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Human Disease and Mouse Model Detail
Human Disease Arthrogryposis, Distal, Type 2B; DA2B
OMIM ID: 601680
Synonyms Arthrogryposis Multiplex Congenita, Distal, Type 2B; Arthrogryposis Multiplex Congenita, Distal, Type II, with Craniofacial Abnormalities; Arthrogryposis, Distal; Freeman-Sheldon Syndrome Variant; FSSV; Sheldon-Hall Syndrome; SHS
Genes and
mouse models
Mutations in human and/or mouse homologs are associated with this disease

      *Gene is associated with the disease in this species
      Mouse Homologs Human Homologs Mouse Models Mouse : Human
Homology Class
     Myh3 MYH3*   1:1 Homology
Tnni2 TNNI2*   1:1 Homology
Tnnt3 TNNT3*   1:1 Homology
TPM2*   0:1 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
12/09/2014
MGI 5.20
The Jackson Laboratory