DNAJC16
DnaJ heat shock protein family (Hsp40) member C16
Summary
Involved in regulation of autophagosome size. Located in endoplasmic reticulum membrane. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants49 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs7546668 | 1:15,855,123 | G/C | upstream gene variant | — |
| rs143679565 | 1:15,855,611 | G/C | — | uncertain significance |
| rs994114363 | 1:15,855,626 | C/T | — | uncertain significance |
| rs57551109 | 1:15,859,200 | G/T | — | — |
| rs1179292761 | 1:15,860,768 | C/G | — | uncertain significance |
| rs146586795 | 1:15,862,694 | G/C | — | — |
| rs547950256 | 1:15,862,973 | C/T | — | uncertain significance |
| rs371597930 | 1:15,863,073 | G/A | — | uncertain significance |
| rs2521531171 | 1:15,863,076 | A/G | — | uncertain significance |
| rs142352537 | 1:15,863,160 | A/G | — | uncertain significance |
| rs775593045 | 1:15,863,262 | A/T | — | uncertain significance |
| rs7516435 | 1:15,868,692 | A/G | coding sequence variant | — |
| rs12124078 | 1:15,869,899 | A/G | regulatory region variant | — |
| rs758427393 | 1:15,870,912 | T/C | — | uncertain significance |
| rs1638239227 | 1:15,870,936 | T/A | — | uncertain significance |
| rs370283901 | 1:15,870,941 | C/T | — | uncertain significance |
| rs554936287 | 1:15,870,980 | A/G | — | uncertain significance |
| rs1355551260 | 1:15,871,022 | C/T | — | uncertain significance |
| rs746908478 | 1:15,871,037 | C/T | — | affects |
| rs2521589832 | 1:15,873,266 | C/G | — | uncertain significance |
| rs1329969739 | 1:15,873,307 | G/A | — | uncertain significance |
| rs1638319425 | 1:15,873,358 | T/A | — | uncertain significance |
| rs2521601752 | 1:15,874,786 | G/T | — | uncertain significance |
| rs779303862 | 1:15,874,847 | G/A | — | likely benign |
| rs150485230 | 1:15,874,912 | G/T | — | uncertain significance |
| rs3980014 | 1:15,875,914 | C/G | — | — |
| rs10803392 | 1:15,876,758 | C/A | — | — |
| rs149620751 | 1:15,886,025 | G/A | — | uncertain significance |
| rs767214972 | 1:15,886,032 | G/A | — | uncertain significance |
| rs377391712 | 1:15,886,064 | G/A | — | likely benign |
| rs375931534 | 1:15,886,118 | T/A | — | uncertain significance |
| rs772896520 | 1:15,886,142 | G/A | — | uncertain significance |
| rs1638705772 | 1:15,888,681 | A/C | — | likely benign |
| rs2521682438 | 1:15,888,688 | T/G | — | uncertain significance |
| rs756510307 | 1:15,888,756 | A/G | — | uncertain significance |
| rs144723605 | 1:15,890,424 | G/A | — | uncertain significance |
| rs151124394 | 1:15,890,443 | G/A | — | uncertain significance |
| rs1318438296 | 1:15,890,502 | A/G | — | uncertain significance |
| rs1313169091 | 1:15,892,463 | C/T | — | uncertain significance |
| rs575324634 | 1:15,892,469 | G/A | — | uncertain significance |
| rs149464503 | 1:15,892,481 | G/T | — | uncertain significance |
| rs148700636 | 1:15,892,577 | C/T | — | likely benign |
| rs1435824057 | 1:15,893,611 | G/C | — | uncertain significance |
| rs200177292 | 1:15,893,631 | C/T | — | uncertain significance |
| rs770600583 | 1:15,893,665 | G/A | — | uncertain significance |
| rs762945882 | 1:15,894,302 | G/C | — | uncertain significance |
| rs772987766 | 1:15,894,449 | G/A | — | uncertain significance |
| rs2521720485 | 1:15,894,536 | C/T | — | uncertain significance |
| rs766071537 | 1:15,894,628 | T/C | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.