|
Symbol Name ID |
Hccs
holocytochrome c synthetase MGI:106911 |
| Darker colors indicate more annotations |
| Human Phenotypes | Atrial septal defect |
Ventricular septal defect |
Histiocytoid cardiomyopathy |
Overriding aorta |
Arrhythmia |
Junctional ectopic tachycardia |
| Disease(s) Associated with HCCS | ||||||
| linear skin defects with multiple congenital anomalies 1 |
| Mouse Phenotypes | decreased cardiac muscle glycogen level |
abnormal myocardium layer morphology |
abnormal fetal cardiomyocyte morphology |
abnormal fetal cardiomyocyte mitochondrial morphology |
decreased fetal cardiomyocyte size |
dilated heart atrium |
enlarged heart |
dilated heart left ventricle |
thick ventricular wall |
dilated heart right ventricle |
cardiac interstitial fibrosis |
dilated cardiomyopathy |
abnormal fetal cardiomyocyte proliferation |
decreased fetal cardiomyocyte proliferation |
atrioventricular block |
sinoatrial block |
bundle branch block |
abnormal myocardial fiber physiology |
|
| Availability | Mouse Genotype | ||||||||||||||||||
| Hccstm1Tcc/Hccs+ Nkx2-5tm2(cre)Rph/Nkx2-5+ (conditional) |
|||||||||||||||||||
| Hccstm1Tcc/Hccs+ Nkx2-5tm2(cre)Rph/Nkx2-5+ Tg(CAG-EGFP)D4Nagy/0 Tg(Hmgcr-lacZ)H253Sest/0 (conditional) |
|||||||||||||||||||
| Hccstm1Tcc/Y Nkx2-5tm2(cre)Rph/Nkx2-5+ (conditional) |
|||||||||||||||||||
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO) |
||
|
Citing These Resources Funding Information Warranty Disclaimer, Privacy Notice, Licensing, & Copyright Send questions and comments to User Support. |
last database update 05/28/2024 MGI 6.13 |
|
|
|
||
Analysis Tools