ATG13
autophagy related 13
Summary
The protein encoded by this gene is an autophagy factor and a target of the TOR kinase signaling pathway. The encoded protein is essential for autophagosome formation and mitophagy. [provided by RefSeq, Oct 2016]
Known Variants31 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs139834704 | 11:46,647,343 | G/A | intron variant | — |
| rs560718432 | 11:46,660,911 | G/C | — | — |
| rs757216241 | 11:46,665,882 | A/G | — | uncertain significance |
| rs750851624 | 11:46,665,905 | C/G | — | uncertain significance |
| rs143855756 | 11:46,666,948 | T/A | — | benign |
| rs746417694 | 11:46,666,950 | C/T | — | uncertain significance |
| rs145889337 | 11:46,671,756 | C/T | — | uncertain significance |
| rs10769204 | 11:46,676,357 | C/T | intron variant | — |
| rs561781278 | 11:46,677,810 | T/A | — | uncertain significance |
| rs1323674318 | 11:46,678,669 | C/T | — | uncertain significance |
| rs1318363954 | 11:46,678,696 | C/G | — | uncertain significance |
| rs780215956 | 11:46,679,130 | G/A | — | uncertain significance |
| rs773910954 | 11:46,679,166 | A/G | — | uncertain significance |
| rs201108289 | 11:46,681,012 | T/C | — | uncertain significance |
| rs979644222 | 11:46,681,015 | T/C | — | uncertain significance |
| rs1380542124 | 11:46,685,622 | G/A | — | uncertain significance |
| rs1352787233 | 11:46,686,408 | T/G | — | uncertain significance |
| rs774788651 | 11:46,686,441 | G/T | — | uncertain significance |
| rs1342796611 | 11:46,686,490 | A/G | — | uncertain significance |
| rs140270738 | 11:46,689,352 | G/A | — | uncertain significance |
| rs61736849 | 11:46,689,353 | T/C | — | benign |
| rs147787573 | 11:46,689,363 | G/A | — | uncertain significance |
| rs757516956 | 11:46,690,082 | A/T | — | uncertain significance |
| rs746488204 | 11:46,690,097 | A/G | — | uncertain significance |
| rs2502277306 | 11:46,690,386 | G/A | — | uncertain significance |
| rs138756347 | 11:46,690,408 | C/T | — | uncertain significance |
| rs778665063 | 11:46,690,435 | A/G | — | uncertain significance |
| rs760250544 | 11:46,690,981 | C/T | — | uncertain significance |
| rs769891260 | 11:46,691,009 | G/A | — | uncertain significance |
| rs193920809 | 11:46,693,804 | G/C | — | uncertain significance |
| rs148029215 | 11:46,693,860 | C/A | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.