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Symbol
Name
ID
Cc2d2a
coiled-coil and C2 domain containing 2A
MGI:1924487
Phenotype annotations related to craniofacial
Darker colors indicate more annotations
Human Phenotypes
Encephalocele
Occipital encephalocele
Cleft upper lip
Cleft palate
Disease(s) Associated with CC2D2A
Joubert syndrome 9
Meckel syndrome 6

Mouse Phenotypes
cleft palate
Availability Mouse Genotype
Cc2d2ab2b1035Clo/Cc2d2ab2b1035Clo

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
04/30/2024
MGI 6.23
The Jackson Laboratory