Mar 30, 2025 · SLC10A2 (Solute Carrier Family 10 Member 2) is a Protein Coding gene. Diseases associated with SLC10A2 include Bile Acid Malabsorption, Primary, 1 and Progressive Familial Intrahepatic Cholestasis. Among its related pathways are Bile acid and bile salt metabolism and Metabolism.

Showing 25 of 2,997 results for SLC10A2 Search Time: 0 ms in Aliases & Descriptions Drugs & Compounds Disorders Text-Mined Disorders Domains Expression in Human Tissues Function Genomics Localization Orthologs Paralogs Pathways Phenotypes Proteins Publications Summaries Transcripts Variants in category Protein Coding RNA Gene Functional Element ...

Mar 30, 2025 · An important paralog of this gene is SLC10A2. UniProtKB/Swiss-Prot Summary for SLC10A6 Gene Transports sulfoconjugated steroid hormones from the extracellular compartment into the cytosol in a sodium-dependent manner without hydrolysis (PubMed: 17491011 , 23667501 , 24717977 , 28951227 ).

Mar 30, 2025 · SLC10A1 (Solute Carrier Family 10 Member 1) is a Protein Coding gene. Diseases associated with SLC10A1 include Hypercholanemia, Familial, 2 and Familial Hypercholanemia.Among its related pathways are Bile acid and bile salt metabolism and Metabolism.Gene Ontology (GO) annotations related to this gene include bile acid:sodium symporter activity and bile acid transmembrane transporter activity.

Mar 30, 2025 · SLC10A5 (Solute Carrier Family 10 Member 5) is a Protein Coding gene. Diseases associated with SLC10A5 include Dicarboxylic Aminoaciduria and Thiamine-Responsive Megaloblastic Anemia Syndrome.Gene Ontology (GO) annotations related to this gene include bile acid:sodium symporter activity.An important paralog of this gene is SLC10A3.

Dec 25, 2024 · Complete information for LINC01309 gene (RNA Gene), Long Intergenic Non-Protein Coding RNA 1309, including: function, proteins, disorders, pathways, orthologs, and expression. GeneCards - The Human Gene Compendium

Mar 30, 2025 · HSD3B7 (Hydroxy-Delta-5-Steroid Dehydrogenase, 3 Beta- And Steroid Delta-Isomerase 7) is a Protein Coding gene. Diseases associated with HSD3B7 include Bile Acid Synthesis Defect, Congenital, 1 and Congenital Bile Acid Synthesis Defect.Among its related pathways are Bile acid and bile salt metabolism and Metabolism.Gene Ontology (GO) annotations related to this gene include oxidoreductase ...

Complete information for lnc-SLC10A2-2 gene (RNA Gene), , including: function, proteins, disorders, pathways, orthologs, and expression. GeneCards - The Human Gene Compendium

Mar 30, 2025 · SLC10A4 (Solute Carrier Family 10 Member 4) is a Protein Coding gene. Gene Ontology (GO) annotations related to this gene include bile acid:sodium symporter activity.An important paralog of this gene is SLC10A2.

Mar 28, 2025 · ELOVL3 (ELOVL Fatty Acid Elongase 3) is a Protein Coding gene. Diseases associated with ELOVL3 include Spinocerebellar Ataxia 38 and Ichthyosis Vulgaris.Among its related pathways are docosahexaenoate biosynthesis III (mammals) and Transcriptional regulation of brown and beige adipocyte differentiation by EBF2.Gene Ontology (GO) annotations related to this gene include transferase activity.