Symbol Name ID |
Ndst1
N-deacetylase/N-sulfotransferase (heparan glucosaminyl) 1 MGI:104719 |
Darker colors indicate more annotations |
Human Phenotypes | Ventriculomegaly |
Ataxia |
Delayed speech and language development |
Poor speech |
Aggressive behavior |
Agitation |
Self-injurious behavior |
Intellectual disability |
Sleep abnormality |
Global developmental delay |
Delayed fine motor development |
Delayed gross motor development |
Seizure |
Disease(s) Associated with NDST1 | |||||||||||||
autosomal recessive intellectual developmental disorder 46 |
Mouse Phenotypes | pituitary gland hypoplasia |
abnormal brain development |
abnormal forebrain development |
abnormal brain commissure morphology |
abnormal hippocampal commissure morphology |
abnormal anterior commissure morphology |
abnormal diencephalon morphology |
abnormal telencephalon morphology |
absent olfactory bulb |
abnormal CNS glial cell morphology |
anencephaly |
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Availability | Mouse Genotype | |||||||||||
Ndst1b2b2230Clo/Ndst1b2b2230Clo | ||||||||||||
Ndst1tm1.1Grob/Ndst1tm1.1Grob |
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 05/21/2024 MGI 6.23 |
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