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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 neuron mitochondrial morphology |
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 04/30/2024 MGI 6.23 |
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