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CHRM1

cholinergic receptor muscarinic 1

HCNC Approved Symbol
CHRM1 (HGNC:1950)
Genomic Coordinates
11:62,908,679 - 62,921,878 (11q12.3)
Synonyms
Disease Associations
Currently, this gene is not associated with any human disease in OMIM.
However, the following publication(s) suggest a possible gene disease association.
View More Disease Info
ContentsPublications
Muscarinic acetylcholine receptor M1 mutations causing neurodevelopmental disorder and epilepsy.
PMID:34212451

Diagnosed Cases

1Patient

In total, 1 patient was diagnosed with a variant in the CHRM1 gene.

Frequently observed phenotypes

(Top 5 only, Patient count*)
*% of total patients presenting each phenotype is shown in parentheses.

No Results