Nov 10, 2025 · The knowledgebase automatically integrates gene-centric data from ~200 web sources, including genomic, transcriptomic, proteomic, genetic, clinical and functional information.

Nov 14, 2025 · This gene is one of two neighboring gene family members that encode mitochondrial enzymes which catalyze the oxidative deamination of amines, such as dopamine, norepinephrine, …

Nov 14, 2025 · LRRK2 (Leucine Rich Repeat Kinase 2) is a Protein Coding gene. Diseases associated with LRRK2 include Parkinson Disease 8, Autosomal Dominant and Parkinson's Disease.

Nov 14, 2025 · This gene encodes the human homolog of the mouse p (pink-eyed dilution) gene. The encoded protein is believed to be an integral membrane protein involved in small molecule transport, …

Nov 13, 2025 · HBB (Hemoglobin Subunit Beta) is a Protein Coding gene. Diseases associated with HBB include Sickle Cell Disease and Beta-Thalassemia, Dominant Inclusion Body Type.

Nov 13, 2025 · Complete information for CFH gene (Protein Coding), Complement Factor H, including: function, proteins, disorders, pathways, orthologs, and expression. GeneCards - The Human Gene …

Nov 14, 2025 · The protein encoded by this gene is a serine protease inhibitor belonging to the serpin superfamily whose targets include elastase, plasmin, thrombin, trypsin, chymotrypsin, and …

Nov 14, 2025 · LTC4S (Leukotriene C4 Synthase) is a Protein Coding gene. Diseases associated with LTC4S include Leukotriene C4 Synthase Deficiency and Aspirin-Induced Respiratory Disease.

Nov 13, 2025 · Complete information for GRIN2A gene (Protein Coding), Glutamate Ionotropic Receptor NMDA Type Subunit 2A, including: function, proteins, disorders, pathways, orthologs, and expression.

Nov 13, 2025 · A missense mutation in this gene causes myoclonus dystonia; other mutations have been associated with schizophrenia. Alternative splicing of this gene results in two transcript variants …