2:98,429,179 | A/G | — | uncertain significance |
| rs772134560 | 2:98,430,517 | T/C | — | uncertain significance |
| rs200161087 | 2:98,430,837 | T/A | — | uncertain significance |
| rs181236597 | 2:98,431,746 | T/C | — | uncertain significance |
| rs187747732 | 2:98,435,150 | G/A | — | uncertain significance |
| rs376535762 | 2:98,435,154 | T/C | — | uncertain significance |
| rs1181391047 | 2:98,435,177 | C/T | — | uncertain significance |
| rs775429376 | 2:98,460,627 | T/C | — | uncertain significance |
| rs773610584 | 2:98,504,569 | C/T | — | uncertain significance |
| rs760959147 | 2:98,504,570 | G/A | — | uncertain significance |
| rs182482858 | 2:98,506,529 | T/C | intron variant | — |
| rs145825688 | 2:98,525,134 | A/G | — | uncertain significance |
| rs752938880 | 2:98,543,921 | C/A | — | uncertain significance |
| rs149366039 | 2:98,543,945 | C/T | — | benign |
| rs35589428 | 2:98,565,743 | T/C | intron variant | — |
| rs7564773 | 2:98,571,084 | A/T | — | — |
| rs114673995 | 2:98,585,266 | G/A | intron variant | — |
| rs953320 | 2:98,606,770 | T/C | intron variant | — |
| rs993335569 | 2:98,611,974 | G/C | — | uncertain significance |
| rs970319318 | 2:98,611,992 | G/A | — | uncertain significance |
| rs923677370 | 2:98,612,043 | G/A | — | uncertain significance |
| rs889603986 | 2:98,612,088 | G/T | — | uncertain significance |
| rs1040952100 | 2:98,612,113 | C/G | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.