HSPBP1
HSPA (Hsp70) binding protein 1
Summary
Enables molecular sequestering activity and ubiquitin protein ligase binding activity. Involved in positive regulation of proteasomal ubiquitin-dependent protein catabolic process and positive regulation of protein ubiquitination. Is active in extracellular space. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants31 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs181335004 | 19:55,773,994 | G/C | — | uncertain significance |
| rs199998150 | 19:55,776,753 | C/A | — | likely benign |
| rs758612420 | 19:55,777,324 | G/C | — | uncertain significance |
| rs1568959821 | 19:55,777,339 | A/T | — | uncertain significance |
| rs867800432 | 19:55,777,568 | C/G | — | uncertain significance |
| rs2516275114 | 19:55,777,616 | G/A | — | uncertain significance |
| rs1036541153 | 19:55,777,627 | A/G | — | uncertain significance |
| rs767671307 | 19:55,785,775 | C/A | — | uncertain significance |
| rs2516313202 | 19:55,785,784 | C/T | — | uncertain significance |
| rs766830096 | 19:55,785,790 | C/T | — | uncertain significance |
| rs150486738 | 19:55,785,793 | G/A | — | uncertain significance |
| rs202077081 | 19:55,785,812 | G/A | — | likely benign |
| rs904897256 | 19:55,785,837 | C/T | — | uncertain significance |
| rs780645577 | 19:55,785,880 | C/T | — | uncertain significance |
| rs141743392 | 19:55,785,894 | G/A | — | uncertain significance |
| rs572927428 | 19:55,785,931 | C/T | — | uncertain significance |
| rs754973817 | 19:55,785,951 | C/T | — | uncertain significance |
| rs139452756 | 19:55,785,962 | C/T | — | likely benign |
| rs61733819 | 19:55,789,061 | C/G | — | uncertain significance |
| rs759133962 | 19:55,789,084 | G/A | — | uncertain significance |
| rs773826540 | 19:55,789,174 | C/T | — | uncertain significance |
| rs201699302 | 19:55,789,177 | A/G | — | uncertain significance |
| rs572720723 | 19:55,789,185 | C/T | — | likely benign |
| rs772883558 | 19:55,789,186 | G/A | — | uncertain significance |
| rs201868216 | 19:55,789,212 | C/T | — | likely benign |
| rs7251900 | 19:55,790,282 | T/C | upstream gene variant | — |
| rs145794654 | 19:55,790,845 | G/A | — | benign |
| rs956847727 | 19:55,790,892 | C/T | — | uncertain significance |
| rs1471272724 | 19:55,790,904 | C/A | — | uncertain significance |
| rs536210314 | 19:55,790,915 | C/A | — | uncertain significance |
| rs781337970 | 19:55,790,928 | G/C | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.