Gene: SLCO1B3-SLCO1B7

Alternate names for this Gene: LST-3TM12|OATP1B3-1B7

Gene Summary: This locus represents naturally occurring readthrough transcription between the neighboring SLCO1B3 (solute carrier organic anion transporter family member 1B3) and SLCO1B7 (solute carrier organic anion transporter family member 1B7 (putative)) genes on chromosome 12. The readthrough transcript encodes a protein that shares sequence identity with both the upstream and downstream genes.

Gene is located in Chromosome: 12

Location in Chromosome : 12p12.2

Description of this Gene: SLCO1B3-SLCO1B7 readthrough

Type of Gene: protein-coding

Gene: SLCO1B7

Alternate names for this Gene:

Gene Summary:

Gene is located in Chromosome:

Location in Chromosome :

Description of this Gene:

Type of Gene:

rs4762694 in SLCO1B3-SLCO1B7;SLCO1B7 gene and Adolescent idiopathic scoliosis PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs11045627 in SLCO1B3-SLCO1B7;SLCO1B7 gene and Bilirubin level result PMID 19414484 2009 Genome-wide association meta-analysis for total serum bilirubin levels.

rs11045627 in SLCO1B3-SLCO1B7;SLCO1B7 gene and Bilirubin measurement PMID 19414484 2009 Genome-wide association meta-analysis for total serum bilirubin levels.

PMID 29403010 2018 Genetic analysis of quantitative traits in the Japanese population links cell types to complex human diseases.

rs4762694 in SLCO1B3-SLCO1B7;SLCO1B7 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3 PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.