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Symbol
Name
ID
Chrng
cholinergic receptor, nicotinic, gamma polypeptide
MGI:87895
Phenotype annotations related to behavior/neurological
*Aspects of the system are reported to show a normal phenotype.
Darker colors indicate more annotations
Human Phenotypes
Decreased fetal movement
Fetal akinesia sequence
Disease(s) Associated with CHRNG
multiple pterygium syndrome

Mouse Phenotypes
behavior/neurological phenotype
abnormal suckling behavior
trunk curl
no spontaneous movement
hindlimb paralysis
Availability Mouse Genotype
Chrngtm1(Chrne)Mknn/Chrngtm1(Chrne)Mknn *
Chrngtm1Mtak/Chrngtm1Mtak
Chrngtm2(Chrne)Vwi/Chrngtm2(Chrne)Vwi

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
11/05/2019
MGI 6.14
The Jackson Laboratory