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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Ccdc39
coiled-coil domain containing 39
MGI:1289263
49 phenotypes from 6 alleles in 6 genetic backgrounds
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Allelic Composition
Genetic Background
Annotated Term Reference
Ccdc39b2b1304Clo/Ccdc39b2b1304Clo
C57BL/6J-Ccdc39b2b1304Clo
dextrocardia J:175213
hydronephrosis J:175213
immotile respiratory cilia J:175213
polycystic kidney J:175213
situs inversus totalis J:175213
Ccdc39b2b1735Clo/Ccdc39b2b1735Clo
C57BL/6J-Ccdc39b2b1735Clo
abdominal situs ambiguus J:175213
abdominal situs inversus J:175213
atrial septal defect J:175213
dextrocardia J:175213
double outlet right ventricle J:175213
heterotaxia J:175213
immotile respiratory cilia J:175213
left pulmonary isomerism J:175213
micrognathia J:175213
situs inversus totalis J:175213
vascular ring J:175213
Ccdc39b2b2025.1Clo/Ccdc39b2b2025.1Clo
C57BL/6J-Ccdc39b2b2025.1Clo
abnormal aortic arch morphology J:175213
abnormal inferior vena cava morphology J:175213
abnormal liver morphology J:175213
absent spleen J:175213
atrioventricular septal defect J:175213
dextrocardia J:175213
double outlet right ventricle J:175213
double outlet right ventricle with atrioventricular septal defect J:175213
double outlet right ventricle, Taussig bing type J:175213
dual inferior vena cava J:175213
heterotaxia J:175213
interrupted aortic arch J:175213
l-loop transposition of the great arteries J:175213
left atrial isomerism J:175213
left pulmonary isomerism J:175213
muscular ventricular septal defect J:175213
overriding aortic valve J:175213
perimembraneous ventricular septal defect J:175213
right atrial isomerism J:175213
right-sided stomach J:175213
spleen hypoplasia J:175213
superior-inferior ventricles J:175213
vascular ring J:175213
Ccdc39prh/Ccdc39prh
involves: A/J * FVB/N
abnormal brain development J:253968
abnormal brain ependyma motile cilium morphology J:253968
abnormal brain ependyma motile cilium physiology J:253968
abnormal cerebrospinal fluid flow J:253968
abnormal cortical ventricular zone morphology J:253968
abnormal postnatal subventricular zone morphology J:253968
decreased body weight J:253968
dilated lateral ventricle J:174027
dilated third ventricle J:174027
dysmyelination J:253968
enlarged brain ventricles J:253968
gliosis J:253968
heterotaxia J:253968
hydrocephaly J:174027, J:253968
postnatal lethality, complete penetrance J:253968
right-sided stomach J:253968
situs inversus totalis J:253968
small olfactory bulb J:253968
Ccdc39prh/Ccdc39tm1a(KOMP)Wtsi
involves: A/J * C57BL/6N * FVB/N
decreased body weight J:253968
enlarged brain ventricles J:253968
enlarged lateral ventricles J:253968
hydrocephaly J:253968
postnatal lethality, complete penetrance J:253968
Ccdc39tm2b(KOMP)Wtsi/Ccdc39tm2b(KOMP)Wtsi
C57BL/6N-Ccdc39tm2b(KOMP)Wtsi/Tcp
preweaning lethality, complete penetrance J:211773
preweaning lethality, incomplete penetrance J:211773

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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
11/12/2024
MGI 6.24
The Jackson Laboratory