GBP1
guanylate binding protein 1
Summary
Guanylate binding protein expression is induced by interferon. Guanylate binding proteins are characterized by their ability to specifically bind guanine nucleotides (GMP, GDP, and GTP) and are distinguished from the GTP-binding proteins by the presence of 2 binding motifs rather than 3. [provided by RefSeq, Jul 2008]
Known Variants45 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs191833238 | 1:89,517,919 | A/T | downstream gene variant | — |
| rs185838271 | 1:89,518,357 | A/G | 3 prime UTR variant | — |
| rs141247522 | 1:89,519,069 | A/G | — | uncertain significance |
| rs750714490 | 1:89,519,096 | T/G | — | uncertain significance |
| rs111365231 | 1:89,519,903 | T/C | — | — |
| rs146127934 | 1:89,520,400 | T/C | — | likely benign |
| rs199786994 | 1:89,520,420 | T/C | — | uncertain significance |
| rs146959522 | 1:89,520,507 | T/C | — | uncertain significance |
| rs2523471691 | 1:89,520,538 | A/T | — | uncertain significance |
| rs553228904 | 1:89,520,888 | A/G | — | uncertain significance |
| rs1680033975 | 1:89,521,704 | T/C | — | uncertain significance |
| rs574206530 | 1:89,521,758 | C/T | — | likely benign |
| rs1043924679 | 1:89,521,772 | C/T | — | uncertain significance |
| rs763936207 | 1:89,521,773 | C/G | — | uncertain significance |
| rs1680038462 | 1:89,521,838 | A/G | — | uncertain significance |
| rs139042305 | 1:89,521,892 | C/T | — | uncertain significance |
| rs142226400 | 1:89,521,895 | T/C | — | uncertain significance |
| rs746423353 | 1:89,521,900 | T/G | — | likely benign |
| rs147875713 | 1:89,522,538 | G/A | — | uncertain significance |
| rs149073593 | 1:89,522,619 | C/G | — | uncertain significance |
| rs766833210 | 1:89,522,683 | G/C | — | uncertain significance |
| rs1680066896 | 1:89,522,701 | C/A | — | uncertain significance |
| rs745367467 | 1:89,522,784 | G/A | — | uncertain significance |
| rs926385480 | 1:89,522,805 | A/G | — | uncertain significance |
| rs533198085 | 1:89,522,974 | C/T | — | — |
| rs549528891 | 1:89,523,299 | C/A | — | — |
| rs371741027 | 1:89,523,764 | A/G | — | uncertain significance |
| rs144022371 | 1:89,523,802 | C/G | — | uncertain significance |
| rs372549555 | 1:89,523,819 | G/A | — | uncertain significance |
| rs1039835070 | 1:89,524,558 | A/C | — | uncertain significance |
| rs1557749822 | 1:89,524,563 | G/T | — | uncertain significance |
| rs577188089 | 1:89,524,697 | C/T | — | uncertain significance |
| rs147930913 | 1:89,525,049 | C/T | — | uncertain significance |
| rs147085563 | 1:89,525,079 | C/T | — | uncertain significance |
| rs150201512 | 1:89,525,080 | G/A | — | likely benign |
| rs138685353 | 1:89,525,887 | A/G | — | uncertain significance |
| rs146259663 | 1:89,525,900 | C/T | — | uncertain significance |
| rs186011210 | 1:89,525,934 | C/T | — | likely benign |
| rs754228273 | 1:89,528,781 | A/G | — | uncertain significance |
| rs139551612 | 1:89,528,847 | T/A | — | uncertain significance |
| rs149277121 | 1:89,528,850 | G/A | — | likely benign |
| rs2523493170 | 1:89,528,883 | C/T | — | uncertain significance |
| rs149801739 | 1:89,528,887 | T/C | — | likely benign |
| rs148954716 | 1:89,528,898 | A/G | — | uncertain significance |
| rs182786256 | 1:89,530,515 | T/C | regulatory region variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.