rs148810263

This variant is located in the EIF2B4 gene.

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ClinVar annotation

Likely Benign★★★☆
6 submitters3 publications

Vanishing white matter disease; not specified; not provided; EIF2B4-related disorder

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About EIF2B4

Eukaryotic initiation factor 2B (EIF2B), which is necessary for protein synthesis, is a GTP exchange factor composed of five different subunits. The protein encoded by this gene is the fourth, or delta, subunit. Defects in this gene are a cause of leukoencephalopathy with vanishing white matter (VWM) and ovarioleukodystrophy. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]

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Gene information from NCBI Gene. Variant classifications from ClinVar.

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