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FYN

FYN proto-oncogene, Src family tyrosine kinase

HCNC Approved Symbol
FYN (HGNC:4037)
Genomic Coordinates
6:111,660,332 - 111,873,452 (6q21)
Synonyms
SYN, SLK, MGC45350
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 are 9 patients* with variant(s) predicted to be damaging.*1 of the patient has been diagnosed with a variant in another gene.