SLCO1B3
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
- 12p12.2[14]
- Expressed in
- right lobe of liver, testicle, olfactory zone of nasal mucosa, Epithelium of choroid plexus, gonad, nasal epithelium, buccal mucosa cell, tibial nerve, canal of the cervix, gallbladder[15][16][17][18][19][20][21][22][23][24]
- Found in taxon
- Homo sapiens[10]
- Genetic association
- Rotor syndrome[12]
- HomoloGene ID
- 75119[3]
- Strand orientation
- forward strand[13]
🏷️ Also known as
en HBLRR
en LST-2
en LST3
en LST-3TM13
en OATP1B3
en OATP-8
en OATP8
en SLC21A8
en SLCO1B3
en solute carrier organic anion transporter family member 1B3
🔖 Identifiers · 10
- Ensembl gene ID
- ENSG00000111700
- Ensembl transcript ID
- ENST00000545880, ENST00000261196, ENST00000381545, ENST00000540853, ENST00000544370
- Entrez Gene ID
- 28234
- Exact match
- identifiers.org
- Freebase ID
- /m/03h056f
- HGNC ID
- 10961
- HGNC gene symbol
- SLCO1B3
- OMIM ID
- 605495
- RefSeq RNA ID
- NM_019844, NM_001349920
- UMLS CUI
- C1420132
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