TESC
tescalcin
Summary
Enables calcium ion binding activity. Involved in several processes, including positive regulation of macromolecule biosynthetic process; positive regulation of myeloid cell differentiation; and positive regulation of sodium:proton antiporter activity. Located in several cellular components, including cytosol; lamellipodium; and nucleoplasm. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants30 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs201444090 | 12:117,476,974 | G/A | — | benign |
| rs376205330 | 12:117,476,980 | G/A | — | benign |
| rs58470318 | 12:117,478,979 | G/C | — | — |
| rs59756806 | 12:117,479,019 | T/C | intron variant | — |
| rs6490104 | 12:117,483,843 | A/G | regulatory region variant | — |
| rs116635547 | 12:117,484,381 | C/T | — | benign |
| rs979965735 | 12:117,484,388 | C/T | — | likely benign |
| rs76346744 | 12:117,484,436 | G/A | — | benign |
| rs1160446471 | 12:117,484,451 | C/T | — | likely benign |
| rs2500321920 | 12:117,484,601 | G/A | — | uncertain significance |
| rs979997799 | 12:117,484,608 | G/A | — | uncertain significance |
| rs777799568 | 12:117,484,612 | G/A | — | likely benign |
| rs531621385 | 12:117,484,617 | T/C | — | uncertain significance |
| rs113474183 | 12:117,484,652 | G/T | — | benign |
| rs189129803 | 12:117,486,876 | G/A | — | benign |
| rs753875219 | 12:117,486,892 | T/A | — | uncertain significance |
| rs148314787 | 12:117,486,924 | G/C | — | uncertain significance |
| rs373277209 | 12:117,486,930 | A/C | — | uncertain significance |
| rs7968761 | 12:117,487,432 | G/A | intron variant | — |
| rs7972416 | 12:117,491,824 | A/G | intron variant | — |
| rs11837022 | 12:117,492,256 | G/C | — | — |
| rs368043922 | 12:117,494,625 | G/A | — | likely benign |
| rs1489436586 | 12:117,494,659 | T/A | — | uncertain significance |
| rs7964668 | 12:117,498,825 | C/A | — | — |
| rs758078242 | 12:117,513,128 | C/T | — | uncertain significance |
| rs562957217 | 12:117,513,139 | G/A | — | uncertain significance |
| rs1282630843 | 12:117,519,507 | G/T | — | — |
| rs73405293 | 12:117,522,917 | G/A | intron variant | — |
| rs1402687997 | 12:117,537,071 | G/A | — | uncertain significance |
| rs1447697894 | 12:117,537,072 | A/G | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.