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Symbol
Name
ID
Cfc1
cryptic, EGF-CFC family member 1
MGI:109448
Phenotype annotations related to embryo
Darker colors indicate more annotations
Human Phenotypes
Polyhydramnios
Disease(s) Associated with CFC1
visceral heterotaxy
Disease(s) Associated with CFC1B
visceral heterotaxy

Mouse Phenotypes
abnormal direction of embryo turning
abnormal left-right axis patterning
Availability Mouse Genotype
Cfc1tm1Mms/Cfc1tm1Mms

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
03/19/2024
MGI 6.23
The Jackson Laboratory