CCDC88C Chromosome 14

Coiled-coil and HOOK domain protein 88C
126 variants 126 Health Risk

Upload your DNA to see your personal genotypes for variants in CCDC88C.

What This Gene Does
This gene encodes a ubiquitously expressed coiled-coil domain-containing protein that interacts with the dishevelled protein and is a negative regulator of the Wnt signalling pathway. The protein encoded by this gene has a PDZ-domain binding motif in its C-terminus with which it interacts with the dishevelled protein. Dishevelled is a scaffold protein involved in the regulation of the Wnt signaling pathway. The Wnt signaling pathway plays an important role in embryonic development, tissue maintenance, and cancer progression. Mutations in this gene cause autosomal recessive, primary non-syndromic congenital hydrocephalus; a condition characterized by excessive accumulation of cerebrospinal fluid in the ventricles of the brain. [provided by RefSeq, Jan 2013]
Gene Info
Gene Group
HOOK related protein family
Locus Type
gene with protein product
Location
14q32.11-q32.12
Ensembl
ENSG00000015133
Associated Conditions (19)
Inborn genetic diseases
Hydrocephalus
nonsyndromic
autosomal recessive 1
Spinocerebellar ataxia type 40
CCDC88C-related disorder
Intellectual disability
Epilepsy
Clear cell carcinoma of kidney
Colorectal cancer
Lung cancer
Cervical cancer
Familial cancer of breast
Uveal melanoma
Thyroid cancer
nonmedullary
1
Spastic ataxia
Congenital hydrocephalus
Key Variants
All Variants (126)
RSID Category Clinical Significance Conditions
RS115510695 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS1285918522 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS1366859752 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS1396400378 Health Risk Conflicting classifications of pathogenicity Hydrocephalus, nonsyndromic, autosomal recessive 1
RS142295786 Health Risk Conflicting classifications of pathogenicity Spinocerebellar ataxia type 40, Hydrocephalus, Inborn genetic diseases
RS142539336 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, CCDC88C-related disorder, Intellectual disability
RS1440642205 Health Risk Conflicting classifications of pathogenicity Hydrocephalus, nonsyndromic, autosomal recessive 1
RS151228192 Health Risk Conflicting classifications of pathogenicity CCDC88C-related disorder, CCDC88C-related disorder
RS1555413299 Health Risk Conflicting classifications of pathogenicity
RS183312399 Health Risk Conflicting classifications of pathogenicity Hydrocephalus, nonsyndromic, autosomal recessive 1
RS183319966 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS185401166 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS185802741 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS187949234 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, CCDC88C-related disorder, Inborn genetic diseases
RS199730476 Health Risk Conflicting classifications of pathogenicity
RS199967225 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS200079946 Health Risk Conflicting classifications of pathogenicity CCDC88C-related disorder, CCDC88C-related disorder
RS200081065 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS200244690 Health Risk Conflicting classifications of pathogenicity CCDC88C-related disorder, Intellectual disability, CCDC88C-related disorder
RS200488874 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, CCDC88C-related disorder, Inborn genetic diseases
RS200543687 Health Risk Conflicting classifications of pathogenicity CCDC88C-related disorder, CCDC88C-related disorder
RS200650758 Health Risk Conflicting classifications of pathogenicity Hydrocephalus, nonsyndromic, autosomal recessive 1
RS200769097 Health Risk Conflicting classifications of pathogenicity Spinocerebellar ataxia type 40, Hydrocephalus, nonsyndromic
RS201044013 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Clear cell carcinoma of kidney, Colorectal cancer
RS201193446 Health Risk Conflicting classifications of pathogenicity
RS201259963 Health Risk Conflicting classifications of pathogenicity
RS201414940 Health Risk Conflicting classifications of pathogenicity Hydrocephalus, nonsyndromic, autosomal recessive 1
RS201675394 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, CCDC88C-related disorder, Inborn genetic diseases
RS201931182 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS369069440 Health Risk Conflicting classifications of pathogenicity Hydrocephalus, nonsyndromic, autosomal recessive 1
RS374858033 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS375400399 Health Risk Conflicting classifications of pathogenicity
RS3950029 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, CCDC88C-related disorder, Inborn genetic diseases
RS560507685 Health Risk Conflicting classifications of pathogenicity
RS574962577 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Spinocerebellar ataxia type 40, Hydrocephalus
RS575390201 Health Risk Conflicting classifications of pathogenicity
RS575697663 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS61743881 Health Risk Conflicting classifications of pathogenicity CCDC88C-related disorder, CCDC88C-related disorder
RS61745604 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS745338278 Health Risk Conflicting classifications of pathogenicity
RS754233469 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS759310053 Health Risk Conflicting classifications of pathogenicity
RS762029178 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Hydrocephalus, nonsyndromic
RS769572282 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS77154172 Health Risk Conflicting classifications of pathogenicity CCDC88C-related disorder, CCDC88C-related disorder
RS772843353 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS78037497 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS78468999 Health Risk Conflicting classifications of pathogenicity
RS945447694 Health Risk Conflicting classifications of pathogenicity Hydrocephalus, nonsyndromic, autosomal recessive 1
RS1283433071 Health Risk Likely pathogenic Hydrocephalus, nonsyndromic, autosomal recessive 1
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