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Symbol Name ID |
Nfatc1
nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1 MGI:102469 |
| Darker colors indicate more annotations |
| Human Phenotypes | Atrial septal defect |
Ventricular septal defect |
Perimembranous ventricular septal defect |
Atrioventricular canal defect |
Tetralogy of Fallot |
Pulmonary artery stenosis |
Patent ductus arteriosus |
Pulmonic stenosis |
| Disease(s) Associated with NFATC1 | ||||||||
| ventricular septal defect |
| Mouse Phenotypes | abnormal cardiac outflow tract development |
decreased atrioventricular cushion size |
abnormal mitral valve development |
abnormal tricuspid valve development |
abnormal semilunar valve development |
abnormal heart morphology |
abnormal mitral valve cusp morphology |
abnormal tricuspid valve cusp morphology |
abnormal interventricular septum morphology |
ventricular septal defect |
cardiac hypertrophy |
abnormal semilunar valve morphology |
absent aortic valve cusps |
absent pulmonary valve cusps |
pericardial effusion |
abnormal cardiovascular system physiology |
abnormal blood circulation |
gastrointestinal hemorrhage |
semilunar valve regurgitation |
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| Availability | Mouse Genotype | |||||||||||||||||||
| Nfatc1tm1Glm/Nfatc1tm1Glm | ||||||||||||||||||||
| Nfatc1tm1Mak/Nfatc1tm1Mak | ||||||||||||||||||||
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO) |
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last database update 03/24/2026 MGI 6.24 |
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