|
Symbol Name ID |
Gns
glucosamine (N-acetyl)-6-sulfatase MGI:1922862 |
| Darker colors indicate more annotations |
| Human Phenotypes | Dysphagia |
Spasticity |
Fatigable weakness of swallowing muscles |
Hydrocephalus |
Ventriculomegaly |
Central nervous system degeneration |
Ataxia |
Vocal cord paresis |
Abnormal pyramidal sign |
Delayed speech and language development |
Dysarthria |
Atypical behavior |
Hypersexuality |
Abnormal temper tantrums |
Aggressive behavior |
Disinhibition |
Hyperactivity |
Hyperorality |
Dementia |
Progressive neurologic deterioration |
Intellectual disability |
Intellectual disability, progressive |
Intellectual disability, severe |
Sleep abnormality |
Obstructive sleep apnea |
Hyperactive deep tendon reflexes |
Gait disturbance |
Loss of ambulation |
Brain imaging abnormality |
Developmental regression |
Motor delay |
Specific learning disability |
Constrictive median neuropathy |
Seizure |
| Disease(s) Associated with GNS | ||||||||||||||||||||||||||||||||||
| mucopolysaccharidosis III |
| Mouse Phenotypes | microgliosis |
astrocytosis |
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| Availability | Mouse Genotype | ||
| Gnstm1e(EUCOMM)Hmgu/Gnstm1e(EUCOMM)Hmgu | |||
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 04/30/2024 MGI 6.23 |
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