Bovine exome sequence analysis and targeted SNP genotyping of recessive fertility defects BH1, HH2, and HH3 reveal a putative causative mutation in SMC2 for HH3

PLoS ONE

Volumn 9, Issue 3, 2014, Pages

  McClure, Matthew C ^a   Bickhart, Derek ^a   Null, Dan ^a   VanRaden, Paul ^a   Xu, Lingyang ^a   Wiggans, George ^a   Liu, George ^a   Schroeder, Steve ^a   Glasscock, Jarret ^b   Armstrong, Jon ^b   Cole, John B ^a   Van Tassell, Curtis P ^a   Sonstegard, Tad S ^a  

^a AGRICULTURAL RESEARCH SERVICE   (United States)

^b United States Department of Agriculture Agriculture Research Service Animal Improvement Programs Laboratory ^*  (United States)

Author keywords

[No Author keywords available]

Indexed keywords

PHENYLALANINE; SERINE; NUCLEAR PROTEIN;

AMINO ACID SUBSTITUTION; ARTICLE; BROWN SWISS HAPLOTYPE 1; CATTLE; CELL DIVISION; CHROMOSOME 8; CHROMOSOME CONDENSATION; CHROMOSOME SEGREGATION; CONTROLLED STUDY; COPY NUMBER VARIATION; DNA REPAIR; EMBRYO DEVELOPMENT; EXOME; FERTILITY; GENE; GENETIC PROCEDURES; GENETIC VARIABILITY; GENOTYPE; HAPLOTYPE; HAPLOTYPE MAP; HETEROZYGOSITY; HOLSTEIN HAPLOTYPE 2; HOLSTEIN HAPLOTYPE 3; HOMOZYGOSITY; MOLECULAR EVOLUTION; NEXT GENERATION SEQUENCING; NONHUMAN; PROTEIN DOMAIN; SINGLE NUCLEOTIDE POLYMORPHISM; SMC2 GENE; ANIMAL; BOVINAE; CHROMOSOME; FEMALE; GENETICS; MALE; NUCLEOTIDE SEQUENCE; POINT MUTATION;

ANIMALS; CATTLE; CHROMOSOMES, MAMMALIAN; DNA MUTATIONAL ANALYSIS; DNA REPAIR; EXOME; FEMALE; HAPLOTYPES; MALE; NUCLEAR PROTEINS; POINT MUTATION; POLYMORPHISM, SINGLE NUCLEOTIDE;

EID: 84899789226     PISSN: None     EISSN: 19326203     Source Type: Journal    
DOI: 10.1371/journal.pone.0092769     Document Type: Article

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