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Symbol
Name
ID
Clcn1
chloride channel, voltage-sensitive 1
MGI:88417
Phenotype annotations related to behavior/neurological
Darker colors indicate more annotations
Human Phenotypes
Myalgia
Disease(s) Associated with CLCN1
Thomsen disease

Mouse Phenotypes
abnormal behavior
decreased exploration in new environment
decreased thigmotaxis
abnormal righting response
impaired righting response
decreased startle reflex
limb grasping
tremors
ataxia
impaired limb coordination
decreased grip strength
abnormal limb posture
abnormal stationary movement
abnormal voluntary movement
abnormal gait
decreased vertical activity
decreased locomotor activity
forelimb paralysis
hindlimb paralysis
paraparesis
abnormal sensory capabilities/reflexes/nociception
Availability Mouse Genotype
Clcn1adr-mto2J/Clcn1adr-mto2J
Clcn1adr-mto5J/Clcn1adr-mto5J
Clcn1adr-mto6J/Clcn1adr-mto6J
Clcn1adr-mto7J/Clcn1adr-mto7J
Clcn1adr-mto8J/Clcn1adr-mto8J
Clcn1adr-mto9J/Clcn1adr-mto9J
Clcn1adr-mto/Clcn1adr-mto
Clcn1adr/Clcn1adr
Clcn1em1(IMPC)Mbp/Clcn1em1(IMPC)Mbp
Clcn1m1Anu/Clcn1m1Anu

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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last database update
04/30/2024
MGI 6.23
The Jackson Laboratory