About   Help   FAQ
Human Disease and Mouse Model Detail
Human Disease Leukoencephalopathy with Vanishing White Matter; VWM
OMIM ID: 603896
Synonyms Childhood Ataxia with Central Nervous System Hypomyelinization; CACH; Vanishing White Matter Leukodystrophy
Genes and
mouse models
Mutations in human and/or mouse homologs are associated with this disease

      *Disease is associated/modeled with this Gene or a homolog. More...
      Human Homologs Mouse Homologs Mouse Models Homology Source
     EIF2B1* Eif2b1   HomoloGene
EIF2B2* Eif2b2   HomoloGene and HGNC
EIF2B3* Eif2b3   HomoloGene and HGNC
EIF2B4* Eif2b4   HomoloGene
EIF2B5* Eif2b5   HomoloGene and HGNC

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
Citing These Resources
Funding Information
Warranty Disclaimer & Copyright Notice
Send questions and comments to User Support.
last database update
07/21/2015
MGI 5.22
The Jackson Laboratory