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Symbol
Name
ID
Chrm1
cholinergic receptor, muscarinic 1, CNS
MGI:88396
Phenotype annotations related to nervous system
*Aspects of the system are reported to show a normal phenotype.
Darker colors indicate more annotations
Human Phenotypes
Facial palsy
Dysphagia
Fatigable weakness
Dysarthria
Disease(s) Associated with CHRM1
myasthenia gravis

Mouse Phenotypes
nervous system phenotype
abnormal auditory cortex morphology
abnormal auditory cortex tonotopy
abnormal CNS synapse formation
abnormal nervous system electrophysiology
abnormal excitatory postsynaptic currents
abnormal excitatory postsynaptic potential
abnormal inhibitory postsynaptic currents
abnormal miniature excitatory postsynaptic currents
abnormal long-term depression
reduced long-term depression
decreased paired-pulse facilitation
Availability Mouse Genotype
Chrm1tm1Jwe/Chrm1tm1Jwe *
Chrm1tm1Kano/Chrm1tm1Kano
Chrm1tm1Nmn/Chrm1tm1Nmn
Chrm1tm1Stl/Chrm1tm1Stl
Chrm1tm2.1Stl/Chrm1tm2.1Stl
Emx1tm1.1(cre)Ito/0  (conditional)
Chrm1tm2.1Stl/Chrm1tm2.1Stl
Tg(Grik4-cre)G32-4Stl/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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last database update
05/28/2024
MGI 6.13
The Jackson Laboratory