STRN
striatin
Summary
Enables armadillo repeat domain binding activity; nuclear estrogen receptor binding activity; and protein phosphatase 2A binding activity. Involved in Wnt signaling pathway and negative regulation of cell population proliferation. Located in bicellular tight junction. Part of FAR/SIN/STRIPAK complex. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants68 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs62132520 | 2:37,076,498 | A/C | — | benign |
| rs62132521 | 2:37,076,594 | T/C | — | benign |
| rs989193193 | 2:37,076,622 | C/T | — | uncertain significance |
| rs373594803 | 2:37,076,754 | T/C | — | uncertain significance |
| rs758649599 | 2:37,076,930 | G/C | — | uncertain significance |
| rs723674 | 2:37,077,015 | C/A | — | benign |
| rs723673 | 2:37,077,176 | G/A | — | benign |
| rs28593131 | 2:37,078,354 | G/A | — | benign |
| rs28701005 | 2:37,078,388 | G/A | — | benign |
| rs1861433 | 2:37,082,034 | A/G | — | benign |
| rs199834082 | 2:37,082,414 | C/T | — | uncertain significance |
| rs998321 | 2:37,082,695 | T/C | — | benign |
| rs2717496 | 2:37,084,717 | T/C | — | benign |
| rs143539814 | 2:37,085,047 | T/G | — | uncertain significance |
| rs2465599878 | 2:37,085,076 | C/G | — | uncertain significance |
| rs202125881 | 2:37,085,130 | G/A | — | uncertain significance |
| rs2717498 | 2:37,085,474 | G/A | — | benign |
| rs2717499 | 2:37,087,940 | A/G | — | benign |
| rs2540935 | 2:37,088,083 | C/T | — | benign |
| rs112595766 | 2:37,088,298 | T/C | — | uncertain significance |
| rs375947333 | 2:37,088,364 | T/C | — | uncertain significance |
| rs75915538 | 2:37,094,804 | C/T | — | benign |
| rs2540923 | 2:37,094,945 | A/G | upstream gene variant | benign |
| rs201385587 | 2:37,094,963 | G/C | — | uncertain significance |
| rs6752845 | 2:37,095,139 | G/C | — | benign |
| rs17020005 | 2:37,095,206 | T/C | — | benign |
| rs2160379 | 2:37,096,970 | C/T | — | benign |
| rs2110942 | 2:37,097,009 | T/C | — | benign |
| rs761655417 | 2:37,105,059 | T/C | — | uncertain significance |
| rs573694681 | 2:37,105,119 | G/C | — | uncertain significance |
| rs17020024 | 2:37,105,178 | G/A | — | benign |
| rs2691106 | 2:37,111,045 | A/T | — | benign |
| rs2465668162 | 2:37,111,080 | T/C | — | uncertain significance |
| rs770601942 | 2:37,111,083 | G/A | — | uncertain significance |
| rs541490607 | 2:37,111,108 | G/C | — | uncertain significance |
| rs375649141 | 2:37,111,110 | C/T | — | uncertain significance |
| rs756037358 | 2:37,111,186 | C/A | — | uncertain significance |
| rs189424401 | 2:37,120,677 | G/A | intron variant | — |
| rs763857008 | 2:37,121,145 | C/T | — | uncertain significance |
| rs2003585 | 2:37,123,383 | T/C | intron variant | — |
| rs2691112 | 2:37,124,755 | T/C | intron variant | — |
| rs75193488 | 2:37,126,651 | A/C | — | benign |
| rs753451796 | 2:37,126,668 | T/C | — | uncertain significance |
| rs937074246 | 2:37,126,691 | T/C | — | uncertain significance |
| rs772208230 | 2:37,126,762 | A/T | — | uncertain significance |
| rs760641469 | 2:37,126,773 | C/T | — | uncertain significance |
| rs1043050578 | 2:37,129,828 | C/G | — | uncertain significance |
| rs752582228 | 2:37,129,884 | C/T | — | uncertain significance |
| rs778874769 | 2:37,132,715 | T/A | — | uncertain significance |
| rs765876629 | 2:37,132,761 | T/C | — | uncertain significance |
| rs7592902 | 2:37,136,036 | A/C | intron variant | — |
| rs7561572 | 2:37,141,336 | A/C | — | — |
| rs2302658 | 2:37,143,140 | A/G | — | benign |
| rs1023851216 | 2:37,143,269 | C/T | — | uncertain significance |
| rs62132551 | 2:37,152,138 | G/A | — | benign |
| rs7583071 | 2:37,152,372 | A/C | — | benign |
| rs17020069 | 2:37,152,425 | T/C | — | benign |
| rs2372785 | 2:37,152,899 | G/T | — | — |
| rs2110994 | 2:37,154,425 | T/A | intron variant | — |
| rs145720518 | 2:37,178,311 | A/C | regulatory region variant | — |
| rs4016036 | 2:37,184,485 | C/G | — | — |
| rs1490652301 | 2:37,193,409 | C/A | — | uncertain significance |
| rs1289571315 | 2:37,193,498 | C/T | — | uncertain significance |
| rs1339119334 | 2:37,193,509 | G/C | — | uncertain significance |
| rs2465862333 | 2:37,193,552 | C/T | — | uncertain significance |
| rs2465862493 | 2:37,193,587 | G/A | — | uncertain significance |
| rs1040781025 | 2:37,193,588 | G/C | — | uncertain significance |
| rs1235595636 | 2:37,193,594 | C/G | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.