RTKN2
rhotekin 2
Summary
Involved in negative regulation of intrinsic apoptotic signaling pathway; positive regulation of NF-kappaB transcription factor activity; and positive regulation of non-canonical NF-kappaB signal transduction. Located in cytoplasm and nucleus. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants37 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs148375207 | 10:63,957,705 | T/C | — | uncertain significance |
| rs2492186765 | 10:63,957,714 | T/C | — | uncertain significance |
| rs771777243 | 10:63,957,755 | T/C | — | likely benign |
| rs1349806695 | 10:63,957,821 | G/A | — | uncertain significance |
| rs571337539 | 10:63,957,825 | C/T | — | uncertain significance |
| rs1038595439 | 10:63,957,840 | G/C | — | uncertain significance |
| rs145577789 | 10:63,957,852 | T/C | — | uncertain significance |
| rs200719773 | 10:63,957,903 | T/C | — | uncertain significance |
| rs139538566 | 10:63,958,001 | C/T | — | uncertain significance |
| rs3125734 | 10:63,958,112 | T/G | missense variant | — |
| rs1564498631 | 10:63,959,537 | C/T | — | uncertain significance |
| rs1315432782 | 10:63,959,605 | C/T | — | uncertain significance |
| rs35576264 | 10:63,959,929 | C/T | intron variant | — |
| rs34390319 | 10:63,960,611 | T/C | intron variant | — |
| rs878870027 | 10:63,964,693 | G/T | — | uncertain significance |
| rs1349099175 | 10:63,964,702 | T/C | — | uncertain significance |
| rs151060040 | 10:63,964,703 | G/C | — | uncertain significance |
| rs769678425 | 10:63,964,759 | T/C | — | uncertain significance |
| rs1302597762 | 10:63,976,925 | C/A | — | uncertain significance |
| rs77837774 | 10:63,976,948 | G/A | — | uncertain significance |
| rs557898940 | 10:63,977,004 | A/G | — | uncertain significance |
| rs1181304946 | 10:63,978,024 | A/G | — | uncertain significance |
| rs148771454 | 10:63,983,020 | T/C | — | uncertain significance |
| rs141182251 | 10:63,983,047 | T/C | — | uncertain significance |
| rs1009697242 | 10:63,983,086 | A/T | — | uncertain significance |
| rs202199799 | 10:63,983,090 | C/G | — | uncertain significance |
| rs2492361815 | 10:63,995,837 | C/T | — | uncertain significance |
| rs2492362620 | 10:63,995,906 | C/T | — | uncertain significance |
| rs145539217 | 10:63,995,951 | G/A | — | uncertain significance |
| rs1417297024 | 10:63,995,985 | C/G | — | uncertain significance |
| rs151279740 | 10:63,995,991 | C/T | — | uncertain significance |
| rs537556691 | 10:64,001,070 | G/A | — | — |
| rs767076096 | 10:64,022,399 | T/C | — | uncertain significance |
| rs1842796800 | 10:64,022,496 | C/A | — | uncertain significance |
| rs1314861536 | 10:64,022,550 | C/T | — | uncertain significance |
| rs1001087753 | 10:64,028,321 | G/C | — | uncertain significance |
| rs769223693 | 10:64,028,327 | C/A | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.