Functional relevance of naturally occurring mutations in adhesion G protein-coupled receptor ADGRD1 (GPR133)

BMC Genomics

Volumn 17, Issue 1, 2016, Pages

  Fischer, Liane ^a   Wilde, Caroline ^a   Schöneberg, Torsten ^a   Liebscher, Ines ^a  

^a UNIVERSITY OF LEIPZIG   (Germany)

Author keywords

ADGRD1; Adhesion GPCR; Database; GPR133; Mutations; SNP

Indexed keywords

ADGRD1 GENE; ARTICLE; CONTROLLED STUDY; EXON; FRAMESHIFT MUTATION; GENE ACTIVITY; GENE SEQUENCE; GENETIC ASSOCIATION; GENETIC VARIABILITY; HUMAN; MISSENSE MUTATION; PHENOTYPE; SINGLE NUCLEOTIDE POLYMORPHISM; AMINO ACID SUBSTITUTION; ANIMAL; ASYMPTOMATIC DISEASE; BODY HEIGHT; CHLOROCEBUS AETHIOPS; COS CELL LINE; GENE EXPRESSION; GENETIC DATABASE; GENETICS; GENOME-WIDE ASSOCIATION STUDY; HEART RATE; HEK293 CELL LINE; HUMAN GENOME; MUTATION;

G PROTEIN COUPLED RECEPTOR; GPR133 PROTEIN, HUMAN;

AMINO ACID SUBSTITUTION; ANIMALS; ASYMPTOMATIC DISEASES; BODY HEIGHT; CERCOPITHECUS AETHIOPS; COS CELLS; DATABASES, GENETIC; EXONS; GENE EXPRESSION; GENOME, HUMAN; GENOME-WIDE ASSOCIATION STUDY; HEART RATE; HEK293 CELLS; HUMANS; MUTATION; POLYMORPHISM, SINGLE NUCLEOTIDE; RECEPTORS, G-PROTEIN-COUPLED;

EID: 84991813256     PISSN: None     EISSN: 14712164     Source Type: Journal    
DOI: 10.1186/s12864-016-2937-2     Document Type: Article

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