TMEM266
transmembrane protein 266
Summary
Enables protein homodimerization activity. Predicted to be involved in transmembrane transport. Located in cytosol; dendrite; and plasma membrane. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants39 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs76667145 | 15:76,355,247 | C/T | upstream gene variant | — |
| rs114849949 | 15:76,379,202 | T/G | intron variant | — |
| rs184897488 | 15:76,385,365 | T/A | — | — |
| rs370445042 | 15:76,430,082 | A/G | — | uncertain significance |
| rs540647010 | 15:76,430,152 | G/A | — | uncertain significance |
| rs778812089 | 15:76,430,175 | G/A | — | uncertain significance |
| rs2037616202 | 15:76,430,233 | A/G | — | uncertain significance |
| rs761044327 | 15:76,449,015 | C/G | — | uncertain significance |
| rs780642775 | 15:76,452,444 | G/T | — | uncertain significance |
| rs1490068727 | 15:76,462,158 | C/G | — | uncertain significance |
| rs761300568 | 15:76,467,950 | G/A | — | uncertain significance |
| rs772544145 | 15:76,467,993 | C/T | — | uncertain significance |
| rs6495195 | 15:76,471,282 | A/T | intron variant | — |
| rs753844829 | 15:76,484,384 | C/G | — | uncertain significance |
| rs755147854 | 15:76,484,388 | C/A | — | uncertain significance |
| rs758938634 | 15:76,484,390 | C/G | — | uncertain significance |
| rs201840892 | 15:76,496,087 | G/A | — | uncertain significance |
| rs775287535 | 15:76,496,112 | T/C | — | uncertain significance |
| rs542868398 | 15:76,496,121 | C/T | — | uncertain significance |
| rs556150508 | 15:76,496,126 | G/A | — | uncertain significance |
| rs532604457 | 15:76,496,129 | A/G | — | uncertain significance |
| rs766796985 | 15:76,496,133 | A/C | — | uncertain significance |
| rs1045857460 | 15:76,496,147 | A/C | — | uncertain significance |
| rs779070135 | 15:76,496,180 | C/A | — | uncertain significance |
| rs143570529 | 15:76,496,291 | T/C | — | uncertain significance |
| rs754961645 | 15:76,496,303 | C/T | — | uncertain significance |
| rs765232679 | 15:76,496,343 | C/T | — | uncertain significance |
| rs1240806259 | 15:76,496,355 | A/C | — | uncertain significance |
| rs371561578 | 15:76,496,370 | A/C | — | uncertain significance |
| rs759141753 | 15:76,496,407 | G/T | — | uncertain significance |
| rs2038797057 | 15:76,496,415 | G/A | — | uncertain significance |
| rs375411507 | 15:76,496,447 | C/A | — | uncertain significance |
| rs1481366012 | 15:76,496,450 | G/A | — | uncertain significance |
| rs762917837 | 15:76,496,453 | C/T | — | uncertain significance |
| rs774278839 | 15:76,496,454 | G/A | — | likely benign |
| rs776679000 | 15:76,496,557 | G/T | — | uncertain significance |
| rs1003226137 | 15:76,496,571 | T/G | — | uncertain significance |
| rs1450238917 | 15:76,496,624 | G/A | — | uncertain significance |
| rs2542945971 | 15:76,496,643 | T/C | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.