EIF2B2 (eukaryotic translation initiation factor 2B, subunit 2 beta, 39kDa) is a protein-coding gene. Diseases associated with EIF2B2 include eif2b2-related childhood ataxia with central nervous system hypomyelination/vanishing white matter, and ovarioleukodystrophy, and among its related super-pathways are GTP hydrolysis and joining of the 60S ribosomal subunit and Translation Insulin regulation of translation. GO annotations related to this gene include GTP binding and translation initiation factor activity.
Pathway
Cap-dependent Translation Initiation; Eukaryotic Translation Initiation; Gene Expression; Metabolism of proteins; RNA transport; Recycling of eIF2:GDP;
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