BSPRY
B-box and SPRY domain containing
Summary
Predicted to enable ubiquitin protein ligase activity. Predicted to be involved in innate immune response. Predicted to act upstream of or within cellular response to leukemia inhibitory factor. Predicted to be located in cell leading edge; membrane; and perinuclear region of cytoplasm. Predicted to be active in cytoplasm. [provided by Alliance of Genome Resources, Apr 2025]
Known Variants42 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs10118275 | 9:116,110,560 | G/C | — | — |
| rs746167046 | 9:116,111,888 | C/T | — | uncertain significance |
| rs2490324251 | 9:116,111,920 | C/T | — | uncertain significance |
| rs957527336 | 9:116,111,931 | A/C | — | uncertain significance |
| rs1276902120 | 9:116,111,945 | T/G | — | uncertain significance |
| rs910133200 | 9:116,112,004 | G/C | — | uncertain significance |
| rs557303447 | 9:116,112,013 | C/T | — | uncertain significance |
| rs2490324781 | 9:116,112,028 | C/T | — | uncertain significance |
| rs746846947 | 9:116,112,032 | G/T | — | uncertain significance |
| rs202215549 | 9:116,116,523 | A/G | — | uncertain significance |
| rs368306479 | 9:116,116,596 | C/T | — | uncertain significance |
| rs747299077 | 9:116,116,599 | G/C | — | uncertain significance |
| rs2490340543 | 9:116,122,788 | G/A | — | uncertain significance |
| rs1192091518 | 9:116,122,843 | T/G | — | uncertain significance |
| rs773758644 | 9:116,122,865 | C/T | — | uncertain significance |
| rs1200488681 | 9:116,122,905 | A/C | — | uncertain significance |
| rs745322208 | 9:116,122,920 | C/T | — | uncertain significance |
| rs200736083 | 9:116,122,967 | C/T | — | uncertain significance |
| rs202046262 | 9:116,130,552 | G/A | — | uncertain significance |
| rs577779388 | 9:116,130,593 | T/C | — | likely benign |
| rs376015885 | 9:116,130,640 | C/T | — | uncertain significance |
| rs776167262 | 9:116,131,910 | C/T | — | uncertain significance |
| rs376745013 | 9:116,131,911 | G/A | — | uncertain significance |
| rs377189582 | 9:116,131,916 | G/A | — | uncertain significance |
| rs372902773 | 9:116,131,923 | G/A | — | uncertain significance |
| rs530360149 | 9:116,131,980 | C/T | — | uncertain significance |
| rs34089316 | 9:116,131,994 | G/C | — | uncertain significance |
| rs748091270 | 9:116,132,034 | A/G | — | uncertain significance |
| rs1178207567 | 9:116,132,106 | A/G | — | uncertain significance |
| rs773924146 | 9:116,132,139 | G/A | — | uncertain significance |
| rs2490356474 | 9:116,132,141 | A/C | — | uncertain significance |
| rs533038118 | 9:116,132,162 | C/T | — | uncertain significance |
| rs202088728 | 9:116,132,198 | C/T | — | uncertain significance |
| rs1254465414 | 9:116,132,202 | A/T | — | uncertain significance |
| rs201963635 | 9:116,132,231 | G/A | — | uncertain significance |
| rs749841740 | 9:116,132,243 | C/A | — | uncertain significance |
| rs199976191 | 9:116,132,277 | G/A | — | uncertain significance |
| rs540060222 | 9:116,132,300 | C/A | — | uncertain significance |
| rs62636612 | 9:116,132,330 | G/A | — | uncertain significance |
| rs967500212 | 9:116,132,339 | C/T | — | uncertain significance |
| rs745872082 | 9:116,132,354 | G/A | — | uncertain significance |
| rs542120882 | 9:116,133,643 | C/T | — | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.