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Human Disease and Mouse Model Detail
Human Disease Vasculopathy, Retinal, with Cerebral Leukodystrophy; RVCL
OMIM ID: 192315
Human Phenotype Ontology associations
Synonyms Cerebroretinal Vasculopathy, Hereditary; CRV; Retinopathy, Vascular, with Cerebral and Renal Involvement and Raynaud and Migraine Phenomena
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
     TREX1* Trex1   HomoloGene and HGNC

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 6.07
The Jackson Laboratory