2024年12月24日 · EIF1B (Eukaryotic Translation Initiation Factor 1B) is a Protein Coding gene. Diseases associated with EIF1B include Mixed Cell Uveal Melanoma and Choroid Cancer. Gene Ontology (GO) annotations related to this gene include RNA binding and translation initiation factor activity. An important paralog of this gene is EIF1.

Eukaryotic translation initiation factor 1b is a protein that in humans is encoded by the EIF1B gene. [5] [6]

关于 eif1b This gene has 4 transcripts (splice variants), 158 orthologues and 1 paralogue. Ubiquitous expression in heart (RPKM 113.1), bone marrow (RPKM 72.6) and 25 other tissues.

2024年6月17日 · Enables RNA binding activity. Predicted to be involved in translational initiation. Predicted to be part of eukaryotic 43S preinitiation complex. [provided by Alliance of Genome Resources, Apr 2022] Go to reference sequence details. Go to …

2025年2月8日 · eukaryotic translation initiation factor 1b, protein translation factor SUI1 homolog GC20, translation factor sui1 homolog. Enables RNA binding activity. Predicted to be involved in regulation of translational initiation. Predicted to be part of eukaryotic 43S preinitiation complex. [provided by Alliance of Genome Resources, Feb 2025]

2023年11月23日 · EIF1B eukaryotic translation initiation factor 1B Gene ID: 10289, updated on 23-Nov-2023 Gene type: protein coding Also known as: GC20. See all available tests in GTR for this gene; Go to complete Gene record for EIF1B; Go to Variation Viewer for EIF1B variants; Summary. Enables RNA binding activity.

Human Gene EIF1B (ENST00000232905.4) from GENCODE V44 Description: Homo sapiens eukaryotic translation initiation factor 1B (EIF1B), mRNA. (from RefSeq NM_005875)

预测能够实现核糖体小亚基结合活性和翻译起始因子活性。预测参与翻译起始过程。预测是真核生物43s起始复合物的一部分。与人类eif1b(真核翻译起始因子1b)有正则关系。[由基因组资源联盟，2022年4月提供]

Orthologous to human EIF1B (eukaryotic translation initiation factor 1B). [provided by Alliance of Genome Resources, Apr 2022] — Master of Bioactive Molecules

Gene Ontology (GO) annotations organized by slimming set. We now provide the "Disease & Variants" viewer in its own tab. The viewer provides 62 variants from UniProt as well as other sources including ClinVar and dbSNP. Go to variant viewer. Showing features for initiator methionine, modified residue, chain, modified residue (large scale data).