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uv(Ultra violet) |
Sources:
Effects:
Species:
Is connected with following human diseases:
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ATAXIA-TELANGIECTASIA (208900)
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BLOOM SYNDROME; BLM (#210900 )
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BREAST CANCER (114480 )
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COCKAYNE SYNDROME, TYPE A (#216400 )
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XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP E (#601675 )
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TRICHOTHIODYSTROPHY, PHOTOSENSITIVE (#601675 )
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XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP G (#278780 )
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COCKAYNE SYNDROME, TYPE B (#133540 )
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FANCONI ANEMIA (#227650 )
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FANCONI ANEMIA, COMPLEMENTATION GROUP C (227645)
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MUIR-TORRE SYNDROME (#158320 )
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LYNCH SYNDROME I (#120435 )
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XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP A (#278700 )
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XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP D (#278730 )
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MISMATCH REPAIR CANCER SYNDROME (#276300 )
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ESOPHAGEAL CANCER (#133239 )
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COLORECTAL CANCER (#114500 )
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SECKEL SYNDROME 1 (#210600 )
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CEREBROOCULOFACIOSKELETAL SYNDROME 4 (#610758 )
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LIG4 SYNDROME (#606593 )
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ENDOMETRIAL CANCER (#608089 )
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PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHON (#157640 )
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BALLER-GEROLD SYNDROME; BGS (218600 )
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XERODERMA PIGMENTOSUM, VARIANT TYPE; XPV (#278750 )
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PROSTATE CANCER (#176807)
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GASTRIC CANCER (137215 )
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SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE, WITH (#607250 )
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FANCONI ANEMIA, COMPLEMENTATION GROUP D2 (+227646 )
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IMMUNODEFICIENCY WITH HYPER-IgM, TYPE 5 (#608106 )
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RS-SCID (602450 )
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SEVERE COMBINED IMMUNODEFICIENCY WITH MICROCEPHALY (611291)
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ATAXIA-TELANGIECTASIA-LIKE DISORDER; ATLD (604391)
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NIJMEGEN BREAKAGE SYNDROME, NBS (251260)
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COLORECTAL CANCER, HEREDITARY NONPOLYPOSIS, TYPE 2 (#609310)
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COLORECTAL CANCER, HEREDITARY NONPOLYPOSIS, TYPE 4 (+600259)
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COLORECTAL CANCER, HEREDITARY NONPOLYPOSIS, TYPE 3 (+600258)
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COLORECTAL CANCER, HEREDITARY NONPOLYPOSIS, TYPE 5 (600678)
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WERNER SYNDROME, WRN (#277700 )
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ROTHMUND-THOMSON SYNDROME; RTS (#268400)
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ATAXIA-OCULOMOTOR APRAXIA 1 (208920)
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RIDDLE Syndrome (611943)
Keywords:
- nucleotide excision repair (NER)
- DNA damage tolerance pathway (TLS)
- base excision repair (BER)
- cell cycle checkpoint control
- response to DNA damage
Last modification of this entry: March 28, 2012.
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