Several classical mouse inbred strains, including DBA/2, NOD/Lt, FVB/N, and SJL/J, carry a putative loss-of-function Allele of Gpr84

Journal of Heredity

Volumn 104, Issue 4, 2013, Pages 565-571

  Perez, Carlos J ^a,b   Dumas, Aline ^c   Vallières, Luc ^c   Guénet, Jean Louis ^d   Benavides, Fernando ^a,b  

^a UNIVERSITY OF TEXAS   (United States)

^b UNIVERSITY OF TEXAS   (United States)

^c LAVAL UNIVERSITY   (Canada)

^d INSTITUT PASTEUR   (France)

Author keywords

G protein coupled receptors; inbred mice; mouse models; spontaneous mutations

Indexed keywords

ALLELE; ARTICLE; EXON; FRAMESHIFT MUTATION; GENE DELETION; GENE SEQUENCE; HAPLOTYPE; HOMOZYGOSITY; LOSS OF FUNCTION MUTATION; MOUSE; MOUSE STRAIN; NONHUMAN; NONSENSE MUTATION; PREMATURITY; PRIORITY JOURNAL; PROTEIN DOMAIN; STOP CODON; WILD TYPE;

G PROTEIN-COUPLED RECEPTORS; INBRED MICE; MOUSE MODELS; SPONTANEOUS MUTATIONS;

ALLELES; ANIMALS; BASE SEQUENCE; CODON, NONSENSE; MICE; MICE, INBRED C3H; MICE, INBRED C57BL; MICE, INBRED DBA; MICE, INBRED NOD; MOLECULAR SEQUENCE DATA; PHYLOGENY; RECEPTORS, G-PROTEIN-COUPLED; SEQUENCE DELETION; SPECIES SPECIFICITY;

MUS; MUS MUSCULUS DOMESTICUS;

EID: 84879144910     PISSN: 00221503     EISSN: 14657333     Source Type: Journal    
DOI: 10.1093/jhered/est023     Document Type: Article

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