| Entry |
|
| Symbol |
DTNA
|
| Name |
|
| Pathway |
| map05412 | Arrhythmogenic right ventricular cardiomyopathy |
|
| Disease |
| H01216 | Left ventricular noncompaction |
| H02791 | Myopathy with myalgia, increased serum creatine kinase, and with or without episodic rhabdomyolysis |
|
| Brite |
KEGG Orthology (KO) [BR:ko00001]
09140 Cellular Processes
09142 Cell motility
04820 Cytoskeleton in muscle cells
K26998 DTNA; dystrobrevin alpha
09160 Human Diseases
09166 Cardiovascular disease
05410 Hypertrophic cardiomyopathy
K26998 DTNA; dystrobrevin alpha
05412 Arrhythmogenic right ventricular cardiomyopathy
K26998 DTNA; dystrobrevin alpha
05414 Dilated cardiomyopathy
K26998 DTNA; dystrobrevin alpha
05416 Viral myocarditis
K26998 DTNA; dystrobrevin alpha
|
| Genes |
» show all
|
| Reference |
|
| Authors |
Sadoulet-Puccio HM, Khurana TS, Cohen JB, Kunkel LM |
| Title |
Cloning and characterization of the human homologue of a dystrophin related phosphoprotein found at the Torpedo electric organ post-synaptic membrane. |
| Journal |
|
| Sequence |
|
| LinkDB |
|