Symbol Name ID |
Spred1
sprouty protein with EVH-1 domain 1, related sequence MGI:2150016 |
* | Aspects of the system are reported to show a normal phenotype. |
Darker colors indicate more annotations |
Human Phenotypes | Vestibular schwannoma |
Neurofibroma |
Chiari type I malformation |
Delayed speech and language development |
Atypical behavior |
Hyperactivity |
Attention deficit hyperactivity disorder |
Cognitive impairment |
Short attention span |
Dystonia |
Brain imaging abnormality |
Motor delay |
Specific learning disability |
Seizure |
Disease(s) Associated with SPRED1 | ||||||||||||||
Legius syndrome |
Mouse Phenotypes | nervous system phenotype |
abnormal brain morphology |
hydrocephaly |
abnormal excitatory postsynaptic potential |
reduced long-term potentiation |
absent long-term depression |
enhanced paired-pulse facilitation |
|
Availability | Mouse Genotype | |||||||
Spred1em1(IMPC)Ccpcz/Spred1em1(IMPC)Ccpcz | ||||||||
Spred1tm1Hiin/Spred1tm1Hiin | * |
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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