EMILIN1 - Gene browser

EMILIN1

elastin microfibril interfacer 1

HCNC Approved Symbol: EMILIN1 (HGNC:19880)
Genomic Coordinates: 2:27,078,615 - 27,086,403 (2p23.3)
Synonyms: DKFZp586M121, gp115, EMILIN
Disease Associations: This gene is associated with the following 1 diseases in OMIM.

0Patient

There are no patients diagnosed with a variant in the EMILIN1 gene.

(Top 5 only, Patient count*)
*% of total patients presenting each phenotype is shown in parentheses.

No Results