An intronic SINE insertion in FAM161A that causes exon-skipping is associated with progressive retinal atrophy in Tibetan Spaniels and Tibetan Terriers

PLoS ONE

Volumn 9, Issue 4, 2014, Pages

  Downs, Louise M ^a   Mellersh, Cathryn S ^a  

^a ANIMAL HEALTH TRUST   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

MESSENGER RNA; EYE PROTEIN; FAM161A PROTEIN, HUMAN;

ANIMAL EXPERIMENT; ANIMAL TISSUE; ARTICLE; ATROPHY; BINDING SITE; CONTROLLED STUDY; DNA FLANKING REGION; DOG BREED; EXON SKIPPING; FAM161A GENE; FRAMESHIFT MUTATION; GENE; GENE IDENTIFICATION; GENE INSERTION; GENE LOCUS; GENE MUTATION; GENE SEGREGATION; GENETIC ASSOCIATION; GENETIC HETEROGENEITY; HOMOZYGOSITY; INTRON; NONHUMAN; NUCLEOTIDE SEQUENCE; PROGRESSIVE RETINAL ATROPHY; RETINA DISEASE; RNA ANALYSIS; SHORT INTERSPERSED REPEAT; STOP CODON; TIBETAN SPANIEL; TIBETAN TERRIER; ALTERNATIVE RNA SPLICING; ANIMAL; CHROMOSOME MAP; DOG; EXON; GENE EXPRESSION REGULATION; GENETIC DISORDER; GENETIC TRANSCRIPTION; GENETICS; GENOTYPE; MOLECULAR GENETICS; MUTATION; RETINA DEGENERATION;

ALTERNATIVE SPLICING; ANIMALS; BASE SEQUENCE; CHROMOSOME MAPPING; DOGS; EXONS; EYE PROTEINS; GENE EXPRESSION REGULATION; GENETIC DISEASES, INBORN; GENOME-WIDE ASSOCIATION STUDY; GENOTYPE; INTRONS; MOLECULAR SEQUENCE DATA; MUTAGENESIS, INSERTIONAL; MUTATION; RETINAL DEGENERATION; SHORT INTERSPERSED NUCLEOTIDE ELEMENTS; TRANSCRIPTION, GENETIC;

EID: 84899121227     PISSN: None     EISSN: 19326203     Source Type: Journal    
DOI: 10.1371/journal.pone.0093990     Document Type: Article

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