RCN3
reticulocalbin 3
Summary
Enables calcium ion binding activity. Involved in several processes, including collagen biosynthetic process; positive regulation of peptidase activity; and regulation of phosphatidylinositol 3-kinase/protein kinase B signal transduction. Located in endoplasmic reticulum. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants34 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs150367193 | 19:50,031,814 | C/G | — | uncertain significance |
| rs199527609 | 19:50,031,894 | C/A | — | uncertain significance |
| rs138714642 | 19:50,031,896 | A/G | — | uncertain significance |
| rs756535920 | 19:50,031,937 | C/A | — | uncertain significance |
| rs73582456 | 19:50,034,101 | G/A | downstream gene variant | — |
| rs186451245 | 19:50,034,227 | C/T | downstream gene variant | — |
| rs147804508 | 19:50,035,161 | C/T | intron variant | — |
| rs73582463 | 19:50,037,446 | C/G | splice region variant | — |
| rs960318827 | 19:50,037,508 | G/A | — | uncertain significance |
| rs769564510 | 19:50,037,518 | C/T | — | uncertain significance |
| rs200618256 | 19:50,037,608 | G/C | — | uncertain significance |
| rs745419987 | 19:50,037,616 | G/A | — | uncertain significance |
| rs559607554 | 19:50,038,398 | G/A | — | — |
| rs372578792 | 19:50,040,314 | A/G | — | uncertain significance |
| rs139212536 | 19:50,040,343 | C/T | — | uncertain significance |
| rs141528253 | 19:50,040,348 | C/T | — | likely benign |
| rs773792781 | 19:50,040,352 | C/T | — | uncertain significance |
| rs200804957 | 19:50,040,356 | G/A | — | uncertain significance |
| rs2514122293 | 19:50,040,395 | C/T | — | uncertain significance |
| rs779538986 | 19:50,040,427 | G/A | — | uncertain significance |
| rs926117906 | 19:50,040,446 | G/A | — | uncertain significance |
| rs146820947 | 19:50,042,380 | C/T | — | uncertain significance |
| rs2514133313 | 19:50,045,822 | C/T | — | uncertain significance |
| rs150082451 | 19:50,045,825 | C/A | — | uncertain significance |
| rs970488483 | 19:50,045,887 | C/T | — | uncertain significance |
| rs34459162 | 19:50,045,916 | T/A | missense variant | — |
| rs1326791405 | 19:50,045,923 | G/A | — | uncertain significance |
| rs746696987 | 19:50,045,986 | C/G | — | uncertain significance |
| rs751496757 | 19:50,045,992 | G/A | — | uncertain significance |
| rs781005944 | 19:50,045,998 | G/A | — | uncertain significance |
| rs769222993 | 19:50,046,369 | C/T | — | uncertain significance |
| rs143600694 | 19:50,046,383 | G/A | — | likely benign |
| rs1129459 | 19:50,046,437 | C/A | synonymous variant | — |
| rs773807601 | 19:50,046,454 | A/G | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.