Symbol Name ID |
Met
met proto-oncogene MGI:96969 |
Darker colors indicate more annotations |
Human Phenotypes | Spinal cord compression |
EEG abnormality |
Inflexible adherence to routines |
Delayed speech and language development |
Abnormal nonverbal communicative behavior |
Lack of spontaneous play |
Impaired ability to form peer relationships |
Autism |
Motor stereotypy |
Restrictive behavior |
Intellectual disability |
Peripheral neuropathy |
Constrictive median neuropathy |
Seizure |
Paresthesia |
Disease(s) Associated with MET | |||||||||||||||
autistic disorder | |||||||||||||||
multiple myeloma |
Mouse Phenotypes | abnormal brain interneuron morphology |
abnormal striatum morphology |
abnormal orbitofrontal cortex morphology |
abnormal cerebral cortex morphology |
abnormal primary somatosensory cortex morphology |
abnormal motor neuron innervation pattern |
abnormal somatic motor system morphology |
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Availability | Mouse Genotype | |||||||
Mettm1Kln/Mettm1Kln | ||||||||
Mettm2Kln/Mettm2Kln | ||||||||
Mettm1Sst/Mettm1Sst Tg(mI56i-cre,EGFP)1Kc/0 (conditional) |
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Mettm1Sst/Mettm1Sst Tg(Nes-cre)1Kln/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 09/03/2024 MGI 6.24 |
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