2025年3月28日 · GeneCards is a searchable, integrative database that provides comprehensive, user-friendly information on all annotated and predicted human genes. The knowledgebase automatically integrates gene-centric data from ~200 web sources, including genomic, transcriptomic, proteomic, genetic, clinical and functional information.

genecards suite products are for research use only, do not provide medical advice and are not for use in diagnostic procedures.

GeneAnalytics enables researchers to identify compounds related to their gene sets, and further link to biochemical and pharmacological information about drugs, small molecules and metabolites, their mechanisms of action and their targets.

2025年3月30日 · WAS (WASP Actin Nucleation Promoting Factor) is a Protein Coding gene. Diseases associated with WAS include Wiskott-Aldrich Syndrome and Neutropenia, Severe Congenital, X-Linked. Among its related pathways are Regulation of actin dynamics for phagocytic cup formation and Signaling by Rho GTPases.

2025年3月28日 · Complete information for CTNNB1 gene (Protein Coding), Catenin Beta 1, including: function, proteins, disorders, pathways, orthologs, and expression. GeneCards - The Human Gene Compendium

GeneCards® is an integrated database of human genes that includes automatically-mined genomic, proteomic and transcriptomic information, as well as orthologies, disease relationships, SNPs, gene expression, gene function, and links for ordering assays and antibodies.

2025年3月30日 · This gene encodes the pro-alpha1 chains of type I collagen whose triple helix comprises two alpha1 chains and one alpha2 chain. Type I is a fibril-forming collagen found in most connective tissues and is abundant in bone, cornea, dermis and tendon.

2025年3月30日 · 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 plasminogen activator.

GeneAnalytics™ – GeneAnalytics supports analysis of gene sets with multiple genes, and enables matching of gene sets to tissues and cells within LifeMap Discovery.

2025年3月30日 · XDH (Xanthine Dehydrogenase) is a Protein Coding gene. Diseases associated with XDH include Xanthinuria, Type I and Xanthinuria, Type Ii. Among its related pathways are Metabolism of nucleotides and urate biosynthesis/inosine 5'-phosphate degradation.