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 |
|
Other Databases |
GeneCards: SLC10A2  Malacards: SLC10A2 |
|
GO accession | Term name | Evidence code | Go 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 |
|
|
Pathway id | Pathway name |
hsa04976 | Bile secretion | |
|
Associated diseases |
References |
Primary bile acid malabsorption | KEGG:H01016 |
Primary bile acid malabsorption | KEGG:H01016 |
Intestinal disease | PMID:9109432 |
Spermatogenic defects | MIK: 31037746 |
|
|
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 |
|