Symbol Name ID |
Gsn
gelsolin MGI:95851 |
Darker colors indicate more annotations |
Human Phenotypes | Facial palsy |
Orthostatic hypotension |
Orthostatic hypotension due to autonomic dysfunction |
Bulbar palsy |
Abnormality of the nervous system |
Ataxia |
Dysarthria |
Depression |
Deficit in phonologic short-term memory |
Sleep apnea |
Myokymia |
Bulbar signs |
Constrictive median neuropathy |
Polyneuropathy |
Distal peripheral sensory neuropathy |
Disease(s) Associated with GSN | |||||||||||||||
Finnish type amyloidosis |
Mouse Phenotypes | increased susceptibility to ischemic brain injury |
increased cerebral infarct size |
abnormal nervous system electrophysiology |
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Availability | Mouse Genotype | |||
Gsntm1Djk/Gsntm1Djk |
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 04/23/2024 MGI 6.23 |
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