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Human Disease and Mouse Model Detail
Human Disease Ullrich Congenital Muscular Dystrophy 1; UCMD1
OMIM ID: 254090
Synonyms Muscular Dystrophy, Scleroatonic; Ullrich Congenital Muscular Dystrophy; Ullrich Congenital Muscular Dystrophy; UCMD; Ullrich Disease; Ullrich Scleroatonic Muscular Dystrophy
View all models View ALL (1) mouse models for this human disease.
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
     COL6A3* Col6a3* View 1 model HomoloGene and HGNC
     COL6A1* Col6a1   HomoloGene
COL6A2* Col6a2   HomoloGene
References Disease References using Mouse Models (1)

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 6.03
The Jackson Laboratory