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GENE - TERM ANNOTATION REPORT

RGD ID: 18912396
Species: Heterocephalus glaber
RGD Object: Gene
Symbol: Eif2b2
Name: eukaryotic translation initiation factor 2B subunit beta
Acc ID: DOID:0070373
Term: leukoencephalopathy with vanishing white matter 2
Definition: A leukoencephalopathy with vanishing white matter that has_material_basis_in homozygous or compound heterozygous mutation in the EIF2B2 gene on chromosome 14q24. (DO)
Definition Source(s): https://pubmed.ncbi.nlm.nih.gov/34745209/ "DO" "DO", https://www.omim.org/entry/620312 "DO" "DO"
Note: Use of the qualifier "multiple interactions" designates that the annotated interaction is comprised of a complex set of reactions and/or regulatory events, possibly involving additional chemicals and/or gene products.
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