|
Symbol Name ID |
Nono
non-POU-domain-containing, octamer binding protein MGI:1855692 |
| * | Aspects of the system are reported to show a normal phenotype. |
| Darker colors indicate more annotations |
| Human Phenotypes | Atrial septal defect |
Patent foramen ovale |
Ventricular septal defect |
Abnormal left ventricle morphology |
Left ventricular hypertrophy |
Right ventricular hypertrophy |
Ebstein anomaly of the tricuspid valve |
Left ventricular noncompaction |
Left ventricular noncompaction cardiomyopathy |
Cardiomegaly |
Patent ductus arteriosus |
Abnormal cardiac ventricular function |
Tricuspid regurgitation |
| Disease(s) Associated with NONO | |||||||||||||
| syndromic X-linked intellectual disability 34 |
| Mouse Phenotypes | cardiovascular system phenotype |
decreased heart weight |
small heart |
cardiac interstitial fibrosis |
decreased left ventricle diastolic pressure |
|
| Availability | Mouse Genotype | |||||
| NonoGt(YHA266)Byg/Y | * | |||||
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 04/23/2024 MGI 6.23 |
|
|
|
||
Analysis Tools