GBP7
guanylate binding protein 7
Summary
Guanylate-binding proteins, such as GBP7, are induced by interferon and hydrolyze GTP to both GDP and GMP (Olszewski et al., 2006 [PubMed 16689661]).[supplied by OMIM, Dec 2008]
Known Variants46 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs187586392 | 1:89,597,872 | C/T | — | uncertain significance |
| rs143239867 | 1:89,597,881 | C/G | — | uncertain significance |
| rs764858765 | 1:89,597,954 | C/T | — | uncertain significance |
| rs752396686 | 1:89,597,964 | C/G | — | uncertain significance |
| rs758158653 | 1:89,597,965 | T/G | — | uncertain significance |
| rs374167387 | 1:89,599,002 | A/G | — | uncertain significance |
| rs202078573 | 1:89,599,030 | C/T | — | uncertain significance |
| rs377097410 | 1:89,599,120 | T/C | — | uncertain significance |
| rs144793011 | 1:89,599,228 | C/G | intron variant | — |
| rs144796129 | 1:89,605,830 | T/C | intron variant | — |
| rs114675739 | 1:89,607,009 | A/G | intron variant | — |
| rs755436006 | 1:89,607,258 | G/T | — | uncertain significance |
| rs115159884 | 1:89,610,252 | T/C | intron variant | — |
| rs2523660739 | 1:89,613,267 | G/A | — | uncertain significance |
| rs186580098 | 1:89,613,326 | C/A | — | uncertain significance |
| rs2523661733 | 1:89,613,438 | C/A | — | uncertain significance |
| rs2523661764 | 1:89,613,454 | C/A | — | likely benign |
| rs749396805 | 1:89,614,981 | C/A | — | uncertain significance |
| rs542953952 | 1:89,615,030 | A/T | — | uncertain significance |
| rs767570581 | 1:89,615,036 | A/G | — | uncertain significance |
| rs560981037 | 1:89,615,064 | C/T | — | uncertain significance |
| rs759654598 | 1:89,615,177 | A/G | — | likely benign |
| rs1682144668 | 1:89,615,231 | T/C | — | uncertain significance |
| rs1298609727 | 1:89,616,147 | A/G | — | uncertain significance |
| rs138811948 | 1:89,616,389 | C/A | upstream gene variant | — |
| rs140430191 | 1:89,618,022 | A/G | — | uncertain significance |
| rs1682222314 | 1:89,618,031 | T/C | — | uncertain significance |
| rs374864805 | 1:89,618,038 | C/T | — | uncertain significance |
| rs765200010 | 1:89,618,111 | T/A | — | uncertain significance |
| rs1006879983 | 1:89,618,429 | G/A | — | uncertain significance |
| rs140471146 | 1:89,618,432 | A/T | — | uncertain significance |
| rs182057240 | 1:89,618,503 | T/C | upstream gene variant | — |
| rs184513274 | 1:89,622,132 | C/T | intron variant | — |
| rs148463853 | 1:89,625,578 | T/G | intron variant | — |
| rs1440391225 | 1:89,630,434 | C/G | — | uncertain significance |
| rs748026424 | 1:89,630,439 | G/A | — | uncertain significance |
| rs369178248 | 1:89,630,461 | G/A | — | uncertain significance |
| rs1010784550 | 1:89,630,493 | A/C | — | uncertain significance |
| rs115610787 | 1:89,636,014 | G/A | intron variant | — |
| rs375911963 | 1:89,637,432 | T/G | — | uncertain significance |
| rs144350186 | 1:89,637,457 | T/C | — | likely benign |
| rs1398370708 | 1:89,637,464 | G/A | — | uncertain significance |
| rs148758371 | 1:89,637,476 | C/T | — | uncertain significance |
| rs761006533 | 1:89,637,480 | A/G | — | uncertain significance |
| rs564360281 | 1:89,637,519 | T/C | — | uncertain significance |
| rs150059676 | 1:89,641,198 | T/C | intron variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.