SLC10A1 - solute carrier family 10 member 1 Gene

Also Known as NTCP; FHCA2

Species: Homo sapiens

Gene Type: protein coding
Gene ID: 6554

About SLC10A1

Cytogenetic location: 14q24.1 Genomic coordinates (GRCh38): 14:69,775,416-69,797,241 (from NCBI)

This gene has 1 transcript (splice variant), 265 orthologues, 5 paralogues and is associated with 1 phenotype. Restricted expression toward liver (RPKM 124.7).

Summary

The protein encoded by this gene belongs to the sodium/bile acid cotransporter family, which are integral membrane glycoproteins that participate in the enterohepatic circulation of bile acids. Two homologous transporters are involved in the reabsorption of bile acids; the ileal sodium/bile acid cotransporter with an apical cell localization that absorbs bile acids from the intestinal lumen, bile duct and kidney, and the liver-specific sodium/bile acid cotransporter, represented by this protein, that is found in the basolateral membranes of hepatocytes. Bile acids are the catabolic product of Cholesterol metabolism, hence this protein is important for Cholesterol homeostasis. [provided by RefSeq, Oct 2011]

SLC10A1 Products (1)

mRNA Protein Name
NM_003049.4 NP_003040.1 hepatic sodium/bile acid cotransporter
Molecular Function GO Annotation Evidence References Source
enables protein binding IPI
IPI: Inferred from physical interaction
32296183 GOA
EXP: Inferred from Experiment IDA: Inferred from direct assay IPI: Inferred from physical interaction IMP: Inferred from mutant phenotype IGI: Inferred from genetic interaction IEP: Inferred from expression pattern

SLC10A1 Protein Structure

SBF

SBF: Sodium Bile acid symporter family (33 - 212)

  • 0
  • 100
  • 200
  • 300
  • 349 a.a.
Protein Preferred Names Protein Names

hepatic sodium/bile acid cotransporter

  • Na(+)/bile acid cotransporter

SLC10A1 Protein-protein interaction Information

Type
Protein Name Protein ID Interactor Interactor Species Interactor ID Detection Method References
Intra
SLC10A1 Q14973 SLC25A46 Homo sapiens Q96AG3 32296183
Intra
SLC10A1 Q14973 SLC38A7 Homo sapiens Q9NVC3 32296183
Intra
SLC10A1 Q14973 TMEM242 Homo sapiens Q9NWH2 32296183
Intra
SLC10A1 Q14973 NINJ2 Homo sapiens Q9NZG7 32296183
Intra
SLC10A1 Q14973 ORMDL1 Homo sapiens Q9P0S3 32296183
Intra
SLC10A1 Q14973 TOMM6 Homo sapiens Q96B49 32296183
Intra
SLC10A1 Q14973 ORMDL2 Homo sapiens Q53FV1 32296183
Intra
SLC10A1 Q14973 FA2H Homo sapiens Q7L5A8 32296183
Intra
SLC10A1 Q14973 TVP23B Homo sapiens Q9NYZ1 32296183
Intra
SLC10A1 Q14973 TMEM239 Homo sapiens Q8WW34-2 32296183
Intra
SLC10A1 Q14973 CFHR5 Homo sapiens Q9BXR6 32296183
Intra
SLC10A1 Q14973 GPR151 Homo sapiens Q8TDV0 32296183
Intra
SLC10A1 Q14973 FAM241B Homo sapiens Q96D05-2 32296183
Intra
SLC10A1 Q14973 FAXDC2 Homo sapiens Q96IV6 32296183
Intra
SLC10A1 Q14973 TMEM121 Homo sapiens Q9BTD3 32296183
Intra
SLC10A1 Q14973 IFITM2 Homo sapiens Q6IBB0 32296183
Intra
SLC10A1 Q14973 TSPO2 Homo sapiens Q5TGU0 32296183
Intra
SLC10A1 Q14973 SLC16A13 Homo sapiens Q7RTY0 32296183
Intra
SLC10A1 Q14973 CLDN19 Homo sapiens Q8N6F1-2 32296183
Intra
SLC10A1 Q14973 PKMYT1 Homo sapiens Q99640-2 32296183
Intra
SLC10A1 Q14973 SLC41A1 Homo sapiens Q8IVJ1 32296183
Intra
SLC10A1 Q14973 DGAT2L6 Homo sapiens Q6ZPD8 32296183
Intra
SLC10A1 Q14973 OTOP3 Homo sapiens Q7RTS5 32296183
Intra
SLC10A1 Q14973 SLC12A7 Homo sapiens Q9Y666-2 32296183
Intra
SLC10A1 Q14973 SLC35E4 Homo sapiens Q6ICL7 32296183
Intra
SLC10A1 Q14973 SLC7A3 Homo sapiens Q8WY07 32296183
Intra
SLC10A1 Q14973 GPR152 Homo sapiens Q8TDT2 32296183
Intra
SLC10A1 Q14973 AGPAT3 Homo sapiens Q9NRZ7 32296183
Intra
SLC10A1 Q14973 ARL6IP6 Homo sapiens Q8N6S5 32296183
Intra
SLC10A1 Q14973 TMUB2 Homo sapiens Q71RG4 32296183
Intra
SLC10A1 Q14973 TMBIM1 Homo sapiens Q969X1 32296183
Intra
SLC10A1 Q14973 LRP10 Homo sapiens Q7Z4F1 32296183
Intra
SLC10A1 Q14973 GDE1 Homo sapiens Q9NZC3 32296183
Intra
SLC10A1 Q14973 COX20 Homo sapiens Q5RI15 32296183
Intra
SLC10A1 Q14973 TMEM60 Homo sapiens Q9H2L4 32296183
Intra
SLC10A1 Q14973 SFT2D1 Homo sapiens Q8WV19 32296183
Intra
SLC10A1 Q14973 q96fb2_human Homo sapiens Q96FB2 32296183
Intra
SLC10A1 Q14973 MFSD6 Homo sapiens Q6ZSS7 32296183
Intra
SLC10A1 Q14973 ACSL5 Homo sapiens Q9ULC5 32296183
Intra
SLC10A1 Q14973 TMEM222 Homo sapiens Q9H0R3 32296183
Intra
SLC10A1 Q14973 TMEM147 Homo sapiens Q9BVK8 32296183
Intra
SLC10A1 Q14973 SFXN1 Homo sapiens Q9H9B4 32296183
Intra
SLC10A1 Q14973 ATP6V0B Homo sapiens Q99437 32296183
Intra
SLC10A1 Q14973 SLC66A2 Homo sapiens Q8N2U9 32296183
Intra
SLC10A1 Q14973 SACM1L Homo sapiens Q9NTJ5 32296183
Intra
SLC10A1 Q14973 DERL1 Homo sapiens Q9BUN8 32296183
Intra
SLC10A1 Q14973 SCAMP4 Homo sapiens Q969E2 32296183
Intra
SLC10A1 Q14973 GIMAP5 Homo sapiens Q96F15 32296183
Intra
SLC10A1 Q14973 FXYD6 Homo sapiens Q9H0Q3 32296183
Intra
SLC10A1 Q14973 NEU1 Homo sapiens Q99519 32296183
Intra
SLC10A1 Q14973 ORMDL3 Homo sapiens Q8N138 32296183
Intra
SLC10A1 Q14973 VAMP3 Homo sapiens Q15836 32296183
Intra
SLC10A1 Q14973 CMTM3 Homo sapiens Q96MX0 32296183
Intra
SLC10A1 Q14973 YIPF6 Homo sapiens Q96EC8 32296183
Intra
SLC10A1 Q14973 YIPF4 Homo sapiens Q9BSR8 32296183
Intra
SLC10A1 Q14973 UNC50 Homo sapiens Q53HI1 32296183
Intra
SLC10A1 Q14973 RUSF1 Homo sapiens Q96GQ5 32296183
Intra
SLC10A1 Q14973 TMEM234 Homo sapiens Q8WY98 32296183
Intra
SLC10A1 Q14973 SELENOK Homo sapiens Q9Y6D0 32296183
Intra
SLC10A1 Q14973 PEX16 Homo sapiens Q9Y5Y5 32296183
Intra
SLC10A1 Q14973 SLC38A1 Homo sapiens Q9H2H9 32296183
Cross: Cross-species interaction Intra: Intraspecies interaction

SLC10A1 Antibodies

Cat. No. Product Name Application Reactivity
HY-P811318 NTCP Antibody WB, IHC-P, ICC/IF Human, Mouse, Rat

Related Diseases

Diseases Alias
Hypercholanemia, Familial, 2
  • FHCA2

  • Ntcp Deficiency

  • Hypercholanemia, Familial 2

  • Ntcpd

Hepatitis B
  • Chronic Hepatitis B

  • Hepatitis B Infection

  • Serum Hepatitis

  • HBV

  • Hepatitis B Chronic

  • Hbv, Susceptibility To

  • Hepatitis B, Chronic

  • Chronic Hepatitis B Without Delta Agent

  • Chronic Hbv - [Hepatitis B Virus] Infection

  • Hepatitis B Nos

  • Chronic Type B Viral Hepatitis

  • Hep B Nos

Biliary Atresia
  • Congenital Biliary Atresia

  • Isolated Biliary Atresia

  • Isolated Atresia Of Bile Ducts

  • Non-Syndromic Biliary Atresia

  • Atresia Of Bile Duct

  • Biliary Atresia, Congenital

  • Atresia Of Bile Ducts

  • Bile Duct Atresia

  • Congenital Bile Duct Atresia

  • Ba - [Biliary Atresia]

  • Impervious Bile Duct

  • Atresia Of Common Duct

  • Biliary Duct Atresia

  • Bile Ductal Atresia

  • Cystic Duct Atresia

Hepatitis
  • Chronic Hepatitis

  • Chronic Persistent Hepatitis

  • Acute Hepatitis

  • Hepatitis, Chronic

  • Acute And Subacute Liver Necrosis

  • Acute/Subac. Necrosis Of Liver

  • Animal Hepatitis

  • Hepatitis Chronic

  • Hepatitis A

  • Hepatitis, Animal

  • Hepatitis Due To Toxoplasmosis

  • Hepatitis In Toxoplasmosis

  • Toxoplasmal Hepatitis

  • Chronic Hepatitis, Unspecified

  • Chronic Active Hepatitis Nec

  • Other Specified Chronic Hepatitis

  • Chronic Persistent Hepatitis Nec

  • Chronic Lobular Hepatitis Nec

Cholestasis
  • Obstruction Of Bile Duct

  • Bile Duct Obstruction

  • Bile Occlusion

  • Extrahepatic Biliary Obstruction

  • Extrahepatic Bile Duct Obstruction

  • Bile Stasis

  • Biliary Stasis

  • Obstructive Hyperbilirubinemia

  • Obstructed Jaundice

  • Bile Duct Obstructed

  • Bile Ductal Obstruction

  • Biliary Duct Obstruction

  • Obstructed Bile Ductal

  • Obstructed Biliary Duct

  • Obstructed Biliary Ductal

  • Jaundice Regurgitation

  • Obstructive Jaundice

  • Cholestatic Jaundice

  • Cholestatic Jaundice Syndrome

Hepatoblastoma
Cholestasis, Benign Recurrent Intrahepatic, 1
  • Benign Recurrent Intrahepatic Cholestasis

  • BRIC1

  • Summerskill Syndrome

  • Bric

  • Summerskill-Walshe-Tygstrup Syndrome

  • Cholestasis, Benign Recurrent Intrahepatic

  • Benign Recurrent Intrahepatic Cholestasis 1

  • Benign Recurrent Intrahepatic Cholestasis Type 1

  • Bric Type 1

  • Low Gamma-Gt Familial Intrahepatic Cholestasis

  • Recurrent Familial Intrahepatic Cholestasis

  • Cholestasis, Benign Recurrent Intrahepatic 1

  • Mild Atp8b1 Deficiency

  • Recurrent Familial Intrahepatic Cholestasis 1

  • Abcb11-Related Intrahepatic Cholestasis

  • Atp8b1-Related Intrahepatic Cholestasis

  • Cholestasis, Intrahepatic, Recurrent, Benign, Type 1

  • Progressive Intrahepatic Cholestasis

  • Cholestasis, Progressive Familial Intrahepatic 3

  • Bric - [Benign Recurrent Intrahepatic Cholestasis]

Cholestasis, Progressive Familial Intrahepatic, 2
  • PFIC2

  • Cholestasis, Progressive Familial Intrahepatic 2

  • Progressive Familial Intrahepatic Cholestasis Type 2

  • Progressive Familial Intrahepatic Cholestasis 2

  • Bsep Deficiency

  • Recurrent Familial Intrahepatic Cholestasis 2

  • Benign Recurrent Intrahepatic Cholestasis 2

  • Severe Abcb11 Deficiency

  • Bric2

  • Cholestasis, Benign Recurrent Intrahepatic 2

  • Mild Abcb11 Deficiency

  • Cholestasis, Intrahepatic, Familial, Progressive, Type 2

Bile Acid Synthesis Defect, Congenital, 2
  • Cholestasis With Delta(4)-3-Oxosteroid 5-Beta-Reductase Deficiency

  • CBAS2

  • Congenital Bile Acid Synthesis Defect 2

  • Congenital Bile Acid Synthesis Defect Type 2

  • Congenital Bile Acid Synthesis Defect, Type 2

  • Basd2

  • Bile Acid Synthesis Defect, Congenital, Type 2

Pericholangitis
Intrahepatic Cholestasis Of Pregnancy
  • Recurrent Intrahepatic Cholestasis Of Pregnancy

  • Gravidic Intrahepatic Cholestasis

  • Pregnancy-Related Cholestasis

  • Icp

  • Pregnancy Related Cholestasis

  • Cholestasis, Intrahepatic Of Pregnancy

  • Familial Intrahepatic Cholestasis Of Pregnancy

  • Familial Recurrent Intrahepatic Cholestasis Of Pregnancy

  • Ricp

  • Obstetric Cholestasis

Liver Disease
  • Liver Failure

  • Liver Diseases

  • Abnormality Of The Liver

  • Liver Dysfunction

  • Disorder Of Liver

  • Hepatic Disorder

  • Hepatic Disease

  • Disease Of Bilirubin Metabolism

  • Disorder Of Bilirubin Metabolism

  • Liver Decompensation

  • Liver Function Failure

  • Hepatic Failure Nos

  • Liver Failure Nos

  • End Stage Liver Disease

  • Decompensated Liver Failure

  • Decompensation Of Liver Function

  • Hepatic Decompensation

  • Hepatic Insufficiency

  • Liver Cell Necrosis With Hepatic Failure

  • Liver Insufficiency

  • Decompensated Liver Disease

  • End Stage Liver Failure

  • Liver Necrosis With Hepatic Failure

Hepatitis D
  • Delta Hepatitis

  • Hepatitis Delta

  • Hdv

  • Hepatitis D Virus

  • Hepatitis D Infection

Progressive Familial Intrahepatic Cholestasis
  • Abcb4-Related Intrahepatic Cholestasis

  • Cholestasis, Progressive Familial Intrahepatic

  • Pfic

  • Byler Disease

  • Abcb11-Related Intrahepatic Cholestasis

  • Atp8b1-Related Intrahepatic Cholestasis

  • Bsep Deficiency

  • Byler Disease

  • Byler Syndrome

  • Fic1 Deficiency

  • Low Γ-Gt Familial Intrahepatic Cholestasis

  • Mdr3 Deficiency

  • Pfic

  • Cholestasis, Intrahepatic, Familial, Progressive

  • Pfic - [Progressive Familial Intrahepatic Cholestasis]

Cholestasis, Progressive Familial Intrahepatic, 3
  • PFIC3

  • Cholestasis, Progressive Familial Intrahepatic 3

  • Mdr3 Deficiency

  • Progressive Familial Intrahepatic Cholestasis Type 3

  • Progressive Familial Intrahepatic Cholestasis 3

  • Progressive Familial Intrahepatic Cholestasis With Elevated Serum Gamma-Glutamyltransferase

  • Cholestasis, Progressive Familial Intrahepatic, With Elevated Serum Gamma-Glutamyltransferase

  • Progressive Familial Intrahepatic Cholestasis With Elevated Serum Gama-Glutamyltransferase

  • Cholestasis, Intrahepatic, Familial, Progressive, Type 3

Extrahepatic Cholestasis
  • Cholestasis, Extrahepatic

  • Extrahepatic Biliary Stasis

  • Extrahepatic Obstructive Biliary Disease

  • Cholestasis Extrahepatic

Non-Alcoholic Fatty Liver Disease
  • Fatty Liver

  • Non-Alcoholic Fatty Liver

  • Nafld

  • Nonalcoholic Fatty Liver Disease

  • Nonalcoholic Steatohepatitis

  • Steatosis

  • Nafl

  • Nash

  • Non-Alcoholic Steatohepatitis

  • Susceptibility To Nonalcoholic Fatty Liver Disease

  • Steatohepatitis

  • Fatty Degeneration

  • Non-Alcoholic Fatty Liver Disease Without Mention Of Non-Alcoholic Steatohepatitis

  • Nafld Without Nash

  • Nafld Without Mention Of Nash

Cholestasis, Progressive Familial Intrahepatic, 1
  • PFIC1

  • Byler Disease

  • Cholestasis, Progressive Familial Intrahepatic 1

  • Progressive Familial Intrahepatic Cholestasis 1

  • Progressive Familial Intrahepatic Cholestasis Type 1

  • Fic1 Deficiency

  • Byler'S Disease

  • Cholestasis, Fatal Intrahepatic

  • Progressive Familial Intrahepatic Cholestasis

  • Severe Atp8b1 Deficiency

  • Fatal Intrahepatic Cholestasis

  • Cholestasis, Intrahepatic, Familial, Progressive, Type 1

  • Progressive Intrahepatic Cholestasis

  • Cholestasis, Progressive Familial Intrahepatic 3

Hard Palate Cancer
  • Malignant Neoplasm Of Hard Palate

  • Malignant Tumor Of Hard Palate

  • Malignant Tumour Of Hard Palate

Bile Duct Disease
  • Bile Duct Diseases

  • Bile Duct Disorder

  • Disorder Of Bile Duct

Biliary Tract Disease
  • Biliary Tract Diseases

  • Biliary Tract Abnormality

Sclerosing Cholangitis
  • Fibrosing Cholangitis

  • Cholangitis, Sclerosing

  • Primary Sclerosing Cholangitis

Bilirubin Metabolic Disorder
  • Hyperbilirubinemia

  • Hereditary Hyperbilirubinemia

  • Hyperbilirubinemia, Hereditary

  • Hyperbilirubinaemia

Cholangitis, Primary Sclerosing
  • Primary Sclerosing Cholangitis

  • PSC

  • Sclerosing Cholangitis

  • Cholangitis, Sclerosing

  • Cholangitis Primary Sclerosing

  • Psc - [Primary Sclerosing Cholangitis]

Primary Biliary Cholangitis
  • Primary Biliary Cirrhosis

  • Biliary Liver Cirrhosis

  • Chronic Nonsuppurative Destructive Cholangitis

  • Familial Primary Biliary Cirrhosis

  • Pbc

  • Hanot Syndrome

  • Cholestatic Cirrhosis

  • Biliary Cirrhosis Primary

  • Liver Cirrhosis, Biliary

  • Hanot'S Cirrhosis

  • Biliary Cirrhosis

  • Pericholangiolic Biliary Cirrhosis

  • Tannhauser-Magendantz Syndrome

  • Hanot-Rossle Syndrome

  • Hypertrophic Cirrhosis

  • Todd Cirrhosis

  • Hanot Cirrhosis

  • Charcot Cirrhosis

  • Mahon-Tannhauser Syndrome

  • Toxic Cirrhosis

  • Hypertrophic Biliary Cirrhosis

  • Monolobular Cirrhosis

  • Unilobar Cirrhosis

  • Xanthomatous Biliary Cirrhosis

Diseases Alias
Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Orthologs Information

Species Symbol Source ID
Felis catus SLC10A1 VGNC VGNC:65180
Bos taurus SLC10A1 VGNC VGNC:34659
Canis familiaris SLC10A1 VGNC VGNC:46211
Rattus norvegicus SLC10A1 RGD RGD:3681
Macaca mulatta SLC10A1 VGNC VGNC:77380
Mus musculus SLC10A1 MGD MGI:97379
Others SLC10A1 NCBI