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FSD2

fibronectin type III and SPRY domain containing 2

HCNC Approved Symbol
FSD2 (HGNC:18024)
Genomic Coordinates
: - (15q25.2)
Synonyms
RP11-127F21, SPRYD1
Disease Associations
Currently, this gene is not associated with any human disease in OMIM.

Diagnosed Cases

There are no diagnosed cases at this time.
However, there is 1 patient* with variant(s) predicted to be damaging.*1 of the patient has been diagnosed with a variant in another gene.

FSD2 - Gene browser | 3billion