CCN6 Chromosome 6

Cellular communication network factor 6
67 variants 67 Health Risk

Upload your DNA to see your personal genotypes for variants in CCN6.

What This Gene Does
This gene encodes a member of the WNT1 inducible signaling pathway (WISP) protein subfamily, which belongs to the connective tissue growth factor (CTGF) family. WNT1 is a member of a family of cysteine-rich, glycosylated signaling proteins that mediate diverse developmental processes. The CTGF family members are characterized by four conserved cysteine-rich domains: insulin-like growth factor-binding domain, von Willebrand factor type C module, thrombospondin domain and C-terminal cystine knot-like domain. This gene is overexpressed in colon tumors. It may be downstream in the WNT1 signaling pathway that is relevant to malignant transformation. Mutations of this gene are associated with progressive pseudorheumatoid dysplasia, an autosomal recessive skeletal disorder, indicating that the gene is essential for normal postnatal skeletal growth and cartilage homeostasis. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]
Gene Info
Gene Group
Cellular communication network factors
Locus Type
gene with protein product
Location
6q21
Ensembl
ENSG00000112761
Associated Conditions (4)
Inborn genetic diseases
Progressive pseudorheumatoid dysplasia
CCN6-related disorder
See cases
Key Variants
All Variants (67)
RSID Category Clinical Significance Conditions
RS139375158 Health Risk Conflicting classifications of pathogenicity
RS141505678 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS145590972 Health Risk Conflicting classifications of pathogenicity Progressive pseudorheumatoid dysplasia, Inborn genetic diseases, CCN6-related disorder
RS149609367 Health Risk Conflicting classifications of pathogenicity Progressive pseudorheumatoid dysplasia, Inborn genetic diseases, CCN6-related disorder
RS200472841 Health Risk Conflicting classifications of pathogenicity CCN6-related disorder, CCN6-related disorder
RS34322868 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS375836805 Health Risk Conflicting classifications of pathogenicity Progressive pseudorheumatoid dysplasia, Progressive pseudorheumatoid dysplasia
RS781966767 Health Risk Conflicting classifications of pathogenicity Progressive pseudorheumatoid dysplasia, Progressive pseudorheumatoid dysplasia
RS78266262 Health Risk Conflicting classifications of pathogenicity
RS782703789 Health Risk Conflicting classifications of pathogenicity Progressive pseudorheumatoid dysplasia, CCN6-related disorder, Progressive pseudorheumatoid dysplasia
RS140366226 Health Risk Likely pathogenic
RS1459489540 Health Risk Likely pathogenic
RS1776627236 Health Risk Likely pathogenic Progressive pseudorheumatoid dysplasia, Progressive pseudorheumatoid dysplasia
RS1776631188 Health Risk Likely pathogenic
RS2546929180 Health Risk Likely pathogenic Progressive pseudorheumatoid dysplasia, Progressive pseudorheumatoid dysplasia
RS2546930511 Health Risk Likely pathogenic Progressive pseudorheumatoid dysplasia, Progressive pseudorheumatoid dysplasia
RS1203195727 Health Risk Pathogenic
RS121908900 Health Risk Pathogenic Progressive pseudorheumatoid dysplasia, Progressive pseudorheumatoid dysplasia
RS121908902 Health Risk Pathogenic Progressive pseudorheumatoid dysplasia, Progressive pseudorheumatoid dysplasia
RS121908903 Health Risk Pathogenic Progressive pseudorheumatoid dysplasia, Progressive pseudorheumatoid dysplasia
RS145747429 Health Risk Pathogenic
RS1554311394 Health Risk Pathogenic Progressive pseudorheumatoid dysplasia, Progressive pseudorheumatoid dysplasia
RS1554314738 Health Risk Pathogenic Inborn genetic diseases, Inborn genetic diseases
RS1562599153 Health Risk Pathogenic Progressive pseudorheumatoid dysplasia, Progressive pseudorheumatoid dysplasia
RS1583586843 Health Risk Pathogenic Progressive pseudorheumatoid dysplasia, Progressive pseudorheumatoid dysplasia
RS1776281475 Health Risk Pathogenic
RS1776514016 Health Risk Pathogenic
RS1776635075 Health Risk Pathogenic
RS1776761448 Health Risk Pathogenic
RS1776805400 Health Risk Pathogenic Progressive pseudorheumatoid dysplasia, Progressive pseudorheumatoid dysplasia
RS1776808199 Health Risk Pathogenic
RS2114444927 Health Risk Pathogenic Progressive pseudorheumatoid dysplasia, Progressive pseudorheumatoid dysplasia
RS2114469138 Health Risk Pathogenic Progressive pseudorheumatoid dysplasia, Progressive pseudorheumatoid dysplasia
RS2114473419 Health Risk Pathogenic Progressive pseudorheumatoid dysplasia, Progressive pseudorheumatoid dysplasia
RS2546919756 Health Risk Pathogenic
RS2546919773 Health Risk Pathogenic Progressive pseudorheumatoid dysplasia, Progressive pseudorheumatoid dysplasia
RS2546919941 Health Risk Pathogenic
RS2546924702 Health Risk Pathogenic
RS2546928903 Health Risk Pathogenic CCN6-related disorder, CCN6-related disorder
RS2546928929 Health Risk Pathogenic
RS2546928953 Health Risk Pathogenic
RS2546929120 Health Risk Pathogenic
RS2546929184 Health Risk Pathogenic Progressive pseudorheumatoid dysplasia, Progressive pseudorheumatoid dysplasia
RS375253675 Health Risk Pathogenic
RS781790231 Health Risk Pathogenic Progressive pseudorheumatoid dysplasia, Progressive pseudorheumatoid dysplasia
RS781838640 Health Risk Pathogenic Progressive pseudorheumatoid dysplasia, Progressive pseudorheumatoid dysplasia
RS782172825 Health Risk Pathogenic Progressive pseudorheumatoid dysplasia, Progressive pseudorheumatoid dysplasia
RS782220219 Health Risk Pathogenic
RS782293823 Health Risk Pathogenic
RS782311414 Health Risk Pathogenic
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