RANBP3L
RAN binding protein 3 like
Summary
Enables SMAD binding activity. Predicted to be involved in several processes, including mesenchymal cell differentiation involved in bone development; negative regulation of osteoblast differentiation; and protein export from nucleus. Predicted to be located in cytoplasm and nucleus. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants32 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs7722251 | 5:36,248,752 | T/G | — | benign |
| rs116800709 | 5:36,249,742 | A/G | 3 prime UTR variant | — |
| rs770112171 | 5:36,249,772 | G/A | — | uncertain significance |
| rs748647142 | 5:36,251,455 | C/G | — | uncertain significance |
| rs2546246492 | 5:36,251,513 | T/C | — | uncertain significance |
| rs2546255171 | 5:36,253,775 | A/G | — | uncertain significance |
| rs771943952 | 5:36,253,783 | A/G | — | uncertain significance |
| rs771032968 | 5:36,253,819 | G/T | — | uncertain significance |
| rs753288741 | 5:36,253,882 | T/C | — | uncertain significance |
| rs193037017 | 5:36,254,499 | A/T | intron variant | — |
| rs567928837 | 5:36,255,329 | A/G | — | — |
| rs1410912410 | 5:36,255,593 | C/T | — | uncertain significance |
| rs893627737 | 5:36,255,601 | G/A | — | uncertain significance |
| rs145127212 | 5:36,255,628 | G/A | — | uncertain significance |
| rs16902871 | 5:36,257,018 | A/G | intron variant | — |
| rs904536484 | 5:36,257,086 | A/G | — | uncertain significance |
| rs760103930 | 5:36,257,101 | C/T | — | uncertain significance |
| rs780587007 | 5:36,257,621 | T/A | — | uncertain significance |
| rs143608109 | 5:36,260,932 | T/C | — | uncertain significance |
| rs2111749444 | 5:36,260,950 | C/T | — | uncertain significance |
| rs376483705 | 5:36,262,068 | T/C | — | uncertain significance |
| rs2546286109 | 5:36,262,087 | C/T | — | uncertain significance |
| rs767069945 | 5:36,262,140 | G/A | — | uncertain significance |
| rs774935712 | 5:36,269,539 | C/T | — | uncertain significance |
| rs2546313219 | 5:36,269,555 | G/A | — | likely benign |
| rs1196281797 | 5:36,271,390 | T/C | — | uncertain significance |
| rs751764442 | 5:36,271,404 | A/G | — | uncertain significance |
| rs199744327 | 5:36,301,440 | G/A | — | uncertain significance |
| rs573322389 | 5:36,301,467 | T/C | — | uncertain significance |
| rs200700462 | 5:36,301,475 | C/T | — | uncertain significance |
| rs779840724 | 5:36,301,479 | C/T | — | uncertain significance |
| rs768607542 | 5:36,301,485 | G/C | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.