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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.
View More Disease Info
Disease NameOMIM IDInheritance
?Cardiomyopathy, familial hypertrophic, 30, atrial
620734AR
Preeclampsia/eclampsia 5
614595-

Diagnosed Cases

0Patient

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

Frequently observed phenotypes

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

No Results