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FSCN2

fascin actin-bundling protein 2, retinal

HCNC Approved Symbol
FSCN2 (HGNC:3960)
Genomic Coordinates
17:81,515,062 - 81,537,130 (17q25.3)
Synonyms
RP30, RFSN
Disease Associations
This gene is associated with the following 1 diseases in OMIM.
View More Disease Info
Disease NameOMIM IDInheritance
Retinitis pigmentosa 30
607921-

Diagnosed Cases

1Patient

In total, 1 patient was diagnosed with a variant in the FSCN2 gene.

Frequently observed phenotypes

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

No Results