NANOGNB
NANOG neighbor homeobox
Summary
Predicted to enable DNA-binding transcription factor activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants13 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs117994500 | 12:7,917,779 | T/C | upstream gene variant | — |
| rs1344595825 | 12:7,917,918 | G/A | — | uncertain significance |
| rs1264965838 | 12:7,917,924 | T/C | — | uncertain significance |
| rs1266206139 | 12:7,917,928 | A/G | — | uncertain significance |
| rs1394528557 | 12:7,917,949 | G/A | — | uncertain significance |
| rs150173189 | 12:7,919,259 | C/G | intron variant | — |
| rs1306356071 | 12:7,922,616 | A/T | — | uncertain significance |
| rs1470218122 | 12:7,922,789 | G/A | — | likely benign |
| rs893631836 | 12:7,922,859 | C/T | — | uncertain significance |
| rs1301512948 | 12:7,922,895 | A/G | — | likely benign |
| rs1865283235 | 12:7,923,063 | A/G | — | uncertain significance |
| rs548793247 | 12:7,923,071 | A/G | — | uncertain significance |
| rs562302947 | 12:7,923,285 | C/T | — | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.