UBAP2L
ubiquitin associated protein 2 like
Summary
Enables RNA binding activity. Involved in binding activity of sperm to zona pellucida; positive regulation of stress granule assembly; and stress granule assembly. Acts upstream of or within hematopoietic stem cell homeostasis. Part of PcG protein complex. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants50 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs188866046 | 1:154,193,425 | C/T | regulatory region variant | — |
| rs545965455 | 1:154,197,628 | C/G | — | uncertain significance |
| rs1296420437 | 1:154,197,630 | C/T | — | uncertain significance |
| rs2526619291 | 1:154,197,687 | C/T | — | pathogenic |
| rs12145394 | 1:154,201,655 | C/T | intron variant | — |
| rs1671024772 | 1:154,207,076 | G/C | — | uncertain significance |
| rs374548186 | 1:154,207,137 | A/G | — | uncertain significance |
| rs199924270 | 1:154,207,163 | C/T | — | uncertain significance |
| rs770656735 | 1:154,207,181 | C/T | — | uncertain significance |
| rs777246805 | 1:154,207,190 | G/C | — | uncertain significance |
| rs2527246387 | 1:154,209,059 | G/T | — | pathogenic |
| rs2527247243 | 1:154,209,088 | G/A | — | pathogenic |
| rs2527279804 | 1:154,209,519 | T/A | — | uncertain significance |
| rs1195580440 | 1:154,209,564 | G/A | — | uncertain significance |
| rs12026615 | 1:154,210,210 | T/C | regulatory region variant | — |
| rs3790613 | 1:154,210,671 | C/A | intron variant | — |
| rs2527559982 | 1:154,215,724 | A/T | — | uncertain significance |
| rs2527704391 | 1:154,218,771 | C/A | — | uncertain significance |
| rs1675470849 | 1:154,218,844 | A/G | — | uncertain significance |
| rs6673752 | 1:154,219,177 | G/A | — | — |
| rs7524346 | 1:154,221,093 | C/T | — | — |
| rs528881045 | 1:154,223,540 | G/T | — | uncertain significance |
| rs76680663 | 1:154,223,633 | A/G | — | uncertain significance |
| rs376270067 | 1:154,223,804 | C/A | — | benign |
| rs2527950204 | 1:154,224,047 | G/A | — | uncertain significance |
| rs375698253 | 1:154,224,083 | G/A | — | uncertain significance |
| rs1252932182 | 1:154,224,109 | C/G | — | uncertain significance |
| rs775257324 | 1:154,226,410 | C/G | — | uncertain significance |
| rs1345081926 | 1:154,226,482 | C/G | — | uncertain significance |
| rs2528067118 | 1:154,226,557 | C/T | — | pathogenic |
| rs140356642 | 1:154,227,643 | C/T | — | uncertain significance |
| rs1469446353 | 1:154,227,709 | C/G | — | uncertain significance |
| rs745463474 | 1:154,227,718 | C/T | — | uncertain significance |
| rs1301319203 | 1:154,227,782 | T/C | — | likely benign |
| rs1395076499 | 1:154,228,191 | C/T | — | uncertain significance |
| rs560099431 | 1:154,229,385 | T/C | — | — |
| rs760270628 | 1:154,229,645 | G/T | — | uncertain significance |
| rs535277118 | 1:154,229,695 | G/C | — | uncertain significance |
| rs376285759 | 1:154,229,716 | T/C | — | uncertain significance |
| rs2528221365 | 1:154,229,900 | A/G | — | uncertain significance |
| rs373722817 | 1:154,231,485 | G/A | — | uncertain significance |
| rs2528412666 | 1:154,233,471 | G/C | — | uncertain significance |
| rs1311304217 | 1:154,233,492 | G/A | — | likely benign |
| rs763832290 | 1:154,233,513 | C/A | — | conflicting classifications of pathogenicity |
| rs36114119 | 1:154,234,121 | G/A | — | benign |
| rs1034044389 | 1:154,234,141 | C/T | — | uncertain significance |
| rs2524687756 | 1:154,239,003 | G/C | — | uncertain significance |
| rs2524790440 | 1:154,241,342 | A/C | — | uncertain significance |
| rs2524793782 | 1:154,241,433 | A/G | — | pathogenic |
| rs1459468103 | 1:154,242,721 | C/T | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.