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Symbol
Name
ID
Lmna
lamin A
MGI:96794
Phenotype annotations related to cardiovascular system
Darker colors indicate more annotations
Human Phenotypes
Intracranial hemorrhage
Ventricular hypertrophy
Abnormal aortic valve morphology
Aortic valve calcification
Abnormal mitral valve morphology
Mitral valve calcification
Abnormal myocardium morphology
Cardiomyopathy
Dilated cardiomyopathy
Hypertrophic cardiomyopathy
Interstitial cardiac fibrosis
Pericardial effusion
Pulmonary artery stenosis
Carotid artery occlusion
Coronary artery atherosclerosis
Premature coronary artery atherosclerosis
Atherosclerosis
Precocious atherosclerosis
Premature arteriosclerosis
Prominent superficial veins
Abnormal cerebral vascular morphology
Stroke
Transient ischemic attack
Abnormal left ventricular function
Reduced left ventricular ejection fraction
Left ventricular diastolic dysfunction
Left ventricular systolic dysfunction
Aortic regurgitation
Aortic valve stenosis
Mitral regurgitation
Mitral stenosis
Hypertension
Raynaud phenomenon
Pulmonary arterial hypertension
Arrhythmia
Sinoatrial block
Sinus bradycardia
Sudden cardiac death
Supraventricular arrhythmia
Atrial fibrillation
Paroxysmal atrial fibrillation
Atrial flutter
Supraventricular tachycardia
Paroxysmal atrial tachycardia
Ventricular tachycardia
Ventricular arrhythmia
Ventricular escape rhythm
Cardiac conduction abnormality
Atrioventricular block
First degree atrioventricular block
Second degree atrioventricular block
Third degree atrioventricular block
Heart block
Left anterior fascicular block
Myocardial infarction
Angina pectoris
Congestive heart failure
Syncope
Splenomegaly
Prominent superficial blood vessels
Telangiectasia of the skin
Disease(s) Associated with LMNA
autosomal dominant Emery-Dreifuss muscular dystrophy 2
autosomal recessive Emery-Dreifuss muscular dystrophy 3
congenital muscular dystrophy due to LMNA mutation
dilated cardiomyopathy 1A
dilated cardiomyopathy-hypergonadotropic hypogonadism syndrome
Emery-Dreifuss muscular dystrophy
familial partial lipodystrophy type 2
progeria
Werner syndrome

Mouse Phenotypes
abnormal artery morphology
abnormal aorta tunica adventitia morphology
abnormal aorta smooth muscle morphology
increased aorta wall thickness
calcified aortic arch
calcified thoracic aorta
calcified aorta
atherosclerotic lesions
decreased vascular endothelial cell number
decreased capillary density
abnormal physiological neovascularization
vascular smooth muscle hypoplasia
abnormal myocardial fiber morphology
decreased myocardial fiber number
decreased myocardial fiber size
myocardial fiber degeneration
myocardium necrosis
thin myocardium
cardiac muscle degeneration
abnormal heart development
abnormal heart morphology
increased heart atrium size
dilated heart atrium
decreased heart weight
enlarged heart
cardiac hypertrophy
small heart
abnormal heart left ventricle morphology
decreased heart left ventricle weight
dilated heart left ventricle
dilated heart right ventricle
cardiac fibrosis
cardiac interstitial fibrosis
dilated cardiomyopathy
decreased cardiac output
decreased cardiac muscle contractility
decreased ventricle muscle contractility
abnormal heart echocardiography feature
decreased heart rate
prolonged RR interval
abnormal impulse conducting system conduction
prolonged PR interval
prolonged P wave
prolonged QRS complex duration
sinoatrial block
pulmonary hypertension
abnormal vascular smooth muscle physiology
abnormal vasodilation
congestive heart failure
Availability Mouse Genotype
LmnaGt(S7-1F1)Sor/LmnaGt(S7-1F1)Sor
Lmnatm1.1Bliu/Lmnatm1.1Bliu
Lmnatm1.1Otin/Lmnatm1.1Otin
Lmnatm1Gbon/Lmnatm1Gbon
Lmnatm2.1Gbon/Lmnatm2.1Gbon
Lmnatm2Stw/Lmnatm2Stw
Lmnatm3Stw/Lmnatm3Stw
Lmnatm5Lgf/Lmnatm5Lgf
Lmnatm8Lgf/Lmnatm8Lgf
Lmnatm12Lgf/Lmnatm12Lgf
Lmnatm1.1Bliu/Lmna+
Lmnatm1.1Otin/Lmna+
Lmnatm2.1Gbon/Lmna+
Lmnatm1Bliu/Lmna+
Tg(Tek-cre)1Ywa/0  (conditional)

Contributing Projects:
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
05/14/2024
MGI 6.23
The Jackson Laboratory