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Symbol
Name
ID

Met
met proto-oncogene
MGI:96969

Phenotype annotations related to nervous system

Darker colors indicate more annotations

Human Phenotypes

Spinal cord compression

EEG abnormality

Abnormal nonverbal communicative behavior

Delayed speech and language development

Lack of spontaneous play

Impaired ability to form peer relationships

Autism

Inflexible adherence to routines

Motor stereotypy

Restrictive behavior

Intellectual disability

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 primary somatosensory cortex morphology	abnormal motor neuron innervation pattern	abnormal somatic motor system morphology
Availability	Mouse Genotype	abnormal brain interneuron morphology	abnormal striatum morphology	abnormal orbitofrontal cortex morphology	abnormal primary somatosensory cortex morphology	abnormal motor neuron innervation pattern	abnormal somatic motor system morphology
	Met^tm1Kln/Met^tm1Kln
	Met^tm2Kln/Met^tm2Kln
	Met^tm1Sst/Met^tm1Sst Tg(mI56i-cre,EGFP)1Kc/0 (conditional)

Contributing Projects: 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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