2025年3月30日 · TEC (Tec Protein Tyrosine Kinase) is a Protein Coding gene. Diseases associated with TEC include Transient Erythroblastopenia Of Childhood and Agammaglobulinemia . Among its related pathways are CD28 Signaling in T-Helper Cell and Cytokine Signaling in Immune system .

2025年3月30日 · TXK (TXK Tyrosine Kinase) is a Protein Coding gene. Diseases associated with TXK include Ulcer Of Anus And Rectum and Agammaglobulinemia. Among its related pathways are CD28 Signaling in T-Helper Cell and Innate Immune System.

2024年12月24日 · Complete information for ENSG00000279706 gene (Uncategorized), TEC, including: function, proteins, disorders, pathways, orthologs, and expression. GeneCards - The Human Gene Compendium

Symbol Description Category UniProt ID GIFtS GC id Score; 1: TEC: Tec Protein Tyrosine Kinase: Protein Coding: P42680: 57: GC04M048346: 85.71: 2: TXK: TXK Tyrosine Kinase

Complete information for ENSG00000280371 gene (Uncategorized), TEC Gene, including: function, proteins, disorders, pathways, orthologs, and expression. GeneCards - The Human Gene Compendium

2025年3月30日 · This protein is thought to participate in a positive feedback loop by upregulating the activity of tyrosine-protein kinase Tec. Variants of this gene have been associated with autosomal-dominant hypercholesterolemia (ADH), which is characterized by elevated low-density lipoprotein cholesterol levels and in increased risk of coronary vascular ...

2025年3月30日 · This gene encodes a non-receptor tyrosine kinase belonging to the Tec kinase family. The protein contains a PH-like domain, which mediates membrane targeting by binding to phosphatidylinositol 3,4,5-triphosphate (PIP3), and a SH2 domain that binds to tyrosine-phosphorylated proteins and functions in signal transduction.

2024年12月25日 · Complete information for lnc-TEC-2 gene (RNA Gene), , including: function, proteins, disorders, pathways, orthologs, and expression. GeneCards - The Human Gene Compendium

2025年3月30日 · NR4A3 (Nuclear Receptor Subfamily 4 Group A Member 3) is a Protein Coding gene. Diseases associated with NR4A3 include Chondrosarcoma, Extraskeletal Myxoid and Chondrosarcoma. Among its related pathways are Gene …

2025年3月30日 · The protein encoded by this gene plays a crucial role in B-cell development. Mutations in this gene cause X-linked agammaglobulinemia type 1, which is an immunodeficiency characterized by the failure to produce mature B lymphocytes, and associated with a failure of Ig heavy chain rearrangement.