The SLCO1B1 gene homepage

General information
Gene symbol SLCO1B1
Gene name solute carrier organic anion transporter family member 1B1
Chromosome 12
Chromosomal band p12.1
Imprinted Unknown
Genomic reference NG_011745.1
Transcript reference NM_006446.4
Associated with diseases Neonatal Hyperbilirubinemia
Citation reference(s) -
Curators (1) MyHVP
Total number of public variants reported 21
Unique public DNA variants reported 5
Individuals with public variants 5
Hidden variants -
Date created March 21, 2021
Date last updated August 01, 2021
Version SLCO1B1:210801

Graphical displays and utilities
Graphs Graphs displaying summary information of all variants in the database »
UCSC Genome Browser Show variants in the UCSC Genome Browser (full view, compact view)
Ensembl Genome Browser Show variants in the Ensembl Genome Browser (full view, compact view)
NCBI Sequence Viewer Show distribution histogram of variants in the NCBI Sequence Viewer

Links to other resources
HGNC 10959
Entrez Gene 10599
PubMed articles SLCO1B1
OMIM - Gene 604843
OMIM - Diseases Neonatal Hyperbilirubinemia
HGMD SLCO1B1
GeneCards SLCO1B1
GeneTests SLCO1B1


Active transcripts


ID     

Chr     

Name     

NCBI ID     

NCBI Protein ID     

DescendingVariants     
00000420 12 solute carrier organic anion transporter family member 1B1 NM_006446.4 NP_006437.3 21


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