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Symbol
Name
ID
Rnf2
ring finger protein 2
MGI:1101759
Phenotype annotations related to embryo
Darker colors indicate more annotations
Human Phenotypes
Oligohydramnios
Disease(s) Associated with RNF2
Luo-Schoch-Yamamoto syndrome

Mouse Phenotypes
abnormal mesoderm development
failure to gastrulate
embryonic growth arrest
abnormal embryonic epiblast morphology
Availability Mouse Genotype
Rnf2tm1Mvl/Rnf2tm1Mvl

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
04/16/2024
MGI 6.23
The Jackson Laboratory