Gene | Disease | Score gda | Association Type | Original DB | Sentence supporting the association | PMID | PMID Year | ||||||||
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0.430 | Biomarker | GENOMICS_ENGLAND | |||||||||||
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0.430 | Biomarker | GENOMICS_ENGLAND | |||||||||||
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0.430 | Biomarker | GENOMICS_ENGLAND | |||||||||||
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0.430 | Biomarker | GENOMICS_ENGLAND | |||||||||||
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0.430 | Biomarker | GENOMICS_ENGLAND | |||||||||||
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0.440 | Biomarker | GENOMICS_ENGLAND | |||||||||||
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0.440 | Biomarker | GENOMICS_ENGLAND | |||||||||||
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0.440 | Biomarker | GENOMICS_ENGLAND | |||||||||||
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0.440 | Biomarker | GENOMICS_ENGLAND | |||||||||||
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0.450 | Biomarker | GENOMICS_ENGLAND | |||||||||||
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0.460 | Biomarker | GENOMICS_ENGLAND | |||||||||||
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0.470 | Biomarker | GENOMICS_ENGLAND | Negative regulation of ciliary length by ciliary male germ cell-associated kinase (Mak) is required for retinal photoreceptor survival. | 21148103 | 2010 |
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0.470 | Biomarker | GENOMICS_ENGLAND | Apoptosis-inducing signal sequence mutation in carbonic anhydrase IV identified in patients with the RP17 form of retinitis pigmentosa. | 15090652 | 2004 |
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0.480 | Biomarker | GENOMICS_ENGLAND | |||||||||||
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0.490 | Biomarker | GENOMICS_ENGLAND | |||||||||||
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0.500 | Biomarker | GENOMICS_ENGLAND | Novel association of RP1 gene mutations with autosomal recessive retinitis pigmentosa. | 15863674 | 2005 |
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0.500 | Biomarker | GENOMICS_ENGLAND | |||||||||||
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0.500 | Biomarker | GENOMICS_ENGLAND | |||||||||||
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0.500 | Biomarker | GENOMICS_ENGLAND | |||||||||||
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0.500 | Biomarker | GENOMICS_ENGLAND | |||||||||||
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0.500 | Biomarker | GENOMICS_ENGLAND | |||||||||||
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0.510 | Biomarker | GENOMICS_ENGLAND | Mouse Idh3a mutations cause retinal degeneration and reduced mitochondrial function. | 30478029 | 2018 |
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0.510 | Biomarker | GENOMICS_ENGLAND | |||||||||||
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0.510 | Biomarker | GENOMICS_ENGLAND | |||||||||||
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0.520 | Biomarker | GENOMICS_ENGLAND | Mutation screening of the GUCA1B gene in patients with autosomal dominant cone and cone rod dystrophy. | 21405999 | 2011 |