TEX2
testis expressed 2
Summary
Predicted to enable lipid binding activity. Predicted to be involved in signal transduction and sphingolipid metabolic process. Predicted to be located in membrane. Predicted to be active in endoplasmic reticulum. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants60 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs1280248302 | 17:62,226,361 | C/A | — | uncertain significance |
| rs2509217987 | 17:62,226,442 | C/T | — | uncertain significance |
| rs371512535 | 17:62,228,244 | T/G | — | uncertain significance |
| rs368259551 | 17:62,230,327 | G/A | — | uncertain significance |
| rs757161133 | 17:62,232,209 | C/G | — | uncertain significance |
| rs9900607 | 17:62,235,843 | C/A | — | — |
| rs775710734 | 17:62,238,233 | T/C | — | uncertain significance |
| rs2509269188 | 17:62,238,282 | C/T | — | uncertain significance |
| rs774508538 | 17:62,248,523 | G/T | — | uncertain significance |
| rs2509330045 | 17:62,254,770 | C/G | — | uncertain significance |
| rs755414173 | 17:62,265,545 | G/A | — | uncertain significance |
| rs527473632 | 17:62,265,620 | C/T | — | uncertain significance |
| rs764550614 | 17:62,265,627 | G/C | — | uncertain significance |
| rs780677398 | 17:62,265,727 | G/A | — | uncertain significance |
| rs552153537 | 17:62,265,737 | C/T | — | uncertain significance |
| rs750661894 | 17:62,265,742 | G/A | — | uncertain significance |
| rs80126959 | 17:62,269,200 | A/G | — | — |
| rs150878483 | 17:62,270,960 | G/A | — | uncertain significance |
| rs2032371067 | 17:62,270,975 | G/T | — | uncertain significance |
| rs938294341 | 17:62,271,060 | T/C | — | uncertain significance |
| rs201441573 | 17:62,271,077 | C/T | — | likely benign |
| rs2509396201 | 17:62,271,111 | C/T | — | uncertain significance |
| rs2509396657 | 17:62,271,188 | C/A | — | uncertain significance |
| rs1312121433 | 17:62,271,221 | C/T | — | uncertain significance |
| rs747185675 | 17:62,272,277 | A/G | — | uncertain significance |
| rs1598165163 | 17:62,272,311 | G/A | — | uncertain significance |
| rs369287988 | 17:62,289,983 | C/T | — | likely benign |
| rs372604630 | 17:62,290,090 | A/C | — | uncertain significance |
| rs1485148498 | 17:62,290,107 | G/C | — | uncertain significance |
| rs1295566420 | 17:62,290,140 | T/C | — | uncertain significance |
| rs1419685509 | 17:62,290,182 | C/T | — | uncertain significance |
| rs560636738 | 17:62,290,230 | C/T | — | uncertain significance |
| rs144995761 | 17:62,290,248 | G/C | — | uncertain significance |
| rs138840560 | 17:62,290,276 | A/T | — | uncertain significance |
| rs782479358 | 17:62,290,289 | G/A | — | likely benign |
| rs782705677 | 17:62,290,299 | C/A | — | uncertain significance |
| rs1488354919 | 17:62,290,322 | C/A | — | uncertain significance |
| rs150703362 | 17:62,290,439 | A/G | — | uncertain significance |
| rs201073917 | 17:62,290,486 | G/C | — | uncertain significance |
| rs2509463514 | 17:62,290,500 | T/C | — | uncertain significance |
| rs2033063207 | 17:62,290,544 | C/G | — | uncertain significance |
| rs199711081 | 17:62,290,638 | C/T | — | uncertain significance |
| rs2509465111 | 17:62,290,689 | C/T | — | uncertain significance |
| rs782316817 | 17:62,290,732 | T/G | — | uncertain significance |
| rs541588191 | 17:62,290,821 | G/C | — | uncertain significance |
| rs1011874215 | 17:62,290,944 | G/A | — | uncertain significance |
| rs782624840 | 17:62,290,956 | C/T | — | uncertain significance |
| rs1329652243 | 17:62,291,064 | T/C | — | likely benign |
| rs782395498 | 17:62,291,081 | G/C | — | uncertain significance |
| rs368868113 | 17:62,291,163 | A/T | — | uncertain significance |
| rs2033102152 | 17:62,291,184 | A/T | — | uncertain significance |
| rs782769267 | 17:62,291,214 | G/C | — | uncertain significance |
| rs781872151 | 17:62,291,241 | T/G | — | uncertain significance |
| rs782338359 | 17:62,291,282 | G/A | — | uncertain significance |
| rs201071171 | 17:62,291,306 | G/A | — | uncertain significance |
| rs782469214 | 17:62,291,322 | C/T | — | likely benign |
| rs374122281 | 17:62,291,451 | C/T | — | uncertain significance |
| rs371346792 | 17:62,291,532 | G/A | — | uncertain significance |
| rs562126347 | 17:62,291,535 | T/C | — | uncertain significance |
| rs147803922 | 17:62,306,084 | G/A | intron variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.