Mar 30, 2025 · SLC26A2 (Solute Carrier Family 26 Member 2) is a Protein Coding gene. Diseases associated with SLC26A2 include Achondrogenesis, Type Ib and Atelosteogenesis, Type Ii. Among its related pathways are Transport of inorganic cations/anions and amino acids/oligopeptides and Cytosolic sulfonation of small molecules.

Mar 30, 2025 · An important paralog of this gene is SLC26A2. UniProtKB/Swiss-Prot Summary for SLC26A1 Gene Sodium-independent sulfate anion transporter (PubMed: 12713736 , 27125215 ).

Mar 30, 2025 · SLC26A3 (Solute Carrier Family 26 Member 3) is a Protein Coding gene. Diseases associated with SLC26A3 include Diarrhea 1, Secretory Chloride, Congenital and Intestinal Obstruction.Among its related pathways are Transport of inorganic cations/anions and amino acids/oligopeptides and Disorders of transmembrane transporters.Gene Ontology (GO) annotations related to this gene include DNA-binding ...

Mar 30, 2025 · SLC26A5 (Solute Carrier Family 26 Member 5) is a Protein Coding gene. Diseases associated with SLC26A5 include Deafness, Autosomal Recessive 61 and Rare Autosomal Recessive Non-Syndromic Sensorineural Deafness Type Dfnb.Among its related pathways are Sensory processing of sound and Olfactory Signaling Pathway.Gene Ontology (GO) annotations related to this gene include spectrin binding and ...

Mar 30, 2025 · SLC6A2 (Solute Carrier Family 6 Member 2) is a Protein Coding gene. Diseases associated with SLC6A2 include Orthostatic Intolerance and Oppositional Defiant Disorder.Among its related pathways are Transport of inorganic cations/anions and amino acids/oligopeptides and Disorders of transmembrane transporters.Gene Ontology (GO) annotations related to this gene include beta-tubulin binding and ...

Mar 30, 2025 · SLC26A6 (Solute Carrier Family 26 Member 6) is a Protein Coding gene. Diseases associated with SLC26A6 include Bardet-Biedl Syndrome and Nephrolithiasis.Among its related pathways are Transport of inorganic cations/anions and amino acids/oligopeptides and Proximal tubule transport.Gene Ontology (GO) annotations related to this gene include PDZ domain binding and secondary active sulfate ...

Mar 30, 2025 · Exhibits sodium-independent sulfate anion transporter activity that may cooperate with SLC26A2 to mediate DIDS-sensitive sulfate uptake into high endothelial venules endothelial cells (HEVEC) (PubMed:12626430).

Mar 30, 2025 · SLC26A7 (Solute Carrier Family 26 Member 7) is a Protein Coding gene. Diseases associated with SLC26A7 include Allan-Herndon-Dudley Syndrome and Congenital Hypothyroidism.Among its related pathways is Transport of inorganic cations/anions and amino acids/oligopeptides.Gene Ontology (GO) annotations related to this gene include chloride channel activity and sulfate transmembrane transporter ...

Mar 30, 2025 · SLC26A9 (Solute Carrier Family 26 Member 9) is a Protein Coding gene. Diseases associated with SLC26A9 include Pancreatitis and Ileus.Among its related pathways is Transport of inorganic cations/anions and amino acids/oligopeptides.Gene Ontology (GO) annotations related to this gene include chloride channel activity and secondary active sulfate transmembrane transporter activity.

Mar 30, 2025 · SLC26A4 (Solute Carrier Family 26 Member 4) is a Protein Coding gene. Diseases associated with SLC26A4 include Pendred Syndrome and Deafness, Autosomal Recessive 4, With Enlarged Vestibular Aqueduct.Among its related pathways are Transport of inorganic cations/anions and amino acids/oligopeptides and Disorders of transmembrane transporters.Gene Ontology (GO) annotations related to this gene ...