Mar 30, 2025 · SLC4A11 (Solute Carrier Family 4 Member 11) is a Protein Coding gene. Diseases associated with SLC4A11 include Corneal Endothelial Dystrophy and Corneal Dystrophy And Perceptive Deafness . Gene Ontology (GO) annotations related to this gene include transporter activity and symporter activity .

Showing 25 of 1,389 results for SLC4A11 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 · SLC4A10 (Solute Carrier Family 4 Member 10) is a Protein Coding gene. Diseases associated with SLC4A10 include Neurodevelopmental Disorder With Hypotonia And Characteristic Brain Abnormalities and Complex Partial Epilepsy.Among its related pathways is Transport of inorganic cations/anions and amino acids/oligopeptides.Gene Ontology (GO) annotations related to this gene include transporter ...

Complete information for lnc-SLC4A11-3 gene (RNA Gene), , including: function, proteins, disorders, pathways, orthologs, and expression. GeneCards - The Human Gene Compendium

Mar 30, 2025 · SLC4A1 (Solute Carrier Family 4 Member 1 (Diego Blood Group)) is a Protein Coding gene. Diseases associated with SLC4A1 include Renal Tubular Acidosis, Distal, 1 and Cryohydrocytosis.Among its related pathways are Transport of inorganic cations/anions and amino acids/oligopeptides and Erythrocytes take up carbon dioxide and release oxygen.Gene Ontology (GO) annotations related to this gene ...

Mar 30, 2025 · SLC7A11 (Solute Carrier Family 7 Member 11) is a Protein Coding gene. Diseases associated with SLC7A11 include Lysinuric Protein Intolerance and Brain Edema.Among its related pathways are Nuclear events mediated by NFE2L2 and Transport of inorganic cations/anions and amino acids/oligopeptides.Gene Ontology (GO) annotations related to this gene include amino acid transmembrane transporter ...

Mar 30, 2025 · UNC5B (Unc-5 Netrin Receptor B) is a Protein Coding gene. Diseases associated with UNC5B include Hyperinsulinemic Hypoglycemia, Familial, 3 and Epilepsy.Among its related pathways are Nervous system development and Netrin-1 signaling.An important paralog of this gene is UNC5C.

Mar 30, 2025 · SLC5A11 (Solute Carrier Family 5 Member 11) is a Protein Coding gene. Diseases associated with SLC5A11 include Lupus Erythematosus.Among its related pathways are Transport of inorganic cations/anions and amino acids/oligopeptides and Nuclear receptors meta-pathway.Gene Ontology (GO) annotations related to this gene include transporter activity and symporter activity.

Mar 30, 2025 · SLC4A4 (Solute Carrier Family 4 Member 4) is a Protein Coding gene. Diseases associated with SLC4A4 include Proximal Renal Tubular Acidosis-Ocular Anomaly Syndrome and Renal Tubular Acidosis.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 ...

Mar 30, 2025 · SLC4A3 (Solute Carrier Family 4 Member 3) is a Protein Coding gene. Diseases associated with SLC4A3 include Short Qt Syndrome 7 and Familial Short Qt Syndrome.Among its related pathways are Transport of inorganic cations/anions and amino acids/oligopeptides and Hepatic ABC Transporters.Gene Ontology (GO) annotations related to this gene include transporter activity and monoatomic anion ...