2024年12月25日 · It encodes a protein which shows 97%, 85%, and 63% amino acid identity with mouse, chicken, and Xenopus Wnt11 protein, respectively. This gene may play roles in the development of skeleton, kidney and lung, and is considered to be a plausible candidate gene for High Bone Mass Syndrome.

2024年12月25日 · WNT1 (Wnt Family Member 1) is a Protein Coding gene. Diseases associated with WNT1 include Osteogenesis Imperfecta, Type Xv and Bone Mineral Density Quantitative Trait Locus 16.Among its related pathways are ncRNAs involved in Wnt signaling in hepatocellular carcinoma and Wnt Pathway.Gene Ontology (GO) annotations related to this gene include …

2024年12月25日 · WNT7B (Wnt Family Member 7B) is a Protein Coding gene. Diseases associated with WNT7B include Microphthalmia, Syndromic 9 and Macs Syndrome.Among its related pathways are ncRNAs involved in Wnt signaling in hepatocellular carcinoma and Wnt Pathway.Gene Ontology (GO) annotations related to this gene include signaling receptor …

Showing 25 of 5,735 results for WNT11 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 ...

2024年12月25日 · WNT5B (Wnt Family Member 5B) is a Protein Coding gene. Diseases associated with WNT5B include Type 1 Diabetes Mellitus 4 and Fibular Aplasia Or Hypoplasia, Femoral Bowing And Poly-, Syn-, And Oligodactyly.Among its related pathways are ncRNAs involved in Wnt signaling in hepatocellular carcinoma and Wnt Pathway.Gene Ontology (GO) …

2024年12月25日 · WNT5A (Wnt Family Member 5A) is a Protein Coding gene. Diseases associated with WNT5A include Robinow Syndrome, Autosomal Dominant 1 and Autosomal Dominant Robinow Syndrome.Among its related pathways are Autodegradation of the E3 ubiquitin ligase COP1 and ncRNAs involved in Wnt signaling in hepatocellular …

2024年12月25日 · WNT7A (Wnt Family Member 7A) is a Protein Coding gene. Diseases associated with WNT7A include Ulna And Fibula, Absence Of, With Severe Limb Deficiency and Fibular Aplasia Or Hypoplasia, Femoral Bowing And Poly-, Syn-, And Oligodactyly.Among its related pathways are ncRNAs involved in Wnt signaling in hepatocellular carcinoma and Wnt …

Complete information for lnc-WNT11-5 gene (RNA Gene), , including: function, proteins, disorders, pathways, orthologs, and expression. GeneCards - The Human Gene Compendium

2024年12月24日 · CTNNB1 (Catenin Beta 1) is a Protein Coding gene. Diseases associated with CTNNB1 include Pilomatrixoma and Colorectal Cancer.Among its related pathways are Signaling by GSK3beta mutants and Gastrulation.Gene Ontology (GO) annotations related to this gene include DNA-binding transcription factor activity and binding.An important paralog of this gene …

2024年12月25日 · FGFBP2 (Fibroblast Growth Factor Binding Protein 2) is a Protein Coding gene. Diseases associated with FGFBP2 include Asthma and Cervical Adenosquamous Carcinoma.Among its related pathways are Signaling by FGFR2 and Signal Transduction.Gene Ontology (GO) annotations related to this gene include growth factor binding.An important …