Genetic investigations for limb malformations in Holstein cattle.
收藏NIAID Data Ecosystem2026-03-11 收录
官方服务：
资源简介：
Whole-genome sequencing data of Holstein cattle were investigated for limb malformations.
应用场景：
创建时间：
2020-04-14
相关数据集
MOESM3 of Confirmation of a non-synonymous SNP in PNPLA8 as a candidate causal mutation for Weaver syndrome in Brown Swiss cattle
Additional file 3: Table S1. Genotype distribution of 41 candidate causal mutations for Weaver syndrome in 1147 animals. The distribution of the genotypes of 41 candidate causal mutations (McClure et
Figshare2016-12-16 更新70
Genotyping results for RNF34 and KDM2B mutations.
aCattle recorded as parent of affected calves.bFor this cow only one single suspicious offspring was recorded by the breeding organization and the diagnosis of this calf had not been confirmed by necr
Figshare2015-12-02 更新40
Table S5. ARRDC3 and NFIA genotypes for two SNPs from the 1203 animals and 46 breeds listed in Table 4.
Bovine congestive heart failure (BCHF) has become increasingly prevalent among feedlot cattle in the Western Great Plains of North America with up to 7% mortality in affected herds. BCHF is an untreat
Figshare2024-01-11 更新40
A missense mutation in TUBD1 is associated with high juvenile mortality in Braunvieh and Fleckvieh cattle
Background Haplotypes with reduced or missing homozygosity may harbor deleterious alleles that compromise juvenile survival. A scan for homozygous haplotype deficiency revealed a short segment on bovi
NIAID Data Ecosystem60
Identification and prevalence of a genetic defect that causes leukocyte adhesion deficiency in Holstein cattle.
Two point mutations were identified within the gene encoding bovine CD18 in a Holstein calf afflicted with leukocyte adhesion deficiency (LAD). One mutation causes an aspartic acid to glycine substitu
PubMed Central1992-10-01 更新40
