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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID 		Cc2d2a
coiled-coil and C2 domain containing 2A
MGI:1924487
56 phenotypes from 4 alleles in 4 genetic backgrounds
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Allelic Composition
Genetic Background		 Annotated Term Reference
Cc2d2ab2b1035Clo/Cc2d2ab2b1035Clo
C57BL/6J-Cc2d2ab2b1035Clo 		anophthalmia J:175213
atrioventricular septal defect J:175213
biventricular, discordant atrioventricular connection J:175213
cleft palate J:175213
common atrium J:175213
complete atrioventricular septal defect J:175213
double outlet right ventricle J:175213
double outlet right ventricle with atrioventricular septal defect J:175213
duplex kidney J:175213
heterotaxia J:175213
kidney cyst J:175213
microphthalmia J:175213
muscular ventricular septal defect J:175213
persistent truncus arteriosus J:175213
polycystic kidney J:175213
preaxial polydactyly J:175213
prenatal growth retardation J:175213
pulmonary valve atresia J:175213
superior-inferior ventricles J:175213
tricuspid valve atresia J:175213
ventricular septal defect J:175213
Cc2d2aGt(AA0274)Wtsi/Cc2d2aGt(AA0274)Wtsi
involves: 129P2/OlaHsd 		abnormal left-right axis patterning J:176174
abnormal rostral-caudal axis patterning J:176174
normal cellular phenotype J:176174
holoprosencephaly J:176174
microphthalmia J:176174
Cc2d2atm1a(EUCOMM)Wtsi/Cc2d2a+
C57BL/6N-Cc2d2atm1a(EUCOMM)Wtsi/Wtsi 		decreased body weight J:175295
Cc2d2atm1Asw/Cc2d2atm1Asw
Not Specified 		abnormal cochlear hair cell stereociliary bundle morphology J:226310
abnormal embryo development J:226310
abnormal eye electrophysiology J:226310
abnormal kinocilium morphology J:226310
abnormal neural tube morphology J:226310
abnormal nonmotile primary cilium morphology J:226310
abnormal photoreceptor inner segment morphology J:226310
abnormal photoreceptor outer segment morphology J:226310
abnormal primary cilium morphology J:226310
abnormal primitive node morphology J:226310
abnormal renal tubule epithelial cell primary cilium morphology J:226310
abnormal retina morphology J:226310
abnormal retina outer nuclear layer morphology J:226310
abnormal tracheal ciliated epithelium morphology J:226310
abnormal vesicle-mediated transport J:226310
anophthalmia J:226310
decreased embryo size J:226310
decreased embryonic cilium number J:226310
decreased embryonic neuroepithelium primary cilium number J:226310
decreased respiratory motile cilia number J:226310
dextrocardia J:226310
exencephaly J:226310
focal dorsal hair loss J:226310
hemorrhage J:226310
hydrocephaly J:226310
incomplete rostral neuropore closure J:226310
lethality throughout fetal growth and development, incomplete penetrance J:226310
lethargy J:226310
microphthalmia J:226310
polydactyly J:226310
postnatal growth retardation J:226310
preaxial polydactyly J:226310
situs inversus J:226310
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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Send questions and comments to User Support. 		last database update
12/17/2024
MGI 6.24 		The Jackson Laboratory