TEX11
testis expressed 11
Summary
This gene is X-linked and is expressed in only male germ cells. Two alternatively spliced transcript variants encoding distinct isoforms have been found for this gene. [provided by RefSeq, Jul 2008]
Known Variants62 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs5980712 | X:69,733,949 | C/G | intergenic variant | — |
| rs2087851500 | X:69,748,969 | A/C | — | uncertain significance |
| rs374729936 | X:69,748,970 | T/C | — | uncertain significance |
| rs2519943110 | X:69,749,704 | T/C | — | uncertain significance |
| rs374367768 | X:69,749,756 | C/T | — | uncertain significance |
| rs201633202 | X:69,749,796 | G/A | — | likely benign |
| rs2147923995 | X:69,749,802 | C/A | — | pathogenic |
| rs16991177 | X:69,772,000 | A/C | — | benign |
| rs2088223979 | X:69,772,032 | G/C | — | uncertain significance |
| rs144951375 | X:69,772,048 | C/T | — | likely benign |
| rs376114732 | X:69,772,051 | C/T | — | likely benign |
| rs202136447 | X:69,773,162 | T/C | — | likely benign |
| rs1210179902 | X:69,773,179 | T/A | — | uncertain significance |
| rs1485266259 | X:69,773,255 | A/G | — | uncertain significance |
| rs2519988538 | X:69,773,256 | T/C | — | uncertain significance |
| rs1177646259 | X:69,774,493 | G/T | — | likely benign |
| rs200139216 | X:69,774,548 | A/G | — | likely benign |
| rs143644139 | X:69,774,549 | C/A | — | uncertain significance |
| rs140984555 | X:69,825,271 | C/T | missense variant | pathogenic |
| rs139166251 | X:69,829,006 | G/C | — | uncertain significance |
| rs200375710 | X:69,830,364 | C/T | — | conflicting classifications of pathogenicity |
| rs2147552254 | X:69,843,798 | A/C | — | pathogenic |
| rs370307636 | X:69,849,476 | G/C | — | likely benign |
| rs1220744701 | X:69,849,538 | A/G | — | uncertain significance |
| rs147097227 | X:69,849,558 | T/G | — | uncertain significance |
| rs1351844566 | X:69,849,565 | A/C | — | uncertain significance |
| rs761532491 | X:69,849,589 | A/G | — | likely benign |
| rs144149425 | X:69,871,310 | G/T | — | conflicting classifications of pathogenicity |
| rs2147608548 | X:69,871,403 | C/T | — | pathogenic |
| rs4844247 | X:69,890,301 | C/T | — | benign |
| rs759491904 | X:69,890,330 | T/C | — | uncertain significance |
| rs2520278960 | X:69,898,676 | C/T | — | likely benign |
| rs769718746 | X:69,898,690 | G/C | — | uncertain significance |
| rs2520279106 | X:69,898,719 | G/T | — | uncertain significance |
| rs1169164404 | X:69,902,556 | A/G | — | uncertain significance |
| rs2147658893 | X:69,902,674 | C/A | — | pathogenic |
| rs374217762 | X:69,942,497 | G/T | — | uncertain significance |
| rs575754903 | X:69,945,139 | C/T | — | benign |
| rs372375453 | X:69,945,193 | C/T | — | uncertain significance |
| rs775098071 | X:69,964,026 | G/A | — | likely benign |
| rs2090753181 | X:69,964,055 | A/G | — | uncertain significance |
| rs5936980 | X:69,982,713 | A/G | intron variant | — |
| rs4844261 | X:69,994,878 | T/G | intron variant | — |
| rs146176796 | X:70,050,184 | C/T | intron variant | — |
| rs779629000 | X:70,053,433 | T/C | — | likely benign |
| rs375000923 | X:70,072,907 | C/T | — | uncertain significance |
| rs1296061122 | X:70,072,921 | C/T | — | uncertain significance |
| rs143246552 | X:70,072,943 | T/C | missense variant | pathogenic |
| rs181134374 | X:70,072,982 | T/G | — | benign |
| rs773083176 | X:70,072,985 | C/T | — | likely benign |
| rs150818139 | X:70,073,000 | G/A | — | benign |
| rs147088100 | X:70,073,098 | G/A | splice region variant | pathogenic |
| rs767787700 | X:70,073,166 | T/A | — | uncertain significance |
| rs2521200388 | X:70,073,176 | C/T | — | uncertain significance |
| rs1423488984 | X:70,080,739 | C/A | — | uncertain significance |
| rs750415628 | X:70,093,155 | A/T | — | benign |
| rs141951098 | X:70,099,942 | C/G | — | uncertain significance |
| rs372962201 | X:70,099,966 | T/G | — | likely benign |
| rs13441058 | X:70,108,862 | G/C | intron variant | — |
| rs13441059 | X:70,108,889 | G/A | intron variant | — |
| rs186347618 | X:70,117,073 | A/T | intron variant | — |
| rs62608084 | X:70,125,103 | G/A | intron variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.