Catalog of 238 variations among six human genes encoding solute carriers (hSLCs) in the Japanese population

Journal of Human Genetics

Volumn 47, Issue 11, 2002, Pages 576-584

  Saito, Susumu ^a   Iida, Aritoshi ^a   Sekine, Akihiro ^a   Ogawa, Chie ^b   Kawauchi, Saori ^a   Higuchi, Shoko ^a   Nakamura, Yusuke ^a,b  

^a INST OF PHYS AND CHEMICAL RESEARCH   (Japan)

^b UNIVERSITY OF TOKYO   (Japan)

Author keywords

SLC10A1; SLC15A1; SLC22A1; SLC22A2; SLC22A4; SLC22A5; SNP

Indexed keywords

ORGANIC CATION TRANSPORTER 1; ORGANIC CATION TRANSPORTER 2; PEPTIDE TRANSPORTER 1; PROTEIN; PROTEIN SLC; PROTEIN SLC10A1; PROTEIN SLC22A4; PROTEIN SLC22A5; UNCLASSIFIED DRUG; CARNITINE TRANSPORTER 1; CARNITINE TRANSPORTER 2; DNA; GENOMIC DNA; SODIUM BILE ACID COTRANSPORTER; SOLUTE CARRIER PROTEIN;

ARTICLE; CHROMOSOMAL LOCALIZATION; CLINICAL ARTICLE; DISEASE PREDISPOSITION; DNA FLANKING REGION; DNA SCREENING; DNA SEQUENCE; EXON; GENE DELETION; GENE INSERTION; GENETIC POLYMORPHISM; GENETIC VARIABILITY; GENOTYPE; HUMAN; HUMAN GENOME; INTRON; JAPAN; PHENOTYPE; PROMOTER REGION; SINGLE NUCLEOTIDE POLYMORPHISM; 3' FLANKING REGION; 5' FLANKING REGION; CONTROLLED STUDY; GENE; GENE IDENTIFICATION; GENE SEQUENCE; GENETIC CODE; GENETIC SCREENING; GENETIC VARIATION; GENOTYPE PHENOTYPE CORRELATION; HUMAN CELL; INDEL MUTATION; JAPANESE (PEOPLE); SLC10A1 GENE; SLC15A1 GENE; SLC22A1 GENE; SLC22A2 GENE; SLC22A4 GENE; SLC22A5 GENE;

INSERTION SEQUENCES;

EID: 0036952563     PISSN: 14345161     EISSN: None     Source Type: Journal    
DOI: 10.1007/s100380200088     Document Type: Article

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