Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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10821 to 10830 of 15448 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

10821
RAD18 E3 ubiquitin protein ligase
RNF73
Color vision deficiency, Uterine fibroid

10822
RAD21 cohesin complex component
CDLS4, HR21, HRAD21, MCD1, MGS, NXP1, SCC1, hHR21
Cornelia de lange syndrome, De lange syndrome, Desbuquois syndrome, Myeloid leukemia, Schizoaffective disorder, Trichorhinophalangeal syndrome

10823
RAD21 cohesin complex component like 1
RAD21L, dJ545L17.2
Autoimmune thrombocytopenic purpura, Color vision deficiency, Multiple sclerosis, Oligodendroglioma, Testicular azoospermia

10824
RAD23 nucleotide excision repair protein A
HHR23A, HR23A
Stomach neoplasms

10825
RAD23 nucleotide excision repair protein B
HHR23B, HR23B, P58
Atrial fibrillation, Obstructive pulmonary disease, Craniofacial abnormalities, Male infertility, Alzheimer disease, Prostate cancer, Prostatic neoplasms

10826
RAD50 double strand break repair protein
NBSLD, RAD502, hRad50
Asthma, Eczema, Cardiovascular disease, Crohn disease, Eosinophilia, Ovarian cancer, Hereditary breast and ovarian cancer syndrome, Hereditary breast cancer, Inflammatory bowel disease, Inflammatory skin disease, Psoriasis, Seasonal allergic rhinitis, Ulcerative colitis, Venous thromboembolism

10827
RAD51 recombinase
BRCC5, FANCR, HRAD51, HsRad51, HsT16930, MRMV2, RAD51A, RECA
Anxiety disorder, Breast neoplasms, Breast cancer, Congenital mirror movements, Fanconi anemia, Genetic predisposition to disease, Head and neck neoplasms, Hereditary breast and ovarian cancer syndrome, Hereditary breast cancer, Mirror movements, Prostate cancer

10828
RAD51 associated protein 2
-
Crohn disease, Inflammatory bowel disease, Ulcerative colitis

10829
RAD51 paralog B
R51H2, RAD51L1, REC2
Androgenetic alopecia, Angioedema, Asthma, Atrophic macular degeneration, Autoimmune thyroid disease, Biliary cirrhosis, Biliary tract cancer, Breast cancer, Breast neoplasms, Male breast neoplasms, Cancer, Central nervous system cancer, Cervical cancer, Obstructive pulmonary disease, Color vision deficiency
View all (34 more)

10830
RAD51 paralog C
BROVCA3, FANCO, R51H3, RAD51L2
Breast neoplasms, Hereditary breast-ovarian cancer syndrome, Fanconi anemia, Hereditary breast and ovarian cancer syndrome, Premature ovarian failure, Ovarian neoplasms