aga Phenotypes

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Phenotypes

Gene Literature (21)

Nucleotides (74)

Interactants (98)

XB-GENEPAGE-1001621

Gene Symbol: aga Gene Name: aspartylglucosaminidase

Monarch Ortholog Phenotypes These phenotypes are associated with this gene with a has phenotype relation via Monarch.
Human (74 sources): Abnormal cortical bone morphology, Abnormal facial shape, Abnormal vertebral morphology, Abnormality of amino acid metabolism, Abnormality of metabolism/homeostasis, Abnormality of the dentition, Abnormality of the ulna, Acne, Angiokeratoma corporis diffusum, Anterior beaking of lumbar vertebrae, Anteverted nares, Arthritis, Aspartylglucosaminuria, Beaking of vertebral bodies, Behavioral abnormality, Brachycephaly, Broad face, Carious teeth, Cataract, Cerebral atrophy, Chronic otitis media, Coarse facial features, Decreased prothrombin time, Delayed skeletal maturation, Delayed speech and language development, Depressed nasal bridge, Developmental regression, Diarrhea, Dyskinesia, Dysostosis multiplex, Generalized hypotonia, Gingival overgrowth, Hepatomegaly, Hernia, Hoarse voice, Hypertelorism, Hypoplastic frontal sinuses, Hypotonia, Intellectual disability, Joint stiffness, Kyphosis, Large face, Macroglossia, Macroorchidism, Malabsorption, Mandibular prognathia, Microcephaly, Microtia, Mitral regurgitation, Neurological speech impairment, Neutropenia, Pathologic fracture, Pectus carinatum, Pes planus, Platyspondyly, Recurrent respiratory infections, Scoliosis, Seizure, Short nose, Short stature, Sleep disturbance, Spasticity, Splenomegaly, Spondylolisthesis, Spondylolysis, Thick lower lip vermilion, Thick vermilion border, Thickened calvaria, Umbilical hernia, Vacuolated lymphocytes, Vascular skin abnormality, Wide mouth, Wide nasal bridge, obsolete Joint laxity [+]
Mouse (16 sources): Purkinje cell degeneration, abnormal axon morphology, abnormal brain ventricle morphology, abnormal cerebral hemisphere morphology, abnormal lysosome morphology, abnormal renal glomerulus morphology, abnormal spatial learning, abnormal urinary bladder urothelium morphology, behavior/neurological phenotype, colorless urine, disheveled coat, impaired balance, impaired limb coordination, multifocal hepatic necrosis, premature death, short stride length [+]
View all ortholog results at Monarch