Gene Gene information from NCBI Gene database.
Entrez ID 123264
Gene name SLC51 subunit beta
Gene symbol SLC51B
Synonyms (NCBI Gene)
OSTBOSTBETAPBAM2SLC51A1BP
Chromosome 15
Chromosome location 15q22.31
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
32
GO ID Ontology Definition Evidence Reference
GO:0005515 Function Protein binding IPI 32296183
GO:0005886 Component Plasma membrane IDA 12719432
GO:0005886 Component Plasma membrane IEA
GO:0005886 Component Plasma membrane TAS
GO:0006869 Process Lipid transport IEA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
612085 29956 ENSG00000186198
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q86UW2
Protein name Organic solute transporter subunit beta (OST-beta) (Solute carrier family 51 subunit beta)
Protein function Essential component of the Ost-alpha/Ost-beta complex, a heterodimer that acts as the intestinal basolateral transporter responsible for bile acid export from enterocytes into portal blood (PubMed:16317684). Modulates SLC51A glycosylation, membr
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF15048 OSTbeta 3 122 Organic solute transporter subunit beta protein Family
Tissue specificity TISSUE SPECIFICITY: Widely expressed with a high expression in ileum. Expressed in testis, colon, liver, small intestine, kidney, ovary and adrenal gland; and at low levels in heart, lung, brain, pituitary, thyroid gland, uterus, prostate, mammary gland a
Sequence
Sequence length 128
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  KEGG 
  Bile secretion  
Associated diseases Disease associations from ClinVar categorized as Causal (Pathogenic/Likely Pathogenic) or Unknown.
12
Causal Diseases associated with Pathogenic or Likely Pathogenic variants in ClinVar
Phenotype Name Clinical Significance dbSNP ID RCV Accession
Bile acid malabsorption, primary, 2 Likely pathogenic rs1595900104 RCV001563707
Cholestasis Likely pathogenic rs1595900104 RCV000991455
Diarrhea Likely pathogenic rs1595900104 RCV000991455
Unknown Diseases with uncertain, conflicting, or no pathogenic evidence in ClinVar
Phenotype Name Clinical Significance dbSNP ID RCV Accession
Lung cancer Likely benign rs376773798 RCV005930321
SLC51B-related disorder Likely benign; Uncertain significance rs752749624, rs147682812, rs142436732, rs150408669, rs776892359, rs2506191524, rs749508267, rs2506182762 RCV003900953
RCV004757548
RCV003961320
RCV003916684
RCV004757603
RCV003982732
RCV003899148
RCV003969126
Associations from Text MiningDisease associations identified through Pubtator
Disease Name Relationship Type References
Bile Acid Malabsorption Primary Associate 28898457
Carcinoma Hepatocellular Associate 34128989, 35592684
Chemical and Drug Induced Liver Injury Associate 29420067, 34599072
Cholangitis Sclerosing Associate 28008998
Cholelithiasis Associate 18469300
Cholestasis Associate 25798860, 29420067, 34599072
Diarrhea Associate 28898457
Endometrial Neoplasms Inhibit 33917029
Gallstones Associate 18469300
Liver Cirrhosis Biliary Associate 29420067