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Symbol
Name
ID
Chrnd
cholinergic receptor, nicotinic, delta polypeptide
MGI:87893
Phenotype annotations related to nervous system
Darker colors indicate more annotations
Human Phenotypes
Microcephaly
Facial palsy
Dysphagia
Easy fatigability
Akinesia
Inability to walk
Disease(s) Associated with CHRND
congenital myasthenic syndrome 3A
congenital myasthenic syndrome 3B
congenital myasthenic syndrome 3C
multiple pterygium syndrome

Mouse Phenotypes
abnormal action potential
abnormal PNS synaptic transmission
abnormal endplate potential
abnormal miniature endplate potential
Availability Mouse Genotype
Tg(Ckm-Chrnd*S262T)40Cgz/0

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
03/03/2020
MGI 6.15
The Jackson Laboratory