| Entrez Gene ID | 4781 |
|---|---|
| Official Gene Symbol | NFIB (GeneCards) |
| Full name | nuclear factor I B |
| Location | 9p23-p22.3 |
| Other ids | Vega : OTTHUMG00000021027 MIM : 600728 HGNC : HGNC:7785 Ensembl : ENSG00000147862 |
| Other names | CTF, NF1-B, NFI-B, NFIB2, NFIB3, NF-I/B, NFI-RED, HMGIC/NFIB |
| Summary | None |
Found 4 variants in this database.
| Variant ID | Entrez Gene ID | Gene | Chromsome | Start | End | Disease | Method |
|---|---|---|---|---|---|---|---|
| 13221 | 4781 | NFIB | 9 | 14440582 | 14440582 | Asymptomatic | HiSeq X Ten |
| 13315 | 4781 | NFIB | 9 | 14473562 | 14473562 | Asymptomatic | HiSeq X Ten |
| 13491 | 4781 | NFIB | 9 | 14541380 | 14541380 | Asymptomatic | HiSeq X Ten |
| 29362 | 4781 | NFIB | 9 | 14307297 | 14307297 | Autism Spectrum Disorders | HiSeq X Ten MiSeq |