TENM2
teneurin transmembrane protein 2
Summary
Enables cell adhesion molecule binding activity and signaling receptor binding activity. Involved in retrograde trans-synaptic signaling by trans-synaptic protein complex. Located in cell-cell junction and plasma membrane. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants187 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs113221192 | 5:166,461,525 | C/T | intergenic variant | — |
| rs2937573 | 5:166,471,198 | G/A | intergenic variant | — |
| rs6878961 | 5:166,576,254 | C/A | intergenic variant | — |
| rs7732121 | 5:166,583,598 | A/C | intergenic variant | — |
| rs17068133 | 5:166,660,911 | A/T | intergenic variant | — |
| rs4869022 | 5:166,666,654 | T/A | — | — |
| rs115605129 | 5:166,711,862 | G/A | — | likely benign |
| rs927787947 | 5:166,711,867 | C/T | — | uncertain significance |
| rs373703904 | 5:166,711,900 | T/C | — | uncertain significance |
| rs1293965002 | 5:166,711,985 | C/T | — | uncertain significance |
| rs1384950683 | 5:166,711,993 | C/T | — | uncertain significance |
| rs1302505035 | 5:166,711,994 | A/G | — | uncertain significance |
| rs768754959 | 5:166,712,011 | T/C | — | uncertain significance |
| rs1771255928 | 5:166,712,042 | G/A | — | uncertain significance |
| rs4242220 | 5:166,744,741 | T/G | intron variant | — |
| rs1946229 | 5:166,749,721 | C/G | — | — |
| rs977156 | 5:166,749,868 | C/G | — | — |
| rs747101270 | 5:166,802,263 | A/G | — | uncertain significance |
| rs202033524 | 5:166,802,316 | G/A | — | uncertain significance |
| rs2533641438 | 5:166,802,341 | G/C | — | uncertain significance |
| rs539938784 | 5:166,802,355 | C/A | — | uncertain significance |
| rs1760686562 | 5:166,802,395 | G/A | — | uncertain significance |
| rs1466072385 | 5:166,802,404 | G/T | — | uncertain significance |
| rs1330859388 | 5:166,802,464 | C/T | — | uncertain significance |
| rs1363490 | 5:166,821,663 | A/C | intron variant | — |
| rs11745240 | 5:166,832,161 | A/T | — | — |
| rs4242224 | 5:166,952,964 | C/T | intron variant | — |
| rs883323 | 5:166,987,744 | C/T | intron variant | — |
| rs12188010 | 5:166,996,466 | A/C | — | — |
| rs1549212 | 5:166,996,722 | C/T | intron variant | — |
| rs6882026 | 5:167,011,283 | C/A | intron variant | — |
| rs73803919 | 5:167,075,660 | G/A | downstream gene variant | — |
| rs577665147 | 5:167,077,052 | G/C | — | — |
| rs1459073 | 5:167,100,706 | T/C | intron variant | — |
| rs2973662 | 5:167,210,472 | A/T | — | — |
| rs1549309 | 5:167,226,979 | G/A | intron variant | — |
| rs757858208 | 5:167,303,065 | C/T | — | uncertain significance |
| rs535674876 | 5:167,379,617 | C/T | — | uncertain significance |
| rs201859793 | 5:167,379,667 | C/G | — | uncertain significance |
| rs1436837143 | 5:167,379,709 | A/G | — | uncertain significance |
| rs200992047 | 5:167,420,039 | G/A | — | likely benign |
| rs751197197 | 5:167,420,139 | G/A | — | uncertain significance |
| rs752526514 | 5:167,420,149 | C/T | — | uncertain significance |
| rs750504003 | 5:167,420,154 | C/T | — | uncertain significance |
| rs768848830 | 5:167,420,176 | C/T | — | uncertain significance |
| rs996280345 | 5:167,474,453 | A/G | — | uncertain significance |
| rs939615343 | 5:167,474,506 | G/A | — | uncertain significance |
| rs796097884 | 5:167,474,521 | G/A | — | uncertain significance |
| rs1359378253 | 5:167,474,548 | G/A | — | uncertain significance |
| rs756284185 | 5:167,489,119 | G/A | — | uncertain significance |
| rs778257205 | 5:167,489,122 | G/A | — | uncertain significance |
| rs1355770249 | 5:167,489,148 | G/T | — | uncertain significance |
| rs72824990 | 5:167,489,170 | A/G | — | likely benign |
| rs2534381489 | 5:167,489,193 | A/C | — | uncertain significance |
| rs764193780 | 5:167,489,220 | G/T | — | uncertain significance |
| rs13358864 | 5:167,500,460 | T/A | intron variant | — |
| rs371887372 | 5:167,517,603 | G/A | — | uncertain significance |
| rs776903679 | 5:167,517,748 | T/C | — | uncertain significance |
| rs745647744 | 5:167,517,760 | A/G | — | uncertain significance |
| rs1200374543 | 5:167,517,763 | C/G | — | uncertain significance |
| rs370631553 | 5:167,525,087 | G/T | — | likely benign |
| rs6867056 | 5:167,535,028 | G/T | intron variant | — |
| rs1554200966 | 5:167,545,296 | G/T | — | uncertain significance |
| rs780213706 | 5:167,545,407 | G/A | — | uncertain significance |
| rs531257360 | 5:167,545,477 | A/G | — | uncertain significance |
| rs1018268843 | 5:167,551,868 | T/A | — | uncertain significance |
| rs375848462 | 5:167,551,920 | C/G | — | uncertain significance |
| rs1265596887 | 5:167,551,932 | G/T | — | uncertain significance |
| rs368975927 | 5:167,551,951 | C/T | — | uncertain significance |
| rs573445590 | 5:167,552,001 | G/C | — | uncertain significance |
| rs773599429 | 5:167,553,807 | C/G | — | uncertain significance |
| rs1401129472 | 5:167,553,903 | G/A | — | uncertain significance |
| rs200354006 | 5:167,553,912 | G/A | — | uncertain significance |
| rs1757850239 | 5:167,589,637 | A/G | — | uncertain significance |
| rs577591482 | 5:167,589,717 | G/A | — | uncertain significance |
| rs772943929 | 5:167,589,772 | C/T | — | likely benign |
| rs759211946 | 5:167,617,419 | C/T | — | uncertain significance |
| rs372062952 | 5:167,617,429 | T/G | — | uncertain significance |
| rs369696558 | 5:167,617,461 | C/T | — | uncertain significance |
| rs755244663 | 5:167,617,464 | G/T | — | uncertain significance |
| rs2536289225 | 5:167,617,542 | T/G | — | uncertain significance |
| rs114168398 | 5:167,622,187 | T/G | — | benign |
| rs2536349157 | 5:167,622,239 | G/A | — | uncertain significance |
| rs764709973 | 5:167,622,288 | G/A | — | uncertain significance |
| rs375674029 | 5:167,625,858 | G/C | — | likely benign |
| rs752488147 | 5:167,625,899 | A/T | — | uncertain significance |
| rs373290432 | 5:167,625,931 | C/T | — | uncertain significance |
| rs2536403776 | 5:167,626,007 | C/T | — | uncertain significance |
| rs752440584 | 5:167,626,024 | G/A | — | uncertain significance |
| rs777416334 | 5:167,626,034 | G/A | — | uncertain significance |
| rs2536404119 | 5:167,626,041 | T/A | — | uncertain significance |
| rs777669148 | 5:167,626,995 | A/T | — | uncertain significance |
| rs2536419265 | 5:167,627,002 | T/G | — | uncertain significance |
| rs201582415 | 5:167,627,104 | G/A | — | uncertain significance |
| rs369152192 | 5:167,631,395 | C/G | — | uncertain significance |
| rs1762192795 | 5:167,631,458 | G/A | — | uncertain significance |
| rs560168744 | 5:167,631,618 | G/C | — | uncertain significance |
| rs184081908 | 5:167,642,095 | C/T | — | uncertain significance |
| rs200820930 | 5:167,642,133 | C/T | — | uncertain significance |
| rs370122768 | 5:167,642,137 | T/C | — | uncertain significance |
Showing 100 of 187 variants. Use the SNP search for the full list.
Gene information from NCBI Gene. Variant classifications from ClinVar.