About Us

Search Result


Gene id 6555
Gene Summary    Protein Summary    Gene ontology    KEGG pathways    Diseases    PubMed    

Gene Summary

Gene Symbol SLC10A2   Gene   UCSC   Ensembl
Aliases ASBT, IBAT, ISBT, NTCP2, PBAM
Gene name solute carrier family 10 member 2
Alternate names ileal sodium/bile acid cotransporter, Na(+)-dependent ileal bile acid transporter, ileal apical sodium-dependent bile acid transporter, ileal sodium-dependent bile acid transporter, sodium/taurocholate cotransporting polypeptide, ileal, solute carrier family 1,
Gene location 13q33.1 (103066416: 103043997)     Exons: 6     NC_000013.11
Gene summary(Entrez) This gene encodes a sodium/bile acid cotransporter. This transporter is the primary mechanism for uptake of intestinal bile acids by apical cells in the distal ileum. Bile acids are the catabolic product of cholesterol metabolism, so this protein is also
OMIM 609605

Protein Summary

Protein general information Q12908  

Name: Ileal sodium/bile acid cotransporter (Apical sodium dependent bile acid transporter) (ASBT) (Ileal Na(+)/bile acid cotransporter) (Ileal sodium dependent bile acid transporter) (IBAT) (ISBT) (Na(+) dependent ileal bile acid transporter) (Sodium/taurochola

Length: 348  Mass: 37714

Sequence MNDPNSCVDNATVCSGASCVVPESNFNNILSVVLSTVLTILLALVMFSMGCNVEIKKFLGHIKRPWGICVGFLCQ
FGIMPLTGFILSVAFDILPLQAVVVLIIGCCPGGTASNILAYWVDGDMDLSVSMTTCSTLLALGMMPLCLLIYTK
MWVDSGSIVIPYDNIGTSLVSLVVPVSIGMFVNHKWPQKAKIILKIGSIAGAILIVLIAVVGGILYQSAWIIAPK
LWIIGTIFPVAGYSLGFLLARIAGLPWYRCRTVAFETGMQNTQLCSTIVQLSFTPEELNVVFTFPLIYSIFQLAF
AAIFLGFYVAYKKCHGKNKAEIPESKENGTEPESSFYKANGGFQPDEK
Structural information
Interpro:  IPR002657  IPR004710  IPR038770  IPR030207  
STRING:   ENSP00000245312
Other Databases GeneCards:  SLC10A2  Malacards:  SLC10A2

Gene ontology

Expand All | Collapse All

GO accessionTerm nameEvidence codeGo category
GO:0016324 apical plasma membrane
IBA cellular component
GO:0008508 bile acid:sodium symporte
r activity
IBA molecular function
GO:0015721 bile acid and bile salt t
ransport
IBA biological process
GO:0008508 bile acid:sodium symporte
r activity
IEA molecular function
GO:0015721 bile acid and bile salt t
ransport
IEA biological process
GO:0016020 membrane
IEA cellular component
GO:0016021 integral component of mem
brane
IEA cellular component
GO:0016324 apical plasma membrane
IEA cellular component
GO:0006814 sodium ion transport
IEA biological process
GO:0016020 membrane
IEA cellular component
GO:0015293 symporter activity
IEA molecular function
GO:0016021 integral component of mem
brane
IEA cellular component
GO:0006811 ion transport
IEA biological process
GO:0008508 bile acid:sodium symporte
r activity
TAS molecular function
GO:0005886 plasma membrane
TAS cellular component
GO:0005887 integral component of pla
sma membrane
TAS cellular component
GO:0005886 plasma membrane
TAS cellular component
GO:0008508 bile acid:sodium symporte
r activity
TAS molecular function
GO:0015721 bile acid and bile salt t
ransport
TAS biological process
GO:0005515 protein binding
IPI molecular function
GO:0005515 protein binding
IPI molecular function
GO:0005515 protein binding
IPI molecular function
GO:0005515 protein binding
IPI molecular function
GO:0005515 protein binding
IPI molecular function
GO:0005515 protein binding
IPI molecular function
GO:0005515 protein binding
IPI molecular function
GO:0005515 protein binding
IPI molecular function
GO:0005515 protein binding
IPI molecular function
GO:0005515 protein binding
IPI molecular function
GO:0009617 response to bacterium
IEA biological process
GO:0005902 microvillus
IEA cellular component
GO:0016324 apical plasma membrane
IEA cellular component
GO:0016020 membrane
IEA cellular component
GO:0055085 transmembrane transport
IEA biological process

KEGG pathways

Expand All | Collapse All

Pathway idPathway name
hsa04976Bile secretion
Associated diseases References
Primary bile acid malabsorption KEGG:H01016
Primary bile acid malabsorption KEGG:H01016
Intestinal disease PMID:9109432
Spermatogenic defects MIK: 31037746

PubMed references

Expand All | Collapse All

PMID Condition Mutation Ethnicity Population details Infertility_type Associated_genes Abstract
31037746 Spermatoge
nic defect
s

16 (1 control,
15 cases)
Male infertility GSE6023 analyzed using GEO2R
Show abstract