2024年12月24日 · EGLN2 (Egl-9 Family Hypoxia Inducible Factor 2) is a Protein Coding gene. Diseases associated with EGLN2 include Pheochromocytoma and Polycythemia. Among its related pathways are Cellular responses to stimuli and …

2024年12月25日 · RAB4B-EGLN2 (RAB4B-EGLN2 Readthrough (NMD Candidate)) is an RNA Gene, and is affiliated with the ncRNA class. Diseases associated with RAB4B-EGLN2 include Hepatocellular Carcinoma. Gene Ontology (GO) annotations related to this gene include GTP binding and GTPase activity.

2024年12月24日 · EGLN3 (Egl-9 Family Hypoxia Inducible Factor 3) is a Protein Coding gene. Diseases associated with EGLN3 include Pheochromocytoma and Renal Cell Carcinoma.Among its related pathways are Cellular responses to stimuli and Autodegradation of the E3 ubiquitin ligase COP1.Gene Ontology (GO) annotations related to this gene include oxidoreductase …

Showing 25 of 2,728 results for EGLN2 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24日 · An important paralog of this gene is EGLN2. UniProtKB/Swiss-Prot Summary for EGLN1 Gene Cellular oxygen sensor that catalyzes, under normoxic conditions, the post-translational formation of 4-hydroxyproline in hypoxia-inducible factor (HIF) alpha proteins.

2024年12月25日 · WNT10A (Wnt Family Member 10A) is a Protein Coding gene. Diseases associated with WNT10A include Schopf-Schulz-Passarge Syndrome and Odontoonychodermal Dysplasia.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 …

Complete information for lnc-EGLN2-2 gene (RNA Gene), , including: function, proteins, disorders, pathways, orthologs, and expression. GeneCards - The Human Gene Compendium

2024年12月25日 · RAB4B HSALNG0126141 RAB4B-EGLN2 ENSG00000282951 EGLN2 MIA-RAB4B: GH19J040747: Promoter/Enhancer: 2.6 : RefSeq EPDnew FANTOM5 Ensembl ENCODE CraniofacialAtlas dbSUPER: 12.20: 31.77-25.5: 6: 9.8: KLF6 SP1 MIER1 MGA HDAC2 ZBTB26 SIX5 POLR2A KLF17 PRDM1:

2024年12月25日 · In normoxia, is hydroxylated on Pro-402 and Pro-564 in the oxygen-dependent degradation domain (ODD) by EGLN1/PHD2 and EGLN2/PHD1 (PubMed:11292861, 11566883, 12351678, 15776016, 25974097). EGLN3/PHD3 has also been shown to hydroxylate Pro-564 (PubMed: 11292861 , 11566883 , 12351678 , 15776016 , 25974097 ).

Symbol Description Category UniProt ID GIFtS GC id Score; 1: CHURC1-FNTB: CHURC1-FNTB Readthrough: Protein Coding: 25: GC14P064914: 52.30: 2: ENSG00000272158: Novel Transcript, Antisense To CHURC1-FNTB