HSF2BP
heat shock transcription factor 2 binding protein
Summary
HSF2 binding protein (HSF2BP) associates with HSF2. The interaction occurs between the trimerization domain of HSF2 and the amino terminal hydrophilic region of HSF2BP that comprises two leucine zipper motifs. HSF2BP may therefore be involved in modulating HSF2 activation. [provided by RefSeq, Jul 2008]
Known Variants33 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs148073623 | 21:44,907,731 | C/G | intergenic variant | — |
| rs150534755 | 21:44,918,007 | G/A | regulatory region variant | — |
| rs86138 | 21:44,932,398 | G/A | intergenic variant | — |
| rs368184709 | 21:44,949,696 | G/A | — | uncertain significance |
| rs145814386 | 21:44,949,728 | C/T | — | uncertain significance |
| rs201950743 | 21:44,949,783 | G/T | — | uncertain significance |
| rs367605171 | 21:44,949,840 | G/C | — | uncertain significance |
| rs11701973 | 21:44,979,671 | G/A | — | — |
| rs547085658 | 21:44,986,066 | C/A | — | — |
| rs144578484 | 21:45,012,161 | C/T | — | likely benign |
| rs12626757 | 21:45,015,698 | T/C | intron variant | — |
| rs532950652 | 21:45,031,242 | T/C | — | — |
| rs755666850 | 21:45,033,781 | G/A | — | uncertain significance |
| rs372621055 | 21:45,033,794 | C/G | — | uncertain significance |
| rs147351989 | 21:45,033,804 | C/T | — | uncertain significance |
| rs1319345920 | 21:45,050,220 | A/G | — | likely pathogenic |
| rs148591527 | 21:45,050,260 | G/T | — | likely benign |
| rs200655253 | 21:45,050,277 | G/A | — | uncertain significance |
| rs200214253 | 21:45,050,305 | C/T | — | uncertain significance |
| rs1051405941 | 21:45,050,329 | C/A | — | uncertain significance |
| rs763884466 | 21:45,050,333 | A/T | — | uncertain significance |
| rs59177757 | 21:45,052,021 | C/A | — | — |
| rs781780538 | 21:45,053,212 | A/G | — | likely pathogenic |
| rs145029179 | 21:45,053,268 | G/A | — | uncertain significance |
| rs551306646 | 21:45,054,592 | A/T | — | — |
| rs8127297 | 21:45,063,847 | G/A | intron variant | — |
| rs200583466 | 21:45,064,200 | G/A | — | likely benign |
| rs745699883 | 21:45,064,210 | C/T | — | uncertain significance |
| rs1405819484 | 21:45,064,270 | A/C | — | uncertain significance |
| rs35110281 | 21:45,068,947 | T/C | — | — |
| rs7279968 | 21:45,077,398 | C/A | — | — |
| rs1183217576 | 21:45,077,971 | C/T | — | uncertain significance |
| rs969060 | 21:45,080,852 | T/C | — | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.