| Entrez Gene ID | 93649 |
|---|---|
| Official Gene Symbol | MYOCD (GeneCards) |
| Full name | myocardin |
| Location | 17p12 |
| Other ids | Vega : OTTHUMG00000058767 MIM : 606127 HGNC : HGNC:16067 Ensembl : ENSG00000141052 |
| Other names | MYCD |
| Summary | This gene encodes a nuclear protein, which is expressed in heart, aorta, and in smooth muscle cell-containing tissues. It functions as a transcriptional co-activator of serum response factor (SRF) and modulates expression of cardiac and smooth muscle-specific SRF-target genes, and thus may play a crucial role in cardiogenesis and differentiation of the smooth muscle cell lineage. Alternatively spliced transcript variants encoding different isoforms have been found for this gene.[provided by RefSeq, Sep 2009] |
Found 3 variants in this database.
| Variant ID | Entrez Gene ID | Gene | Chromsome | Start | End | Disease | Method |
|---|---|---|---|---|---|---|---|
| 19794 | 93649 | MYOCD | 17 | 12636078 | 12636078 | Asymptomatic | HiSeq X Ten |
| 28306 | 93649 | MYOCD | 17 | 12641505 | 12641505 | Asymptomatic | HiSeq X Ten Single cell Sequencing Cell cloning |
| 29593 | 93649 | MYOCD | 17 | 12620732 | 12620732 | Autism Spectrum Disorders | HiSeq X Ten Single cell Sequencing Cell cloning MiSeq |