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SCFD2

sec1 family domain containing 2

HCNC Approved Symbol
SCFD2 (HGNC:30676)
Genomic Coordinates
: - (4q12)
Synonyms
STXBP1L1, FLJ39514
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.* None of the patients have been diagnosed with a variant in another gene.

SCFD2 - Gene browser | 3billion