Human (56 sources):
Abdominal aortic aneurysm,
Abnormal aortic morphology,
Abnormal left ventricular function,
Abnormal sternum morphology,
Abnormality iris morphology,
Abnormality of connective tissue,
Aortic aneurysm,
Aortic dissection,
Aortic regurgitation,
Aortic root aneurysm,
Arachnodactyly,
Ascending aortic dissection,
Ascending tubular aorta aneurysm,
Bicuspid aortic valve,
Bruising susceptibility,
Cardiomegaly,
Carotid artery dilatation,
Chest pain,
Coronary artery atherosclerosis,
Cryptorchidism,
Cutis marmorata,
Descending aortic dissection,
Descending thoracic aorta aneurysm,
Dilatation of the cerebral artery,
Dural ectasia,
Exertional dyspnea,
Hemoptysis,
High, narrow palate,
Hyperperistalsis,
Hypertelorism,
Hypertension,
Hypovolemia,
Intestinal malrotation,
Ischemic stroke,
Moyamoya phenomenon,
Mucoid extracellular matrix accumulation,
Mydriasis,
Paroxysmal dyspnea,
Patent ductus arteriosus,
Peripheral arterial stenosis,
Periventricular white matter hyperintensities,
Pes planus,
Pneumothorax,
Premature coronary artery atherosclerosis,
Prenatal maternal abnormality,
Pulmonary arterial hypertension,
Retinal infarction,
Retrognathia,
Scoliosis,
Stroke,
Subarachnoid hemorrhage,
Tachypnea,
Tall stature,
Thoracic aortic aneurysm,
Transient ischemic attack,
Vascular dilatation
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Gene expression phenotype annotations where the gene of interest has been
disrupted (manipulated) or is the gene assayed (assayed). Computed annotations are derived from
differential expression analysis from Xenbase processed GEO data with the criteria of a TPM >= 1,
FDR <= 0.05 and an absolute LogFC >= 2.