{"database":"EVA","file_versions":[{"headers":{"Content-Type":["application/json"]},"body":{"files":{"Vcf":["ftp://ftp.ebi.ac.uk/pub/databases/eva/PRJEB31123/PetersenOINewVariants.vcf.gz","ftp://ftp.ebi.ac.uk/pub/databases/eva/PRJEB31123/PetersenOINewVariants.accessioned.vcf.gz","ftp://ftp.ebi.ac.uk/pub/databases/eva/PRJEB31123/PetersenOINewVariants.vcf.gz.tbi"]},"type":"primary"},"statusCode":"OK","statusCodeValue":200}],"scores":{"citationCount":0,"reanalysisCount":0,"viewCount":0,"searchCount":0},"additional":{"dataset_type":["Whole Genome Sequencing"],"omics_type":["Genomics"],"submitter":["University of Nebraska-Lincoln"],"instrument_platform":["-"],"species":["Bos Taurus"],"full_dataset_link":["https://www.ebi.ac.uk/eva/?eva-study=PRJEB31123"],"repository":["EVA"],"name_synonyms":["Fragilitas, DYRK5, Disease, \"Osteogenesis imperfecta\" EXACT [SNOMEDCT_2005_07_31:254109004], Osteogenesis Imperfecta Tarda, Ossiums, Osteogenesis Imperfecta with Blue Sclerae, \"Osteogenesis imperfecta\" EXACT [SNOMEDCT_2005_07_31:205493000], CSA2., HMG-CoAR, Mutations, Germ Line, \"Osteogenesis imperfecta\" EXACT [SNOMEDCT_2005_07_31:254108007], Vrolik disease, Germline, Osteogenesis Imperfecta, \"brittle bone disease\" EXACT [CSP2005:1849-7175], Germ-Line Mutations, Lobstein Disease, \"Osteogenesis imperfecta\" EXACT [SNOMEDCT_2005_07_31:254105005], Type I, Germ Line Mutation, \"Vrolik's disease\" EXACT [SNOMEDCT_2005_07_31:205492005], \"Osteogenesis imperfecta NOS (disorder)\" EXACT [SNOMEDCT_2005_07_31:205498009], \"Osteogenesis imperfecta\" EXACT [ICD9CM_2006:756.51], Mutation, Fragilitas ossium, Lobsteins Disease, Fragilitas Ossium, hYAK3-2, Germline Mutations, OI, \"Fragilitas ossium\" EXACT [SNOMEDCT_2005_07_31:157008000], REDK, Germ-Line, Type 1, \"Osteogenesis imperfecta (disorder)\" EXACT [SNOMEDCT_2005_07_31:78314001], \"Osteopsathyrosis\" EXACT [MTHICD9_2006:756.51], Osteogenesis Imperfecta Tardas, \"Osteogenesis imperfecta\" EXACT [SNOMEDCT_2005_07_31:254106006], \"Osteogenesis imperfecta\" EXACT [SNOMEDCT_2005_07_31:254107002], Germline Mutation, \"Osteopsathyrosis (disorder)\" EXACT [SNOMEDCT_2005_07_31:205494006], Lobstein's Disease, RED, Red, \"Fragilitas ossium\" EXACT [SNOMEDCT_2005_07_31:268352002], Lobstein, Lobstein's, Brittle Bone Disease, Brittle bone disease"],"description_synonyms":["DYRK5, Taurine, dairy cow, Beef Cows, Materials, cow, Taurus Cattles, Bos indicus Cattles, Holstein Cow, Taurus Cattle, Gene, Cattle, Taurine Cattles, Indicine, Bos indicus, Dairy Cows, Cistrons, HMG-CoAR, CSA2, Domestic Cows., Bos grunniens, cattle, Bos taurus, Bos primigenius taurus, Genetic Materials, domestic cattle, Indicine Cattles, Yaks, Holstein, Genetic Material, Cattles, Yak, hYAK3-2, Genetic, Cows, Genomes, Domestic Cow, Dairy Cow, Bos bovis, INSDC_feature:gene, whole genome, Domestic, Dairy, Taurine Cattle, Beef, REDK, Bos Tauurus, Beef Cow, oxen, ox, Material, Cow, Taurus, RED, Red, Indicine Cattle, Cistron, Zebu, domestic cow, Zebus, Bos indicus Cattle, bovine"],"citation_count":["0"],"additional_accession":[]},"is_claimable":false,"name":"Evidence for a de novo, dominant germ-line mutation causative of osteogenesis imperfecta in two Red Angus calves","description":"Candidate gene evaluation through whole-genome sequencing of Red Angus cattle","dates":{"publication":"2019-02-07"},"accession":"PRJEB31123","cross_references":{"TAXONOMY":["9913"]}}