DDB2 Chromosome 11

Damage specific DNA binding protein 2
23 variants 23 Health Risk

Upload your DNA to see your personal genotypes for variants in DDB2.

What This Gene Does
This gene encodes a protein that is necessary for the repair of ultraviolet light-damaged DNA. This protein is the smaller subunit of a heterodimeric protein complex that participates in nucleotide excision repair, and this complex mediates the ubiquitylation of histones H3 and H4, which facilitates the cellular response to DNA damage. This subunit appears to be required for DNA binding. Mutations in this gene cause xeroderma pigmentosum complementation group E, a recessive disease that is characterized by an increased sensitivity to UV light and a high predisposition for skin cancer development, in some cases accompanied by neurological abnormalities. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2014]
Gene Info
Gene Group
"WD repeat domain containing|Xeroderma pigmentosum complementation groups|Nucleotide excision repair"
Locus Type
gene with protein product
Location
11p11.2
Ensembl
ENSG00000134574
Associated Conditions (5)
Xeroderma pigmentosum
group E
DDB2-related disorder
Ovarian cancer
Inborn genetic diseases
Key Variants
All Variants (23)
RSID Category Clinical Significance Conditions
RS138255134 Health Risk Conflicting classifications of pathogenicity Xeroderma pigmentosum, group E, Xeroderma pigmentosum
RS143049891 Health Risk Conflicting classifications of pathogenicity Xeroderma pigmentosum, group E, DDB2-related disorder
RS1953383789 Health Risk Conflicting classifications of pathogenicity Ovarian cancer, Ovarian cancer
RS199965459 Health Risk Conflicting classifications of pathogenicity Xeroderma pigmentosum, group E, Xeroderma pigmentosum
RS201703288 Health Risk Conflicting classifications of pathogenicity Xeroderma pigmentosum, group E, Xeroderma pigmentosum
RS373622283 Health Risk Conflicting classifications of pathogenicity Xeroderma pigmentosum, group E, Inborn genetic diseases
RS374094218 Health Risk Conflicting classifications of pathogenicity Xeroderma pigmentosum, group E, Xeroderma pigmentosum
RS549041558 Health Risk Conflicting classifications of pathogenicity Xeroderma pigmentosum, group E, Xeroderma pigmentosum
RS55847708 Health Risk Conflicting classifications of pathogenicity Xeroderma pigmentosum, group E, Xeroderma pigmentosum
RS61741581 Health Risk Conflicting classifications of pathogenicity Xeroderma pigmentosum, group E, Xeroderma pigmentosum
RS753070223 Health Risk Conflicting classifications of pathogenicity Xeroderma pigmentosum, Xeroderma pigmentosum
RS1953668281 Health Risk Likely pathogenic
RS2540389596 Health Risk Likely pathogenic Xeroderma pigmentosum, group E, Xeroderma pigmentosum
RS2540393834 Health Risk Likely pathogenic
RS121434639 Health Risk Pathogenic Xeroderma pigmentosum, group E, Xeroderma pigmentosum
RS121434641 Health Risk Pathogenic Xeroderma pigmentosum, group E, Xeroderma pigmentosum
RS121434642 Health Risk Pathogenic Xeroderma pigmentosum, group E, Xeroderma pigmentosum
RS1218859102 Health Risk Pathogenic
RS144989465 Health Risk Pathogenic
RS199822504 Health Risk Pathogenic
RS781655324 Health Risk Pathogenic Xeroderma pigmentosum, group E, Xeroderma pigmentosum
RS121434640 Health Risk Pathogenic/Likely pathogenic Xeroderma pigmentosum, group E, Xeroderma pigmentosum
RS1336484333 Health Risk Pathogenic/Likely pathogenic Xeroderma pigmentosum, group E, Xeroderma pigmentosum
Sign Up to Analyze Your DNA Log In