Symbol Name ID |
Dvl1
dishevelled segment polarity protein 1 MGI:94941 |
* | Aspects of the system are reported to show a normal phenotype. |
Darker colors indicate more annotations |
Human Phenotypes | Microcephaly |
Hemiparesis |
Delayed speech and language development |
Schizophrenia |
Bipolar affective disorder |
Attention deficit hyperactivity disorder |
Intellectual disability |
Global developmental delay |
Specific learning disability |
Seizure |
Disease(s) Associated with DVL1 | ||||||||||
DiGeorge syndrome | ||||||||||
Disease(s) Associated with DVL1P1 | ||||||||||
DiGeorge syndrome |
Mouse Phenotypes | nervous system phenotype |
reduced sensorimotor gating |
decreased prepulse inhibition |
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Availability | Mouse Genotype | |||
Dvl1tm1Awb/Dvl1tm1Awb | * |
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 07/05/2024 MGI 6.24 |
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