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RAPSN

receptor associated protein of the synapse

HCNC Approved Symbol
RAPSN (HGNC:9863)
Genomic Coordinates
11:47,437,764 - 47,449,136 (11p11.2)
Synonyms
RNF205, CMS1D, CMS1E
Disease Associations
This gene is associated with the following 2 diseases in OMIM.
View More Disease Info
Disease NameOMIM IDInheritance
Fetal akinesia deformation sequence 2
618388AR
Myasthenic syndrome, congenital, 11, associated with acetylcholine receptor deficiency
616326AR

Diagnosed Cases

0Patient

There are no patients diagnosed with a variant in the RAPSN gene.

Frequently observed phenotypes

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

No Results