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Symbol
Name
ID
Ephb4
Eph receptor B4
MGI:104757
Phenotype annotations related to embryo
Darker colors indicate more annotations
Human Phenotypes
Increased nuchal translucency
Nonimmune hydrops fetalis
Disease(s) Associated with EPHB4
central conducting lymphatic anomaly

Mouse Phenotypes
embryonic growth retardation
abnormal vitelline vascular remodeling
Availability Mouse Genotype
Ephb4tm1And/Ephb4tm1And

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