Phenotypes for Frem2 MGI:3579982 MGI Mouse

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Phenotypes Associated with This Genotype

Allelic Composition	Frem2^{Gt(KST252)Byg}/Frem2^my-Ucl
Genetic Background	involves: 129P2/OlaHsd * CD-1 * NMRI

Find Mice

Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Frem2^{Gt(KST252)Byg} mutation (2 available); any Frem2 mutation (137 available)
Frem2^my-Ucl mutation (0 available); any Frem2 mutation (137 available)

♀	phenotype observed in females
♂	phenotype observed in males
N	normal phenotype

integument

bleb ( J:98344 )

• shows epidermal "blebs" during embryogenesis with a frequency and severity indistinguishable from that of mice homozygous for Frem2^Ucl

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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