PATL1
PAT1 homolog 1, processing body mRNA decay factor
Summary
Enables poly(G) binding activity and poly(U) RNA binding activity. Involved in P-body assembly and deadenylation-dependent decapping of nuclear-transcribed mRNA. Located in CCR4-NOT complex; P-body; and cytosol. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants38 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs1332685778 | 11:59,406,554 | C/T | — | likely benign |
| rs374318871 | 11:59,406,633 | G/A | — | uncertain significance |
| rs2495383160 | 11:59,410,451 | T/A | — | uncertain significance |
| rs759712162 | 11:59,415,270 | G/A | — | uncertain significance |
| rs1205677053 | 11:59,415,283 | G/A | — | uncertain significance |
| rs909542968 | 11:59,416,989 | T/C | — | uncertain significance |
| rs1055473802 | 11:59,417,029 | G/T | — | uncertain significance |
| rs371738317 | 11:59,417,039 | A/G | — | likely benign |
| rs1861412545 | 11:59,417,079 | T/C | — | uncertain significance |
| rs1226240307 | 11:59,418,237 | A/G | — | uncertain significance |
| rs763444872 | 11:59,418,264 | C/T | — | uncertain significance |
| rs374236615 | 11:59,419,943 | T/C | — | uncertain significance |
| rs758221100 | 11:59,420,020 | T/G | — | uncertain significance |
| rs368269303 | 11:59,420,029 | G/A | — | uncertain significance |
| rs373449614 | 11:59,420,447 | C/T | — | uncertain significance |
| rs533446752 | 11:59,420,448 | G/A | — | uncertain significance |
| rs114449363 | 11:59,421,509 | G/A | — | benign |
| rs189267978 | 11:59,421,532 | T/C | — | likely benign |
| rs113191943 | 11:59,421,556 | C/T | intron variant | — |
| rs372063665 | 11:59,423,054 | C/T | — | uncertain significance |
| rs77539250 | 11:59,423,117 | G/T | — | benign |
| rs183877144 | 11:59,423,150 | G/A | — | likely benign |
| rs2495069013 | 11:59,423,185 | T/G | — | uncertain significance |
| rs1357989262 | 11:59,423,457 | T/G | — | uncertain significance |
| rs777289577 | 11:59,423,473 | C/G | — | uncertain significance |
| rs2495070399 | 11:59,423,482 | C/T | — | uncertain significance |
| rs1379861234 | 11:59,423,988 | T/G | — | uncertain significance |
| rs200304211 | 11:59,424,020 | A/G | — | benign |
| rs61901655 | 11:59,425,023 | C/T | — | uncertain significance |
| rs2495075314 | 11:59,425,053 | G/C | — | uncertain significance |
| rs558116138 | 11:59,425,083 | T/C | — | likely benign |
| rs368281531 | 11:59,425,154 | C/G | — | uncertain significance |
| rs1276322425 | 11:59,426,353 | G/A | — | uncertain significance |
| rs116027464 | 11:59,426,365 | G/T | — | benign |
| rs371253037 | 11:59,426,419 | G/T | — | uncertain significance |
| rs767139662 | 11:59,426,790 | C/T | — | uncertain significance |
| rs372793509 | 11:59,426,850 | C/T | — | uncertain significance |
| rs745662061 | 11:59,434,428 | C/T | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.