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EMILIN2

elastin microfibril interfacer 2

HCNC Approved Symbol
EMILIN2 (HGNC:19881)
Genomic Coordinates
18:2,846,232 - 2,916,003 (18p11.32-p11.31)
Synonyms
FLJ33200, FOAP-10
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.

EMILIN2 - Gene browser | 3billion