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Symbol
Name
ID
Chrne
cholinergic receptor, nicotinic, epsilon polypeptide
MGI:87894
Phenotype annotations related to behavior/neurological
Darker colors indicate more annotations
Human Phenotypes
Decreased fetal movement
Feeding difficulties
Feeding difficulties in infancy
Nasal regurgitation
Poor suck
Choking episodes
Weak cry
Dysphonia
Hypernasal speech
Disease(s) Associated with CHRNE
congenital myasthenic syndrome
congenital myasthenic syndrome 4A
congenital myasthenic syndrome 4B
congenital myasthenic syndrome 4C

Mouse Phenotypes
decreased grip strength
weakness
decreased locomotor activity
Availability Mouse Genotype
Chrnetm1Jrs/Chrnetm1Jrs
Chrnetm1Vwi/Chrnetm1Vwi
Tg(Ckm-Chrne*L269F)5Cgz/?

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
04/16/2024
MGI 6.23
The Jackson Laboratory