DNAJA4
DnaJ heat shock protein family (Hsp40) member A4
Summary
Enables protein-folding chaperone binding activity and unfolded protein binding activity. Involved in several processes, including negative regulation of endothelial cell migration; negative regulation of inclusion body assembly; and protein refolding. Located in cytosol and membrane. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants38 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs77185764 | 15:78,556,076 | G/A | regulatory region variant | — |
| rs78827644 | 15:78,556,250 | G/A | coding sequence variant | — |
| rs79052265 | 15:78,556,258 | A/T | coding sequence variant | — |
| rs12898295 | 15:78,556,589 | C/G | regulatory region variant | — |
| rs2049054145 | 15:78,556,681 | G/C | — | uncertain significance |
| rs117636273 | 15:78,556,895 | G/A | regulatory region variant | — |
| rs578060742 | 15:78,557,092 | C/T | — | likely benign |
| rs373848593 | 15:78,557,099 | A/G | — | likely benign |
| rs148533324 | 15:78,557,163 | G/C | — | uncertain significance |
| rs2505188245 | 15:78,557,189 | G/C | — | uncertain significance |
| rs745848222 | 15:78,557,199 | A/C | — | uncertain significance |
| rs775383535 | 15:78,557,203 | A/G | — | uncertain significance |
| rs1039919708 | 15:78,557,220 | C/G | — | uncertain significance |
| rs147394269 | 15:78,562,911 | G/C | — | uncertain significance |
| rs779468072 | 15:78,562,998 | C/T | — | uncertain significance |
| rs139667760 | 15:78,565,445 | G/A | — | uncertain significance |
| rs377392731 | 15:78,565,460 | T/C | — | uncertain significance |
| rs541645916 | 15:78,565,494 | C/T | — | uncertain significance |
| rs11853189 | 15:78,565,820 | C/T | downstream gene variant | — |
| rs752111684 | 15:78,566,589 | C/T | — | uncertain significance |
| rs145486024 | 15:78,566,642 | C/G | — | uncertain significance |
| rs200583547 | 15:78,566,679 | C/T | — | uncertain significance |
| rs746550055 | 15:78,566,703 | G/A | — | uncertain significance |
| rs574964556 | 15:78,566,722 | A/G | — | uncertain significance |
| rs138390165 | 15:78,566,740 | A/T | — | uncertain significance |
| rs747222954 | 15:78,567,920 | G/A | — | uncertain significance |
| rs2049433004 | 15:78,567,965 | G/T | — | uncertain significance |
| rs776756103 | 15:78,567,990 | A/C | — | uncertain significance |
| rs765263538 | 15:78,568,023 | C/T | — | uncertain significance |
| rs78756785 | 15:78,568,049 | C/G | — | uncertain significance |
| rs9806426 | 15:78,572,359 | C/A | — | — |
| rs150822161 | 15:78,572,477 | T/C | — | uncertain significance |
| rs2505290002 | 15:78,572,625 | G/T | — | uncertain significance |
| rs763055743 | 15:78,572,629 | C/T | — | uncertain significance |
| rs200494161 | 15:78,572,657 | G/C | — | uncertain significance |
| rs370351978 | 15:78,572,739 | C/A | — | uncertain significance |
| rs77568880 | 15:78,572,759 | A/G | — | uncertain significance |
| rs199879308 | 15:78,572,795 | C/T | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.