NALF1
NALCN channel auxiliary factor 1
Summary
Predicted to contribute to stretch-activated, monoatomic cation-selective, calcium channel activity. Predicted to be involved in calcium ion import across plasma membrane. Located in plasma membrane. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants36 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs141380144 | 13:107,822,917 | T/C | — | likely benign |
| rs1296387496 | 13:107,822,936 | G/C | — | uncertain significance |
| rs748293538 | 13:107,822,994 | T/C | — | uncertain significance |
| rs774707777 | 13:107,823,029 | G/T | — | uncertain significance |
| rs145827476 | 13:107,823,044 | A/T | — | uncertain significance |
| rs1878784183 | 13:107,823,065 | T/C | — | uncertain significance |
| rs372642834 | 13:107,863,028 | T/C | — | uncertain significance |
| rs16969868 | 13:107,871,712 | G/A | — | — |
| rs9520344 | 13:107,902,770 | T/C | — | — |
| rs76725696 | 13:107,996,834 | C/T | intron variant | — |
| rs1830756 | 13:108,080,223 | C/A | regulatory region variant | — |
| rs9520462 | 13:108,134,909 | A/C | intron variant | — |
| rs181144204 | 13:108,150,508 | A/G | intron variant | — |
| rs11619828 | 13:108,218,865 | C/T | intron variant | — |
| rs957788 | 13:108,257,220 | T/C | intron variant | — |
| rs117202665 | 13:108,429,826 | T/C | intron variant | — |
| rs2036707 | 13:108,484,454 | G/A | intron variant | — |
| rs1509091 | 13:108,491,592 | C/G | — | — |
| rs2501868891 | 13:108,518,077 | A/C | — | uncertain significance |
| rs760962812 | 13:108,518,307 | G/A | — | uncertain significance |
| rs202196215 | 13:108,518,346 | G/A | — | uncertain significance |
| rs777667377 | 13:108,518,349 | G/A | — | likely benign |
| rs2501484933 | 13:108,518,362 | A/G | — | uncertain significance |
| rs942729245 | 13:108,518,412 | G/A | — | uncertain significance |
| rs544196360 | 13:108,518,452 | C/G | — | uncertain significance |
| rs201168561 | 13:108,518,527 | C/T | — | uncertain significance |
| rs1167417705 | 13:108,518,535 | T/G | — | uncertain significance |
| rs2501486126 | 13:108,518,557 | T/G | — | uncertain significance |
| rs199609587 | 13:108,518,565 | G/A | — | uncertain significance |
| rs548984312 | 13:108,518,572 | C/T | — | uncertain significance |
| rs1234546217 | 13:108,518,581 | G/A | — | uncertain significance |
| rs931273903 | 13:108,518,604 | G/C | — | uncertain significance |
| rs2501487843 | 13:108,518,807 | C/G | — | uncertain significance |
| rs139771382 | 13:108,518,809 | A/C | — | uncertain significance |
| rs145281946 | 13:108,518,859 | A/C | — | uncertain significance |
| rs776603795 | 13:108,518,873 | C/G | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.