LARP1
La ribonucleoprotein 1, translational regulator
Summary
Enables several functions, including RNA binding activity; eukaryotic initiation factor 4E binding activity; and ribosomal small subunit binding activity. Involved in several processes, including TORC1 signaling; cellular response to rapamycin; and post-transcriptional regulation of gene expression. Located in TORC1 complex and cytoplasmic stress granule. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants39 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs755139217 | 5:154,092,607 | T/G | — | uncertain significance |
| rs117247290 | 5:154,116,556 | G/A | intron variant | — |
| rs56226335 | 5:154,143,755 | A/C | intron variant | — |
| rs78924036 | 5:154,149,065 | G/A | intron variant | — |
| rs1242211984 | 5:154,169,924 | C/G | — | uncertain significance |
| rs2480544124 | 5:154,172,306 | A/T | — | uncertain significance |
| rs144894202 | 5:154,173,176 | C/T | — | uncertain significance |
| rs745924187 | 5:154,173,226 | C/T | — | uncertain significance |
| rs765525971 | 5:154,173,281 | A/G | — | uncertain significance |
| rs766635412 | 5:154,173,386 | G/A | — | likely benign |
| rs770718972 | 5:154,173,392 | C/A | — | uncertain significance |
| rs137864333 | 5:154,173,412 | A/G | — | likely benign |
| rs1403966374 | 5:154,173,459 | C/T | — | uncertain significance |
| rs368771276 | 5:154,173,470 | A/T | — | uncertain significance |
| rs776372021 | 5:154,173,501 | T/C | — | uncertain significance |
| rs770414206 | 5:154,173,509 | C/T | — | uncertain significance |
| rs35598061 | 5:154,173,717 | C/T | — | uncertain significance |
| rs199822685 | 5:154,173,785 | G/T | — | uncertain significance |
| rs556328006 | 5:154,179,235 | A/G | — | uncertain significance |
| rs144624261 | 5:154,179,456 | G/T | — | uncertain significance |
| rs1330941178 | 5:154,179,457 | C/A | — | uncertain significance |
| rs2480637397 | 5:154,181,748 | A/G | — | uncertain significance |
| rs2480637846 | 5:154,181,805 | A/G | — | uncertain significance |
| rs765076218 | 5:154,181,828 | G/C | — | uncertain significance |
| rs1758493050 | 5:154,182,864 | C/A | — | uncertain significance |
| rs774765501 | 5:154,183,138 | C/T | — | uncertain significance |
| rs757929142 | 5:154,185,535 | A/C | — | uncertain significance |
| rs557813643 | 5:154,189,938 | G/C | — | — |
| rs80111507 | 5:154,190,810 | T/C | — | benign |
| rs1328530291 | 5:154,190,815 | T/C | — | uncertain significance |
| rs2480719637 | 5:154,190,874 | T/C | — | uncertain significance |
| rs778895136 | 5:154,191,120 | A/C | — | uncertain significance |
| rs2480744709 | 5:154,193,465 | G/A | — | uncertain significance |
| rs1759493303 | 5:154,193,541 | C/A | — | uncertain significance |
| rs943367823 | 5:154,193,559 | T/A | — | uncertain significance |
| rs2480745954 | 5:154,193,560 | G/T | — | uncertain significance |
| rs2480746089 | 5:154,193,571 | C/A | — | uncertain significance |
| rs2480746213 | 5:154,193,577 | C/T | — | uncertain significance |
| rs753422002 | 5:154,193,643 | C/T | — | conflicting classifications of pathogenicity |
Gene information from NCBI Gene. Variant classifications from ClinVar.