CORIN - Gene browser

CORIN

corin, serine peptidase

HCNC Approved Symbol: CORIN (HGNC:19012)
Genomic Coordinates: 4:47,594,001 - 47,838,067 (4p12)
Synonyms: PRSC, CRN, ATC2, Lrp4, TMPRSS10
Disease Associations: This gene is associated with the following 2 diseases in OMIM.

0Patient

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

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

No Results