Symbol Name ID |
Hgsnat
heparan-alpha-glucosaminide N-acetyltransferase MGI:1196297 |
Darker colors indicate more annotations |
Human Phenotypes | Dysphagia |
Loss of speech |
Hyperactivity |
Motor deterioration |
Intellectual disability |
Sleep abnormality |
Global developmental delay |
Motor delay |
Seizure |
Disease(s) Associated with HGSNAT | |||||||||
mucopolysaccharidosis type IIIC |
Mouse Phenotypes | abnormal Purkinje cell mitochondrial morphology |
microgliosis |
abnormal nervous system morphology |
abnormal cerebral cortex morphology |
abnormal Purkinje cell morphology |
abnormal CNS glial cell morphology |
astrocytosis |
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Availability | Mouse Genotype | |||||||
Hgsnattm1a(EUCOMM)Wtsi/Hgsnattm1a(EUCOMM)Wtsi |
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 08/02/2024 MGI 6.24 |
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