RIPOR1
RHO family interacting cell polarization regulator 1
Summary
Enables 14-3-3 protein binding activity. Involved in several processes, including establishment of Golgi localization; negative regulation of Rho guanyl-nucleotide exchange factor activity; and negative regulation of Rho protein signal transduction. Located in several cellular components, including Golgi apparatus; cell leading edge; and cytosol. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants80 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs567068501 | 16:67,572,130 | C/T | — | — |
| rs2507054943 | 16:67,572,329 | A/T | — | uncertain significance |
| rs765902594 | 16:67,572,396 | G/C | — | uncertain significance |
| rs754767058 | 16:67,572,431 | G/A | — | uncertain significance |
| rs968617667 | 16:67,572,435 | G/T | — | uncertain significance |
| rs770755744 | 16:67,572,444 | G/A | — | uncertain significance |
| rs201157660 | 16:67,572,594 | C/T | — | uncertain significance |
| rs200677001 | 16:67,572,604 | C/T | — | uncertain significance |
| rs755576251 | 16:67,572,641 | G/T | — | uncertain significance |
| rs148612121 | 16:67,572,920 | G/A | — | likely benign |
| rs752347460 | 16:67,572,928 | A/G | — | uncertain significance |
| rs9934328 | 16:67,573,367 | G/C | coding sequence variant | — |
| rs1340161896 | 16:67,573,770 | T/C | — | uncertain significance |
| rs371716961 | 16:67,573,992 | C/T | — | uncertain significance |
| rs146876313 | 16:67,573,999 | G/A | — | uncertain significance |
| rs369864235 | 16:67,574,023 | G/A | — | uncertain significance |
| rs201474523 | 16:67,574,044 | C/T | — | uncertain significance |
| rs1222946584 | 16:67,574,053 | G/A | — | uncertain significance |
| rs2507083048 | 16:67,574,064 | G/T | — | uncertain significance |
| rs779391264 | 16:67,574,245 | G/A | — | uncertain significance |
| rs75204333 | 16:67,574,408 | T/C | splice region variant | — |
| rs2507090683 | 16:67,574,513 | A/T | — | uncertain significance |
| rs2507103756 | 16:67,575,454 | T/C | — | uncertain significance |
| rs571690841 | 16:67,575,668 | C/T | — | uncertain significance |
| rs754458713 | 16:67,575,669 | G/A | — | uncertain significance |
| rs201567223 | 16:67,575,782 | C/T | — | uncertain significance |
| rs371602868 | 16:67,575,838 | C/T | — | likely benign |
| rs369179324 | 16:67,575,911 | G/A | — | uncertain significance |
| rs147973168 | 16:67,575,986 | G/A | — | likely benign |
| rs183208454 | 16:67,576,036 | C/T | synonymous variant | — |
| rs141527810 | 16:67,576,104 | G/A | — | uncertain significance |
| rs199574998 | 16:67,576,149 | A/C | — | uncertain significance |
| rs2051011320 | 16:67,576,182 | T/C | — | uncertain significance |
| rs757418472 | 16:67,576,394 | A/C | — | uncertain significance |
| rs1214762599 | 16:67,576,485 | C/T | — | uncertain significance |
| rs767746163 | 16:67,576,500 | C/T | — | uncertain significance |
| rs772692008 | 16:67,576,596 | C/T | — | uncertain significance |
| rs2051032520 | 16:67,576,703 | A/C | — | uncertain significance |
| rs141673634 | 16:67,576,800 | T/C | — | uncertain significance |
| rs147671462 | 16:67,576,872 | G/C | — | uncertain significance |
| rs141407887 | 16:67,576,932 | C/T | — | likely benign |
| rs753758611 | 16:67,576,938 | A/G | — | uncertain significance |
| rs781667886 | 16:67,576,991 | C/T | — | uncertain significance |
| rs541606600 | 16:67,577,004 | T/C | — | uncertain significance |
| rs150376859 | 16:67,577,129 | C/G | — | uncertain significance |
| rs1567576527 | 16:67,577,300 | T/C | — | uncertain significance |
| rs755995770 | 16:67,577,302 | G/A | — | uncertain significance |
| rs559378713 | 16:67,578,302 | C/T | — | uncertain significance |
| rs748651439 | 16:67,578,700 | C/T | — | uncertain significance |
| rs770942148 | 16:67,578,713 | C/T | — | uncertain significance |
| rs137895953 | 16:67,578,880 | G/C | — | uncertain significance |
| rs2507161818 | 16:67,578,913 | C/G | — | uncertain significance |
| rs781312153 | 16:67,578,940 | C/T | — | uncertain significance |
| rs749428939 | 16:67,578,949 | G/A | — | uncertain significance |
| rs751909274 | 16:67,578,984 | C/T | — | uncertain significance |
| rs140035714 | 16:67,578,985 | G/A | — | uncertain significance |
| rs2051131089 | 16:67,579,298 | G/C | — | uncertain significance |
| rs753854878 | 16:67,579,327 | G/C | — | uncertain significance |
| rs1365693319 | 16:67,579,410 | G/A | — | uncertain significance |
| rs375623923 | 16:67,579,578 | C/T | — | uncertain significance |
| rs200327916 | 16:67,579,630 | C/T | — | uncertain significance |
| rs371086414 | 16:67,579,641 | C/T | — | uncertain significance |
| rs746630784 | 16:67,579,642 | G/A | — | uncertain significance |
| rs369188052 | 16:67,579,662 | C/T | — | uncertain significance |
| rs774470272 | 16:67,579,667 | C/T | — | likely benign |
| rs754699420 | 16:67,579,683 | G/A | — | uncertain significance |
| rs752580501 | 16:67,579,687 | A/G | — | uncertain significance |
| rs746241775 | 16:67,579,713 | G/A | — | uncertain significance |
| rs776166140 | 16:67,579,728 | C/T | — | uncertain significance |
| rs751396904 | 16:67,579,859 | T/C | — | uncertain significance |
| rs372790612 | 16:67,579,862 | G/C | — | uncertain significance |
| rs1412971267 | 16:67,579,874 | A/G | — | uncertain significance |
| rs148719338 | 16:67,579,891 | G/A | — | uncertain significance |
| rs142295339 | 16:67,579,903 | G/A | — | uncertain significance |
| rs772232836 | 16:67,579,915 | C/G | — | uncertain significance |
| rs776767210 | 16:67,579,925 | G/A | — | uncertain significance |
| rs140898958 | 16:67,580,113 | C/T | — | uncertain significance |
| rs2051169556 | 16:67,580,293 | G/A | — | uncertain significance |
| rs550633057 | 16:67,580,307 | T/C | — | uncertain significance |
| rs2507187785 | 16:67,580,320 | T/C | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.