Homozygous haplotype deficiency reveals deleterious mutations compromising reproductive and rearing success in cattle

BMC Genomics

Volumn 16, Issue 1, 2015, Pages

  Pausch, Hubert ^a   Schwarzenbacher, Hermann ^b   Burgstaller, Johann ^c   Flisikowski, Krzysztof ^a   Wurmser, Christine ^a   Jansen, Sandra ^a   Jung, Simone ^a   Schnieke, Angelika ^a   Wittek, Thomas ^c   Fries, Ruedi ^a  

^a TECHNICAL UNIVERSITY OF MUNICH   (Germany)

^b ZucbtData EDV Dienstleistungen GmbH   (Austria)

^c UNIVERSITY OF VETERINARY MEDICINE   (Austria)

Author keywords

Embryonic lethality; Fanconi Bickel syndrome; Homozygous haplotype deficiency; SLC2A2; SUGT1

Indexed keywords

ANIMALIA; BOS;

CELL CYCLE PROTEIN; GLUCOSE TRANSPORTER 2; RNA SPLICING;

ALLELE; AMINO ACID SEQUENCE; ANIMAL; ARTIFICIAL INSEMINATION; BOVINE; CHEMISTRY; FANCONI RENOTUBULAR SYNDROME; FRAMESHIFT MUTATION; GENETICS; GENOME; GENOTYPE; HAPLOTYPE; HOMOZYGOTE; HUMAN; METABOLISM; MISSENSE MUTATION; MOLECULAR GENETICS; MUTATION; NUCLEOTIDE SEQUENCE; PATHOLOGY; PHENOTYPE; RNA SPLICING; SEQUENCE ALIGNMENT; VETERINARY;

ALLELES; AMINO ACID SEQUENCE; ANIMALS; BASE SEQUENCE; CATTLE; CELL CYCLE PROTEINS; FANCONI SYNDROME; FRAMESHIFT MUTATION; GENOME; GENOTYPE; GLUCOSE TRANSPORTER TYPE 2; HAPLOTYPES; HOMOZYGOTE; HUMANS; INSEMINATION, ARTIFICIAL; MOLECULAR SEQUENCE DATA; MUTATION; MUTATION, MISSENSE; PHENOTYPE; RNA SPLICE SITES; SEQUENCE ALIGNMENT;

EID: 84928011841     PISSN: None     EISSN: 14712164     Source Type: Journal    
DOI: 10.1186/s12864-015-1483-7     Document Type: Article

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