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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...
      Mouse Homologs Human Homologs Mouse Models Mouse : Human
Homology Class
     Eif2b1 EIF2B1*   1:1 Homology
Eif2b2 EIF2B2*   1:1 Homology
Eif2b3 EIF2B3*   1:1 Homology
Eif2b4 EIF2B4*   1:1 Homology
Eif2b5 EIF2B5*   1:1 Homology

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
MGI 5.21
The Jackson Laboratory