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CCIN

calicin

HCNC Approved Symbol
CCIN (HGNC:1568)
Genomic Coordinates
9:36,169,388 - 36,171,334 (9p13.3)
Synonyms
KBTBD14, BTBD20
Disease Associations
This gene is associated with the following 1 diseases in OMIM.

Diagnosed Cases

0Patient

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

Frequently observed phenotypes

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

No Results
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