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Phenotypes Associated with This Genotype
Genotype
MGI:3579982
Allelic
Composition
Frem2Gt(KST252)Byg/Frem2my-Ucl
Genetic
Background
involves: 129P2/OlaHsd * CD-1 * NMRI
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Frem2Gt(KST252)Byg mutation (1 available); any Frem2 mutation (6 available)
Frem2my-Ucl mutation (0 available); any Frem2 mutation (6 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
integument
• shows epidermal "blebs" during embryogenesis with a frequency and severity indistinguishable from that of mice homozygous for Frem2Ucl

Mouse Models of Human Disease
DO ID OMIM ID(s) Ref(s)
Fraser syndrome DOID:0090001 OMIM:PS219000
J:98344


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
12/03/2019
MGI 6.14
The Jackson Laboratory