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SCGN

secretagogin, EF-hand calcium binding protein

HCNC Approved Symbol
SCGN (HGNC:16941)
Genomic Coordinates
6:25,652,215 - 25,701,783 (6p22.2)
Synonyms
SECRET, DJ501N12.8, SEGN, CALBL
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 2 patients* with variant(s) predicted to be damaging.*2 of the patients have been diagnosed with a variant in another gene.

SCGN - Gene browser | 3billion