SLC10A5 - solute carrier family 10 member 5 Gene

Also Known as P5

Species: Homo sapiens

Gene Type: protein coding
Gene ID: 347051

About SLC10A5

Cytogenetic location: 8q21.13 Genomic coordinates (GRCh38): 8:81,693,631-81,695,058 (from NCBI)

This gene has 1 transcript (splice variant), 65 orthologues and 5 paralogues.

Summary

Predicted to enable bile acid:sodium symporter activity. Predicted to be involved in bile acid and bile salt transport. Predicted to be integral component of membrane. [provided by Alliance of Genome Resources, Apr 2022]

SLC10A5 Products (1)

mRNA Protein Name
NM_001010893.3 NP_001010893.1 sodium/bile acid cotransporter 5 precursor

SLC10A5 Protein Structure

SBF

SBF: Sodium Bile acid symporter family (150 - 323)

  • 0
  • 100
  • 200
  • 300
  • 400
  • 438 a.a.
Protein Preferred Names Protein Names

sodium/bile acid cotransporter 5

  • Na(+)/bile acid cotransporter 5

Related Diseases

Diseases Alias
Dicarboxylic Aminoaciduria

  • Glutamate-Aspartate Transport Defect

  • Dicarboxylicaminoaciduria

  • DCBXA

  • Renal Aminoacidurias
Thiamine-Responsive Megaloblastic Anemia Syndrome

  • TRMA

  • Rogers Syndrome

  • Thiamine-Responsive Myelodysplasia

  • Thiamine-Responsive Anemia Syndrome

  • Thiamine Metabolism Dysfunction Syndrome 1

  • Thmd1

  • Megaloblastic Anemia, Thiamine-Responsive, With Diabetes Mellitus And Sensorineural Deafness

  • Thiamine-Responsive Megaloblastic Anemia With Diabetes Mellitus And Sensorineural Deafness

  • Thiamine Responsive Megaloblastic Anemia Syndrome

  • Megaloblastic Anemia Thiamine-Responsive With Diabetes Mellitus And Sensorineural Deafness

  • Thiamine-Responsive Megaloblastic Anemia

  • Thiamine-Responsive Anaemia Syndrome

  • Thiamine-Responsive Megaloblastic Anaemia Syndrome

  • Thiamine-Responsive Megaloblastic Anaemia With Diabetes Mellitus And Sensorineural Deafness

  • Thiamine-Responsive Megaloblastic Anemia With Diabetes Mellitus And Sensorineural Hearing Loss
Hydranencephaly

  • Hydroanencephaly
Benign Chronic Pemphigus

  • Hailey-Hailey Disease

  • Pemphigus, Benign Familial

  • Familial Benign Pemphigus

  • Benign Familial Pemphigus

  • Familial Benign Chronic Pemphigus

  • BCPM

  • HHD

  • Benign Chronic Familial Pemphigus Of Hailey-Hailey

  • Pemphigus, Chronic, Benign
Iminoglycinuria

  • Iminoglycinuria, Digenic

  • IG
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

Related Agents

  • Pre-clinical Phase

Pre-clinical Phase

Bioactive Molecules (1)
Cat. No. Product Name
Effect
Purity
Rare Diseases
HY-RS12991 SLC10A5 Human Pre-designed siRNA Set A Pre-designed Set / Unkown

Orthologs Information

Species Symbol Source ID
Mus musculus SLC10A5 MGD MGI:2685251
Bos taurus SLC10A5 VGNC VGNC:34662
Rattus norvegicus SLC10A5 RGD RGD:1306036
Macaca mulatta SLC10A5 VGNC VGNC:84115
Others SLC10A5 NCBI