| Entrez Gene ID | 4821 |
|---|---|
| Official Gene Symbol | NKX2-2 (GeneCards) |
| Full name | NK2 homeobox 2 |
| Location | 20p11.22 |
| Other ids | Vega : OTTHUMG00000170524 MIM : 604612 HGNC : HGNC:7835 Ensembl : ENSG00000125820 |
| Other names | NKX2B, NKX2.2 |
| Summary | The protein encoded by this gene contains a homeobox domain and may be involved in the morphogenesis of the central nervous system. This gene is found on chromosome 20 near NKX2-4, and these two genes appear to be duplicated on chromosome 14 in the form of TITF1 and NKX2-8. The encoded protein is likely to be a nuclear transcription factor. [provided by RefSeq, Jul 2008] |
Found 2 variants in this database.
| Variant ID | Entrez Gene ID | Gene | Chromsome | Start | End | Disease | Method |
|---|---|---|---|---|---|---|---|
| 1467 | 4821 | NKX2-2 | 20 | 21494134 | 21494134 | Autism Spectrum Disorders | NextSeq500 v2 |
| 29524 | 4821 | NKX2-2 | 20 | 21494134 | 21494134 | Autism Spectrum Disorders | NextSeq500 v2 MiSeq |