NKAIN2
sodium/potassium transporting ATPase interacting 2
Summary
This gene encodes a transmembrane protein that interacts with the beta subunit of a sodium/potassium-transporting ATPase. A chromosomal translocation involving this gene is a cause of lymphoma. Alternative splicing results in multiple transcript variants encoding distinct isoforms. [provided by RefSeq, Jul 2014]
Known Variants30 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs911441434 | 6:124,125,358 | A/G | — | uncertain significance |
| rs777170271 | 6:124,125,387 | T/G | — | uncertain significance |
| rs73770293 | 6:124,184,845 | A/C | intron variant | — |
| rs12190776 | 6:124,302,543 | C/T | — | — |
| rs117780815 | 6:124,326,227 | A/T | intron variant | — |
| rs6917824 | 6:124,342,663 | A/G | intron variant | — |
| rs531877822 | 6:124,358,606 | G/T | — | — |
| rs13204086 | 6:124,405,155 | C/T | intron variant | — |
| rs77490164 | 6:124,559,732 | C/T | intron variant | — |
| rs180828775 | 6:124,575,579 | T/A | intron variant | — |
| rs34368457 | 6:124,604,201 | A/G | — | benign |
| rs771269791 | 6:124,604,229 | A/G | — | uncertain significance |
| rs2533396916 | 6:124,604,269 | G/A | — | uncertain significance |
| rs2533397046 | 6:124,604,284 | C/A | — | uncertain significance |
| rs9491140 | 6:124,691,237 | C/T | intron variant | — |
| rs531930 | 6:124,743,507 | A/G | intron variant | — |
| rs577616874 | 6:124,760,516 | T/A | — | — |
| rs117871957 | 6:124,794,202 | T/C | intron variant | — |
| rs530258060 | 6:124,843,366 | T/G | — | — |
| rs191964547 | 6:124,880,246 | G/A | intron variant | — |
| rs497756 | 6:124,897,696 | A/G | — | — |
| rs504008 | 6:124,951,063 | A/T | — | — |
| rs768539349 | 6:124,979,530 | G/A | — | uncertain significance |
| rs538553414 | 6:125,019,217 | C/T | — | — |
| rs71561806 | 6:125,042,505 | G/A | intron variant | — |
| rs28858382 | 6:125,050,993 | C/A | — | — |
| rs9398764 | 6:125,072,022 | A/G | intron variant | — |
| rs182153928 | 6:125,112,522 | G/C | — | uncertain significance |
| rs1477413033 | 6:125,139,544 | G/T | — | uncertain significance |
| rs1229060836 | 6:125,139,624 | T/C | — | likely benign |
Gene information from NCBI Gene. Variant classifications from ClinVar.