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281
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|
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RAD23 nucleotide excision repair protein B |
HHR23B, HR23B, P58 |
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282
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RAD51 recombinase |
BRCC5, FANCR, HRAD51, HsRad51, HsT16930, MRMV2, RAD51A, RECA |
Agenesis of corpus callosum, Anxiety disorder, Astigmatism, Atrial septal defect, Azoospermia, Breast cancer, Mammary neoplasms, Breast carcinoma, Cafe-au-lait spot, Camptodactyly of fingers, Cataract, Cerebral palsy, Choanal atresia, Congenital arteriovenous malformation, Congenital epicanthus, Congenital exomphalos, Congenital mirror movements, Cranial nerve paralysis, Cryptorchidism, Developmental delay, Dolichocephaly, Dwarfism, Dysgenesis of the hippocampus, Dysmorphic features, Fanconi anemia, Frontal bossing, Head and neck neoplasms, Head neoplasms, Neck cancer, Neoplasm of head, Hereditary breast and ovarian cancer syndrome, High palate, Hirschsprung disease, Hydrocephalus, Hypertrophic cardiomyopathy, Hypogonadism, Hypogonadotropic hypogonadism, Hypospadias, Imperforate anus, Leukemia, Leukopenia, Head and neck cancer, Marfan syndrome, Meckel diverticulum, Melanoma, Mental retardation, Microcephaly, Micrognathism, Microphthalmos, Miller dieker syndrome, Mirror movements, Monocytic leukemia, Myelodysplasia, Myelodysplastic syndrome, Myopia, Neck neoplasms, Nystagmus, Ovarian neoplasm, Pancreatic neoplasm, Patent ductus arteriosus, Peritoneal carcinoma, Phakomatosis pigmentovascularis, Proptosis, Prostate cancer, Ptosis, Radial polydactyly, Renal insufficiency, Scoliosis, Specific learning disorder, Spina bifida, Strabismus, Syndactyly of fingers, Syndactyly of the toes, Tetralogy of fallot, Upper aerodigestive tract neoplasmsView all (60 more) |
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283
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RAD51 paralog C |
BROVCA3, FANCO, R51H3, RAD51L2 |
Astigmatism, Atrial septal defect, Azoospermia, Breast cancer, Breast carcinoma, Cafe-au-lait spot, Camptodactyly of fingers, Cataract, Choanal atresia, Congenital arteriovenous malformation, Congenital atresia of rectum, Congenital epicanthus, Congenital exomphalos, Congenital heart defects, Congenital hypoplasia of radius, Cranial nerve paralysis, Cryptorchidism, Developmental delay, Dolichocephaly, Dwarfism, Fanconi anemia, Frontal bossing, Hereditary breast and ovarian cancer syndrome, Hereditary cancer syndrome, High palate, Hirschsprung disease, Hydrocephalus, Hydronephrosis, Hypertrophic cardiomyopathy, Hypogonadism, Hypoplasia of thumb, Hypospadias, Imperforate anus, Kidney disease, Leukemia, Leukopenia, Mammary neoplasms, Marfan syndrome, Meckel diverticulum, Melanoma, Mental retardation, Microcephaly, Micrognathism, Microphthalmos, Miller dieker syndrome, Monocytic leukemia, Myelodysplasia, Myelodysplastic syndrome, Nystagmus, Ovarian cancer, Ovarian carcinoma, Ovarian epithelial carcinoma, Ovarian neoplasm, Pancreatic neoplasm, Pancytopenia, Patent ductus arteriosus, Peritoneal carcinoma, Proptosis, Prostate cancer, Ptosis, Renal cyst, Renal insufficiency, Scoliosis, Spina bifida, Strabismus, Syndactyly of fingers, Syndactyly of the toes, Tetralogy of fallot, Thumb aplasiaView all (54 more) |
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284
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RAD51 paralog B |
R51H2, RAD51L1, REC2 |
Asthma, Biliary cirrhosis, Breast cancer, Breast carcinoma, male, Neoplasm of male breast, Mammary neoplasms, Breast carcinoma, Hereditary cancer syndrome, Colonic neoplasms, Colorectal cancer, Colorectal neoplasms, Eczema, Exudative macular degeneration, Geographic atrophy, Hereditary breast and ovarian cancer syndrome, Hypothyroidism, Leukemia, Lung carcinoma, Lung adenocarcinoma, Lupus erythematosus, Age-related macular degeneration, Marfan syndrome, Nasopharyngeal carcinoma, Ovarian neoplasm, Ovarian serous adenocarcinoma, Ovarian endometrioid carcinoma, Prostate cancer, Respiratory tract diseases, Rheumatoid arthritisView all (14 more) |
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285
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|
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RAD51 paralog D |
BROVCA4, R51H3, RAD51L3, TRAD |
Breast cancer, Breast carcinoma, Hereditary cancer syndrome, Chromosome deletion, Colorectal cancer, Hereditary breast and ovarian cancer syndrome, Melanoma, Ovarian neoplasm, Ovarian cancer, Pancreatic neoplasm, Peritoneal carcinoma, Prostate cancer |
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286
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|
|
RAD52 DNA repair protein |
- |
|
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287
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|
|
Raf-1 proto-oncogene, serine/threonine kinase |
CMD1NN, CRAF, NS5, Raf-1, c-Raf |
Abnormal dermatoglyphic pattern, Anomalous pulmonary artery, Atrial septal defect, Brachycephaly, Brachydactyly, Breast cancer, Breast carcinoma, Bundle branch block, Camptodactyly of fingers, Cardiofaciocutaneous syndrome, Cardiomyopathy, Colorectal neoplasms, Congenital epicanthus, Congenital pectus carinatum, Congenital pectus excavatum, Costello syndrome, Cryptorchidism, Cubitus valgus, Cystic hygroma, Developmental delay, Dilated cardiomyopathy, Dolichocephaly, Dwarfism, Dysarthria, Dysmorphic features, Gastric cancer, Gastroesophageal reflux disease, Glioma, Hearing loss, High palate, Hypertrophic cardiomyopathy, Hypogonadotropic hypogonadism, Hypospadias, Kidney cancer, Kidney neoplasm, Leopard syndrome, Lipoatrophy, Lipodystrophy, Liver cancer, Liver neoplasms, Lung adenocarcinoma, Lung cancer, Lung carcinoma, Lung neoplasms, Macrocephaly, Macrostomia, Malignant mesothelioma, Malocclusion, Mammary neoplasms, Marfan syndrome, Melanocytic nevus, Melanoma, Mental retardation, Micrognathism, Mitral valve prolapse, Multiple congenital anomalies, Multiple lentigines, Myelodysplasia, Myelodysplastic syndrome, Myocardial infarction, Myopathy, Neck webbing, Neuroblastoma, Noonan syndrome, Noonan syndrome with multiple lentigines, Noonan-like syndrome with loose anagen hair, Nystagmus, Ovarian epithelial carcinoma, Ovarian serous adenocarcinoma, Palmoplantar keratoderma, Phakomatosis pigmentovascularis, Pilomyxoid astrocytoma, Posteriorly rotated ear, Proptosis, Ptosis, Pulmonary stenosis, Radioulnar synostosis, Scoliosis, Spina bifida occulta, Sprengel deformity, Strabismus, Turner syndrome, male, Ventricular septal defectView all (68 more) |
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288
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|
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Recombination activating 1 |
RAG-1, RNF74 |
Alopecia, Anemia, Arthritis, Autoimmune hemolytic anemia, Combined cellular and humoral immune defects with granulomas, Congenital hypoplasia of thymus, Conjunctivitis, Eosinophilia, Exfoliative dermatitis, Hypoproteinemia, Hypothyroidism, Immunologic deficiency syndromes, Lymphadenitis, Lymphoma, Mastoiditis, Nephrotic syndrome, Omenn syndrome, Otitis media, Immunodeficiency, Prostatic neoplasms, Prostate cancer, Reticuloendotheliosis with eosinophilia, Severe combined immunodeficiency disease, ThyroiditisView all (9 more) |
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289
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|
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Recombination activating 2 |
RAG-2 |
Alopecia, Anemia, Arthritis, Autoimmune hemolytic anemia, Combined cellular and humoral immune defects with granulomas, Congenital hypoplasia of thymus, Conjunctivitis, Eosinophilia, Exfoliative dermatitis, Hypoproteinemia, Hypothyroidism, Immunologic deficiency syndromes, Lymphadenitis, Lymphoma, Mastoiditis, Nephrotic syndrome, Non-alcoholic fatty liver disease, Omenn syndrome, Otitis media, Immunodeficiency, Reticuloendotheliosis with eosinophilia, Severe combined immunodeficiency disease, ThyroiditisView all (8 more) |
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290
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RAS like proto-oncogene A |
HINCONS, RAL |
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