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CCN6

cellular communication network factor 6

HCNC Approved Symbol
CCN6 (HGNC:12771)
Genomic Coordinates
6:112,052,813 - 112,069,686 (6q21)
Synonyms
WISP-3, WISP3
Disease Associations
This gene is associated with the following 1 diseases in OMIM.

Diagnosed Cases

8Patients

In total, 8 patients were diagnosed with a variant in the CCN6 gene.

Frequently observed phenotypes

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

Metaphyseal chondrodysplasia
 2 (25.0%)
Skeletal dysplasia
 2 (25.0%)
Ataxia, progressive
 
1 (12.5%)
Difficulty in standing
 
1 (12.5%)
Inability to walk
 
1 (12.5%)
CCN6 - Gene browser | 3billion