Symbol Name ID |
Chst3
carbohydrate sulfotransferase 3 MGI:1858224 |
* | Aspects of the system are reported to show a normal phenotype. |
Darker colors indicate more annotations |
Human Phenotypes | Intellectual disability |
Waddling gait |
Delayed gross motor development |
Disease(s) Associated with CHST3 | |||
spondyloepiphyseal dysplasia with congenital joint dislocations |
Mouse Phenotypes | nervous system phenotype |
decreased prepulse inhibition |
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Availability | Mouse Genotype | ||
Chst3tm1Dgen/Chst3tm1Dgen | |||
Chst3tm1Tmu/Chst3tm1Tmu | * |
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 05/14/2024 MGI 6.23 |
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