GBP6
guanylate binding protein family member 6
Summary
Guanylate-binding proteins, such as GBP6, are induced by interferon and hydrolyze GTP to both GDP and GMP (Olszewski et al., 2006 [PubMed 16689661]).[supplied by OMIM, Dec 2008]
Known Variants42 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs181573277 | 1:89,831,179 | C/T | regulatory region variant | — |
| rs763809484 | 1:89,834,121 | G/T | — | uncertain significance |
| rs116429247 | 1:89,834,141 | G/A | — | likely benign |
| rs148123280 | 1:89,834,182 | C/A | — | uncertain significance |
| rs774052556 | 1:89,834,241 | T/C | — | uncertain significance |
| rs139938902 | 1:89,834,253 | G/A | — | uncertain significance |
| rs773035311 | 1:89,835,165 | C/T | — | uncertain significance |
| rs1329000986 | 1:89,835,192 | T/C | — | uncertain significance |
| rs2524140186 | 1:89,843,687 | T/C | — | uncertain significance |
| rs2524140316 | 1:89,843,725 | T/C | — | uncertain significance |
| rs373092127 | 1:89,843,984 | C/T | — | uncertain significance |
| rs139135600 | 1:89,843,996 | A/G | — | uncertain significance |
| rs139547805 | 1:89,844,062 | T/G | — | uncertain significance |
| rs1184408695 | 1:89,844,162 | G/C | — | uncertain significance |
| rs749611563 | 1:89,845,956 | A/G | — | uncertain significance |
| rs150239430 | 1:89,845,972 | A/G | — | uncertain significance |
| rs113658121 | 1:89,845,985 | G/A | — | benign |
| rs1652940628 | 1:89,846,029 | A/T | — | uncertain significance |
| rs199555552 | 1:89,846,031 | C/T | — | uncertain significance |
| rs116333431 | 1:89,846,080 | A/G | — | uncertain significance |
| rs368045971 | 1:89,846,095 | C/G | — | uncertain significance |
| rs976021477 | 1:89,846,097 | A/C | — | uncertain significance |
| rs149793418 | 1:89,847,286 | C/T | — | uncertain significance |
| rs116475216 | 1:89,847,531 | A/G | — | likely benign |
| rs531273768 | 1:89,848,247 | G/T | — | uncertain significance |
| rs1040099680 | 1:89,848,255 | G/C | — | uncertain significance |
| rs2524156523 | 1:89,848,274 | T/C | — | uncertain significance |
| rs113532469 | 1:89,848,352 | G/T | — | benign |
| rs1157185182 | 1:89,848,394 | A/T | — | uncertain significance |
| rs149263534 | 1:89,848,434 | A/G | — | uncertain significance |
| rs116173091 | 1:89,849,256 | G/C | — | uncertain significance |
| rs2524159272 | 1:89,849,284 | C/A | — | uncertain significance |
| rs928655 | 1:89,849,574 | G/C | — | — |
| rs775406848 | 1:89,849,777 | G/A | — | uncertain significance |
| rs753064086 | 1:89,849,821 | T/G | — | uncertain significance |
| rs1415872105 | 1:89,850,822 | A/G | — | uncertain significance |
| rs76159539 | 1:89,850,843 | G/A | — | benign |
| rs2524164542 | 1:89,850,877 | C/T | — | uncertain significance |
| rs2524164587 | 1:89,850,885 | A/C | — | uncertain significance |
| rs1305512307 | 1:89,850,920 | C/A | — | uncertain significance |
| rs148760203 | 1:89,850,927 | G/A | — | uncertain significance |
| rs142400726 | 1:89,850,930 | G/A | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.