SLCO1B1
protein-coding gene in the species Homo sapiens
Facts
13 properties- Instance of
- gene
- Subclass of
- protein-coding gene
- Chromosome
- human chromosome 12[11]
- Cytogenetic location
- 12p12.1[14]
- Expressed in
- right lobe of liver, testicle, buccal mucosa cell, pancreatic ductal cell, gallbladder, renal cortex, cervix, canal of the cervix, mouth, haematopoietic system[15][16][17][18][19][20][21][22][23][24]
- Found in taxon
- Homo sapiens[10]
- Genetic association
- Rotor syndrome[12]
- HomoloGene ID
- 74575[3]
- Strand orientation
- forward strand[13]
🏷️ Also known as
en HBLRR
en LST-1
en LST1
en OATP1B1
en OATP2
en OATP-C
en OATPC
en SLC21A6
en SLCO1B1
en solute carrier organic anion transporter family member 1B1
🔖 Identifiers · 13
- OpenAlex ID
- C2776598434
- CIViC gene ID
- 8450
- Ensembl gene ID
- ENSG00000134538
- Ensembl transcript ID
- ENST00000256958
- Entrez Gene ID
- 10599
- Exact match
- identifiers.org
- Freebase ID
- /m/03gx65k
- HGNC ID
- 10959
- HGNC gene symbol
- SLCO1B1
- Microsoft Academic ID (discontinued)
- 2776598434
- OMIM ID
- 604843
- RefSeq RNA ID
- NM_006446
Show all 13 identifiers +1
- UMLS CUI
- C1420131
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