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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID 		Cited2
Cbp/p300-interacting transactivator, with Glu/Asp-rich carboxy-terminal domain, 2
MGI:1306784
90 phenotypes from 12 alleles in 15 genetic backgrounds
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Allelic Composition
Genetic Background		 Annotated Term Reference
Cited2m1H/Cited2m1H
involves: BALB/c * C57BL/6J 		no abnormal phenotype detected J:169366
Cited2tm1.1Dunw/Cited2tm1.1Dunw
involves: 129S1/Sv * C57BL/6J 		no abnormal phenotype detected J:117087
Cited2tm1.2Dunw/Cited2tm1.2Dunw
involves: 129S1/Sv * C57BL/6J 		abnormal neural tube morphology J:117087
decreased embryo size J:117087
exencephaly J:117087
hydrops fetalis J:117087
Cited2tm1Bha/Cited2+
involves: 129P2/OlaHsd 		abnormal interventricular septum morphology J:137951
abnormal pulmonary trunk morphology J:137951
double outlet right ventricle J:137951
edema J:137951
postnatal lethality J:137951
Cited2tm1Bha/Cited2tm1Bha
B6.129P2-Cited2tm1Bha 		abnormal aortic arch morphology J:92872
abnormal direction of heart looping J:92872
abnormal embryo turning J:92872
abnormal inferior vena cava morphology J:92872
abnormal tail position or orientation J:92872
common atrioventricular valve J:92872
dextrocardia J:92872
double outlet right ventricle J:92872
interrupted aortic arch J:92872
mesocardia J:92872
persistent truncus arteriosus J:92872
right aortic arch J:92872
right atrial isomerism J:92872
right pulmonary isomerism J:92872
situs inversus J:92872
small spleen J:92872
ventricular septal defect J:92872
Cited2tm1Bha/Cited2tm1Bha
involves: 129 * C57BL/6J 		double outlet right ventricle J:92872
ventricular septal defect J:92872
Cited2tm1Bha/Cited2tm1Bha
involves: 129P2/OlaHsd 		abnormal aortic arch morphology J:102098
abnormal cardiac outflow tract development J:102098
abnormal heart ventricle morphology J:192202
absent adrenal gland J:102098, J:192202
common atrium J:192202
double outlet right ventricle J:102098
ostium primum atrial septal defect J:102098
right aortic arch J:102098
right atrial isomerism J:192202
vascular ring J:102098
ventricular septal defect J:102098, J:192202
Cited2tm1Bha/Cited2tm1Bha
involves: 129P2/OlaHsd * C57BL/6J 		aberrant origin of the right subclavian artery J:76593
abnormal aortic arch morphology J:76593, J:92872
abnormal cardiac neural crest cell morphology J:76593
abnormal cranial ganglia morphology J:76593
abnormal direction of heart looping J:92872
abnormal embryo turning J:92872
abnormal heart atrium morphology J:92872
abnormal heart development J:92872
abnormal heart position or orientation J:92872
abnormal heart ventricle morphology J:92872
abnormal inferior vena cava morphology J:92872
abnormal kidney development J:123322
abnormal tail position or orientation J:92872
absent adrenal gland J:76593
absent cardiac neural crest cells J:76593
atrial septal defect J:76593
common atrioventricular valve J:92872
decreased cardiac neural crest cell number J:76593
double outlet right ventricle J:76593, J:92872
embryonic lethality during organogenesis, incomplete penetrance J:76593, J:123322
exencephaly J:76593
fused dorsal root ganglion J:76593
interrupted aortic arch J:92872
ostium primum atrial septal defect J:92872
overriding aortic valve J:76593
perinatal lethality, complete penetrance J:76593
persistent truncus arteriosus J:76593, J:92872
right aortic arch J:92872
right atrial isomerism J:92872
right pulmonary isomerism J:92872
small dorsal root ganglion J:76593
small spleen J:92872
ventricular septal defect J:76593, J:92872
Cited2tm1Bha/Cited2tm2Bha
Edil3Tg(Sox2-cre)1Amc/Edil3+
involves: 129 * C57BL/6 * CBA * SJL 		abnormal heart left ventricle morphology J:137951
abnormal inferior vena cava morphology J:137951
absent adrenal gland J:137951
absent coronary sinus J:137951
common atrioventricular valve J:137951
dextrocardia J:137951
double outlet right ventricle J:137951
exencephaly J:137951
lethality throughout fetal growth and development, incomplete penetrance J:137951
ostium primum atrial septal defect J:137951
postnatal lethality, complete penetrance J:137951
right aortic arch J:137951
right atrial isomerism J:137951
right pulmonary isomerism J:137951
transposition of great arteries J:137951
ventricular septal defect J:137951
Cited2tm1Bha/Cited2tm2Bha
H2az2Tg(Wnt1-cre)11Rth/H2az2+
involves: 129 * C57BL/6 * CBA * SJL 		abnormal glossopharyngeal ganglion morphology J:137951
abnormal vagus ganglion morphology J:137951
decreased survivor rate J:137951
exencephaly J:137951
postnatal lethality, incomplete penetrance J:137951
small geniculate ganglion J:137951
small trigeminal ganglion J:137951
small vestibular ganglion J:137951
Cited2tm1Bha/Cited2tm2Bha
Mesp1tm2(cre)Ysa/Mesp1+
involves: 129 * C57BL/6 * CBA * SJL 		ventricular septal defect J:137951
Cited2tm1Bha/Cited2tm2Bha
Tg(T-cre)1Lwd/0
involves: 129 * C3H * C57BL/6 * SJL 		abnormal heart left ventricle morphology J:137951
abnormal heart morphology J:137951
absent adrenal gland J:137951
common atrium J:137951
dextrocardia J:137951
double outlet right ventricle J:137951
right atrial isomerism J:137951
right pulmonary isomerism J:137951
ventricular septal defect J:137951
Cited2tm1Bha/Cited2tm3.1Bha
involves: 129P2/OlaHsd * 129S4/SvJaeSor * C57BL/6J 		no abnormal phenotype detected J:192202
Cited2tm1Bha/Cited2tm4Bha
involves: 129P2/OlaHsd * C57BL/6J * C57BL/6N 		no abnormal phenotype detected J:192202
Cited2tm1Bha/Cited2tm5Bha
involves: 129P2/OlaHsd * C57BL/6J * C57BL/6N 		no abnormal phenotype detected J:192202
Cited2tm1Bha/Cited2tm6Bha
involves: 129P2/OlaHsd * C57BL/6J * C57BL/6N 		no abnormal phenotype detected J:192202
Cited2tm1Dunw/Cited2tm1Dunw
involves: 129S1/Sv * C57BL/6J 		no abnormal phenotype detected J:117087
Cited2tm1Jpmb/Cited2tm1Jpmb
involves: 129P2/OlaHsd 		abnormal kidney development J:123322
Cited2tm1Jpmb/Cited2tm1Jpmb
involves: 129P2/OlaHsd * C57BL/6 		abnormal atrioventricular cushion morphology J:97216
abnormal basicranium morphology J:97216
abnormal cranial ganglia morphology J:74736
abnormal direction of heart looping J:97216
abnormal heart morphology J:97216
abnormal left-right axis patterning J:97216
abnormal neural fold formation J:74736
abnormal neurocranium morphology J:74736
abnormal stomach position or orientation J:97216
abnormal truncus arteriosus septation J:74736
decreased atrioventricular cushion size J:97216
decreased fetal size J:74736
edema J:74736
exencephaly J:74736
fused dorsal root ganglion J:74736
normal homeostasis/metabolism phenotype J:74736
increased embryonic neuroepithelium apoptosis J:74736
lethality throughout fetal growth and development, complete penetrance J:74736
open neural tube J:74736
right atrial isomerism J:97216
right pulmonary isomerism J:97216
right-sided isomerism J:97216
ventricular septal defect J:74736
Cited2tm1Ycy/Cited2+
involves: C57BL/6J 		decreased embryo size J:78364
exencephaly J:78364
prenatal lethality, incomplete penetrance J:78364
Cited2tm1Ycy/Cited2tm1Ycy
B6.Cg-Cited2tm1Ycy 		abnormal lung development J:136063
abnormal pulmonary alveolus epithelial cell morphology J:136063
abnormal pulmonary alveolus morphology J:136063
abnormal surfactant secretion J:136063
abnormal type I pneumocyte morphology J:136063
abnormal type II pneumocyte morphology J:136063
absent alveolar lamellar bodies J:136063
impaired lung alveolus development J:136063
right pulmonary isomerism J:136063
small lung lobe J:136063
Cited2tm1Ycy/Cited2tm1Ycy
involves: C57BL/6J 		abnormal blood flow velocity J:78364
abnormal heart and great artery attachment J:78364
abnormal spinal cord central canal morphology J:78364
atrioventricular valve regurgitation J:78364
decreased embryo size J:78364
double outlet right ventricle J:78364
exencephaly J:78364
iris coloboma J:78364
lethality throughout fetal growth and development, complete penetrance J:78364
persistent truncus arteriosus J:78364
pulmonary artery stenosis J:78364
ventricular septal defect J:78364
Cited2tm3.1Bha/Cited2tm3.1Bha
involves: 129S4/SvJaeSor * C57BL/6J 		no abnormal phenotype detected J:192202
Cited2tm5Bha/Cited2tm5Bha
involves: C57BL/6J * C57BL/6N 		no abnormal phenotype detected J:192202
Cited2tm6Bha/Cited2tm6Bha
involves: C57BL/6J * C57BL/6N 		no abnormal phenotype detected J:192202
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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11/19/2024
MGI 6.24 		The Jackson Laboratory