Mar 30, 2025 · CCN3 (Cellular Communication Network Factor 3) is a Protein Coding gene. Diseases associated with CCN3 include Long Qt Syndrome and Wilms Tumor 5 . Among its related pathways are G-protein signaling G-Protein alpha-i signaling cascades and Adhesion .

Mar 30, 2025 · CCN2 (Cellular Communication Network Factor 2) is a Protein Coding gene. Diseases associated with CCN2 include Spondyloepimetaphyseal Dysplasia, Li-Shao-Li Type and Kyphomelic Dysplasia. Among its related pathways are Apoptotic Pathways in Synovial Fibroblasts and GPCR Pathway. An important paralog of this gene is CCN3.

Mar 30, 2025 · NCBI Gene Summary for CCNJL Gene Predicted to enable cyclin-dependent protein serine/threonine kinase regulator activity. Predicted to be involved in G1/S transition of mitotic cell cycle.

Dec 24, 2024 · CNN3 (Calponin 3) is a Protein Coding gene. Gene Ontology (GO) annotations related to this gene include actin binding and calmodulin binding. An important paralog of this gene is CNN2.

Mar 28, 2025 · CLCN3 (Chloride Voltage-Gated Channel 3) is a Protein Coding gene. Diseases associated with CLCN3 include Neurodevelopmental Disorder With Seizures And Brain Abnormalities and Neurodevelopmental Disorder With Hypotonia And Brain Abnormalities. Among its related pathways are Activation of cAMP-Dependent PKA and Ion channel transport.

Mar 30, 2025 · CCN4 (Cellular Communication Network Factor 4) is a Protein Coding gene. Diseases associated with CCN4 include Colorectal Cancer and Hepatocellular Carcinoma. An important paralog of this gene is CCN6.

Showing 25 of 940 results for CCN3 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 · CCND1 (Cyclin D1) is a Protein Coding gene. Diseases associated with CCND1 include Von Hippel-Lindau Syndrome and Myeloma, Multiple. Among its related pathways are Defective binding of RB1 mutants to E2F1,(E2F2, E2F3) and Autodegradation of …

Mar 30, 2025 · FBLN1 (Fibulin 1) is a Protein Coding gene. Diseases associated with FBLN1 include Synpolydactyly 2 and Fbln1-Related Developmental Delay-Central Nervous System Anomaly-Syndactyly Syndrome. Among its related pathways are Elastic fibre formation and Extracellular matrix organization.

Mar 30, 2025 · Complete information for FERRY3 gene (Protein Coding), FERRY Endosomal RAB5 Effector Complex Subunit 3, including: function, proteins, disorders, pathways, orthologs, and expression. GeneCards - The Human Gene Compendium