Symbol Name ID |
Mapk1
mitogen-activated protein kinase 1 MGI:1346858 |
* | Aspects of the system are reported to show a normal phenotype. |
Darker colors indicate more annotations |
Human Phenotypes | Microcephaly |
Cavum septum pellucidum |
Delayed speech and language development |
Anxiety |
Aggressive behavior |
Attention deficit hyperactivity disorder |
Head-banging |
Intellectual disability |
Global developmental delay |
Generalized-onset seizure |
Infantile spasms |
Disease(s) Associated with MAPK1 | |||||||||||
Noonan syndrome 13 |
Mouse Phenotypes | nervous system phenotype |
abnormal neuron differentiation |
abnormal cerebral cortex morphology |
thin cerebral cortex |
astrocytosis |
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Availability | Mouse Genotype | |||||
Mapk1tm1Kuta/Mapk1tm1Kuta | * | |||||
Mapk1tm1.2Kuta/Mapk1tm1.2Kuta Tg(Nes-cre)1Kag/0 (conditional) |
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Mapk1tm1Gela/Mapk1tm1Gela Tg(GFAP-cre)25Mes/0 (conditional) |
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 08/02/2024 MGI 6.24 |
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