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Symbol
Name
ID

Aga
aspartylglucosaminidase
MGI:104873

Phenotype annotations related to nervous system

Darker colors indicate more annotations

Human Phenotypes	Microcephaly	Spasticity	Cerebral atrophy	Delayed speech and language development	Intellectual disability	Developmental regression	Seizure
Disease(s) Associated with AGA
aspartylglucosaminuria

Mouse Phenotypes		abnormal brain ventricle morphology	enlarged brain ventricles	abnormal cerebral hemisphere morphology	abnormal cerebellum morphology	Purkinje cell degeneration	astrocytosis	neurogenic bladder	abnormal axon morphology	neurodegeneration
Availability	Mouse Genotype	abnormal brain ventricle morphology	enlarged brain ventricles	abnormal cerebral hemisphere morphology	abnormal cerebellum morphology	Purkinje cell degeneration	astrocytosis	neurogenic bladder	abnormal axon morphology	neurodegeneration
	Aga^tm1Pltn/Aga^tm1Pltn
	Aga^tm1Vk/Aga^tm1Vk

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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