Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
123264
Gene name Gene Name - the full gene name approved by the HGNC.
SLC51 subunit beta
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
SLC51B
Synonyms (NCBI Gene) Gene synonyms aliases
OSTB, OSTBETA, PBAM2, SLC51A1BP
Disease Acronyms (UniProt) Disease acronyms from UniProt database
PBAM2
Chromosome Chromosome number
15
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
15q22.31
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0005215 Function Transporter activity IBA 21873635
GO:0005515 Function Protein binding IPI 32296183
GO:0005886 Component Plasma membrane IBA 21873635
GO:0005886 Component Plasma membrane IDA 12719432
GO:0015125 Function Bile acid transmembrane transporter activity IEA
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
612085 29956 ENSG00000186198
Protein
UniProt ID 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 information provided by ClinVar, GenCC, and GWAS databases.
Causal
Disease term Disease name dbSNP ID References
Cholestasis Cholestasis rs121909103, rs751511532, rs376368459, rs762702807, rs1578490102, rs1578499691, rs1578504946, rs1317656688, rs199791850, rs1452792080, rs1578491039 16423920, 22461449
Unknown
Disease term Disease name Evidence References Source
Bile Acid Malabsorption bile acid malabsorption, primary, 2 GenCC
Associations from Text Mining
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