Basic Information
SLCO1B1
Full name: solute carrier organic anion transporter family member 1B1
Gene type: protein coding
HGNC ID: HGNC:10959
Gene location: 12p12.1
Gene resources
NCBI: https://www.ncbi.nlm.nih.gov/gene/10599
Alliance of genome: https://www.alliancegenome.org/gene/HGNC:10959
MANE select: https://www.ncbi.nlm.nih.gov/gene/?term=NM_006446.5
Protein resources
UniProt/Swiss-Prot: https://www.uniprot.org/uniprot/Q9Y6L6
AlphaFold: https://alphafold.ebi.ac.uk/entry/Q9Y6L6
MEME motif:
Clinical resources
Pathway resources
KEGG pathway: https://www.genome.jp/pathway/hsa04976+10599
Variant resources
Gene | Disease type | Variant type | NCBI dbSNP | Alleles | Variant location |
---|---|---|---|---|---|
SLCO1B1 | exudative AMD | Missense Variant | rs4149056 | T>C | chr12:21178615 (GRCh38.p13) |