gaa Phenotypes

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Phenotypes

Gene Literature (17)

Nucleotides (57)

Interactants (100)

XB-GENEPAGE-6054130

Gene Symbol: gaa Gene Name: alpha glucosidase

Monarch Ortholog Phenotypes These phenotypes are associated with this gene with a has phenotype relation via Monarch.
Human (39 sources): Abdominal wall muscle weakness, Abnormal CNS myelination, Abnormality of metabolism/homeostasis, Abnormality of the cardiovascular system, Areflexia, Arrhythmia, Atrioventricular block, Cardiomegaly, Cognitive impairment, Diaphragmatic paralysis, Dilatation of the cerebral artery, Dysphagia, Dysphasia, Dyspnea, EEG abnormality, EMG abnormality, Elevated circulating creatine kinase concentration, Emphysema, Fever, Firm muscles, Gait disturbance, Generalized hypotonia, Generalized muscle weakness, Hearing impairment, Hepatomegaly, Hypertrophic cardiomyopathy, Hypotonia, Macroglossia, Muscle weakness, Myopathy, Proximal muscle weakness, Recurrent respiratory infections, Respiratory insufficiency, Respiratory insufficiency due to muscle weakness, Seizure, Shortened PR interval, Splenomegaly, Type II diabetes mellitus, Wolff-Parkinson-White syndrome [+]
Mouse (20 sources): abnormal QRS complex, abnormal Z line morphology, abnormal glycogen homeostasis, abnormal heart shape, abnormal impulse conducting system conduction, abnormal lysosome morphology, abnormal muscle fiber morphology, abnormal myocardial fiber morphology, abnormal sarcomere morphology, decreased grip strength, decreased locomotor activity, decreased skeletal muscle mass, decreased vertical activity, dilated heart left ventricle, hindlimb paralysis, increased body mass index, increased brain glycogen level, increased cardiac muscle glycogen level, increased skeletal muscle glycogen level, muscular atrophy [+]
View all ortholog results at Monarch