Gene entry
CARD14
caspase recruitment domain family member 14
- Chromosome
- 17
- Cytoband
- 17q25.3
- Variants (rsID)
- 20
CARD14 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 17 (region 17q25.3). Its official name is “caspase recruitment domain family member 14”. The reference table lists 20 variants (rsID) for this gene.
Clinically classified variants
9 reference-table entries with clinical significance.
- rs11652075Benignsingle nucleotide variantPityriasis rubra pilaris|Psoriasis 2|Pityriasis rubra pilaris|Psoriasis 2|Autoinflammatory syndrome
- rs117918077Benignsingle nucleotide variantPityriasis rubra pilaris|Psoriasis 2|Autoinflammatory syndrome
- rs144475004Benignsingle nucleotide variantPityriasis rubra pilaris|Psoriasis 2|Autoinflammatory syndrome
- rs61751629Benignsingle nucleotide variantPityriasis rubra pilaris|Psoriasis 2|Autoinflammatory syndrome
- rs61751630Benignsingle nucleotide variantPityriasis rubra pilaris|Psoriasis 2|Autoinflammatory syndrome
- rs73429414Benignsingle nucleotide variantPityriasis rubra pilaris|Psoriasis 2|Autoinflammatory syndrome
- rs74000616Benignsingle nucleotide variantPityriasis rubra pilaris|Psoriasis 2|Autoinflammatory syndrome
- rs104894635Pathogenicsingle nucleotide variantMucopolysaccharidosis, MPS-III-A|Sanfilippo syndrome|Inborn genetic diseases|Mucopolysaccharidosis|Neurodegeneration
- rs139466192Uncertain significancesingle nucleotide variantPsoriasis 2|Pityriasis rubra pilaris|Autoinflammatory syndrome
Other listed variants
Public references
Data from the institutional reference table and public NCBI annotation. For education only; not a substitute for medical or genetic counselling.