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Frem2my-Ucl
Spontaneous Allele Detail
Nomenclature
Symbol: Frem2my-Ucl
Name: Fras1 related extracellular matrix protein 2; myencephalic blebs, University College of London
MGI ID: MGI:3578641
Synonyms: myUcl
Gene: Frem2  Location: Chr3:53513938-53657355 bp, - strand  Genetic Position: Chr3, 25.24 cM
Mutation
origin
Strain of Origin:  Not Specified
Mutation
description
Allele Type:    Spontaneous
Mutation:    Undefined
 
Mutation detailsThis mutation was identified during the creation of an unrelated transgenic strain. No trace of the transgene sequence could be found.
Inheritance:    Not Specified
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
Disease models
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Expression
In Structures Affected by this Mutation: 1 anatomical structures
Find Mice (IMSR)
Mouse strains and cell lines available from the International Mouse Strain Resource (IMSR)
Carrying this Mutation:  Mouse Strains: 0 strains available      Cell Lines: 0 lines available
Carrying any Frem2 Mutation:  6 strains or lines available
Notes
This allele has a similar phenotype to the my (myelencephalic blebs) mutant.
References
Original:  J:98344 Jadeja S, et al., Identification of a new gene mutated in Fraser syndrome and mouse myelencephalic blebs. Nat Genet. 2005 May;37(5):520-5
All:  2 reference(s)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB), Gene Ontology (GO)
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last database update
09/10/2019
MGI 6.14
The Jackson Laboratory