RETREG3
reticulophagy regulator family member 3
Summary
Predicted to enable endoplasmic reticulum-autophagosome adaptor activity. Involved in endoplasmic reticulum tubular network organization; positive regulation of neuron projection development; and reticulophagy. Located in endoplasmic reticulum tubular network. Part of protein-containing complex. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants35 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs575678530 | 17:40,733,835 | T/C | — | uncertain significance |
| rs147763292 | 17:40,733,907 | G/C | — | uncertain significance |
| rs776110979 | 17:40,733,931 | G/A | — | uncertain significance |
| rs371218425 | 17:40,733,937 | C/T | — | uncertain significance |
| rs764542549 | 17:40,733,938 | G/A | — | uncertain significance |
| rs965082838 | 17:40,733,946 | C/G | — | uncertain significance |
| rs1460374082 | 17:40,733,991 | G/A | — | uncertain significance |
| rs149072183 | 17:40,733,994 | G/A | — | uncertain significance |
| rs141316520 | 17:40,734,106 | C/T | — | uncertain significance |
| rs138787430 | 17:40,734,132 | G/C | — | uncertain significance |
| rs141966783 | 17:40,734,156 | C/T | — | uncertain significance |
| rs2510716709 | 17:40,734,166 | A/C | — | uncertain significance |
| rs758899525 | 17:40,734,208 | C/T | — | uncertain significance |
| rs1567920142 | 17:40,734,211 | C/G | — | uncertain significance |
| rs746880289 | 17:40,734,798 | T/A | — | uncertain significance |
| rs770627957 | 17:40,734,800 | C/T | — | uncertain significance |
| rs551348476 | 17:40,735,559 | T/C | — | uncertain significance |
| rs371460668 | 17:40,735,586 | G/A | — | uncertain significance |
| rs1190178899 | 17:40,735,595 | C/T | — | uncertain significance |
| rs144875771 | 17:40,737,178 | C/T | — | uncertain significance |
| rs147958787 | 17:40,737,197 | G/A | — | uncertain significance |
| rs765024458 | 17:40,738,101 | C/T | — | likely benign |
| rs768495003 | 17:40,738,860 | G/C | — | uncertain significance |
| rs2093124228 | 17:40,739,860 | G/T | — | uncertain significance |
| rs12951632 | 17:40,741,013 | T/C | intron variant | — |
| rs1327444902 | 17:40,744,090 | G/C | — | uncertain significance |
| rs774835274 | 17:40,744,157 | C/T | — | uncertain significance |
| rs112666141 | 17:40,753,714 | G/A | intron variant | — |
| rs751445516 | 17:40,761,233 | G/A | — | uncertain significance |
| rs570020009 | 17:40,761,260 | G/A | — | uncertain significance |
| rs762373592 | 17:40,761,282 | C/T | — | uncertain significance |
| rs757889076 | 17:40,761,320 | G/A | — | uncertain significance |
| rs142711318 | 17:40,761,324 | C/G | — | uncertain significance |
| rs200120312 | 17:40,761,330 | C/G | — | uncertain significance |
| rs748920342 | 17:40,761,338 | G/C | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.