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- Advanced Search - GeneCards
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- MECP2 Gene - GeneCards | MECP2 Protein | MECP2 Antibody
GeneCards Summary for MECP2 Gene MECP2 (Methyl-CpG Binding Protein 2) is a Protein Coding gene Diseases associated with MECP2 include Rett Syndrome and Encephalopathy, Neonatal Severe, Due To Mecp2 Mutations Among its related pathways are Transcriptional Regulation by MECP2 and Disorders of Nervous System Development
- VHL Gene - GeneCards | VHL Protein | VHL Antibody
Summaries for VHL Gene NCBI Gene Summary for VHL Gene This gene encodes a component of a ubiquitination complex The encoded protein is involved in the ubiquitination and degradation of hypoxia-inducible-factor (HIF), which is a transcription factor that plays a central role in the regulation of gene expression by oxygen
- ERBB2 Gene - GeneCards | ERBB2 Protein | ERBB2 Antibody
Gene Ontology (GO) annotations related to this gene include identical protein bindingand protein kinase activity An important paralog of this gene is EGFR UniProtKB Swiss-Prot Summary for ERBB2 Gene Protein tyrosine kinase that is part of several cell surface receptor complexes, but that apparently needs a coreceptor for ligand binding
- FOXP3 Gene - GeneCards | FOXP3 Protein | FOXP3 Antibody
Summaries for FOXP3 Gene NCBI Gene Summary for FOXP3 Gene The protein encoded by this gene is a member of the forkhead winged-helix family of transcriptional regulators Defects in this gene are the cause of immunodeficiency polyendocrinopathy, enteropathy, X-linked syndrome (IPEX), also known as X-linked autoimmunity-immunodeficiency syndrome
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