MOESM2 of A reverse genetic approach identifies an ancestral frameshift mutation in RP1 causing recessive progressive retinal degeneration in European cattle breeds
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https://figshare.com/articles/dataset/MOESM2_of_A_reverse_genetic_approach_identifies_an_ancestral_frameshift_mutation_in_RP1_causing_recessive_progressive_retinal_degeneration_in_European_cattle_breeds/4462307
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Additional file 2: Table S2. Details on non-rare putative deleterious variants selected in 15 breeds from the 1000 bull genomes run4 dataset. This file contains the list of the 2489 variants selected in this study. For each of them, we indicate: (i) the frequency in each breed, (ii) the functional consequence on the protein, and (iii) the genetic syndromes associated with mutations within the same gene in human (Online Mendelian Inheritance in Man, OMIM; http://www.omim.org ) and mouse (Mammalian Phenotypes; http://www.informatics.jax.org ). AAN: Aberdeen-Angus, BBR: Beef Booster Composite, BSW: Brown Swiss, CHA: Charolais, GVH: Gelbvieh, HER: Hereford, HOL: Holstein, JER: Jersey, LIM: Limousine, MON: Montbéliarde, NOR: Normande, RAN: Red Angus, RDCF: Finnish Red, RDCS: Swedish Red, and SIM: Simmental.
创建时间:
2016-12-16



