| Entrez Gene ID | 9324 |
|---|---|
| Official Gene Symbol | HMGN3 (GeneCards) |
| Full name | high mobility group nucleosomal binding domain 3 |
| Location | 6q14.1 |
| Other ids | Vega : OTTHUMG00000015073 MIM : 604502 HGNC : HGNC:12312 Ensembl : ENSG00000118418 |
| Other names | TRIP7, PNAS-24, PNAS-25 |
| Summary | The protein encoded by this gene binds thyroid hormone receptor beta in the presence of thyroid hormone. The encoded protein, a member of the HMGN protein family, is thought to reduce the compactness of the chromatin fiber in nucleosomes, thereby enhancing transcription from chromatin templates. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. There is a related pseudogene on chromosome 1. [provided by RefSeq, Jan 2016] |
Found 1 variant in this database.
| Variant ID | Entrez Gene ID | Gene | Chromsome | Start | End | Disease | Method |
|---|---|---|---|---|---|---|---|
| 10144 | 9324 | HMGN3 | 6 | 79910398 | 79910398 | Cockayne syndrome | HiSeq X Ten |