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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Mrtfb
myocardin related transcription factor B
MGI:3050795
42 phenotypes from 5 alleles in 7 genetic backgrounds
Export: Excel File
Allelic Composition
Genetic Background
Annotated Term Reference
Mrtfbem1Dsr/Mrtfbem1Dsr
involves: C57BL/6J
abnormal heart ventricle morphology J:277399
MrtfbGt(RRJ478)Byg/MrtfbGt(RRJ478)Byg
involves: 129P2/OlaHsd
abnormal pharyngeal arch artery morphology J:160964
absent aorticopulmonary septum J:160964
congestive heart failure J:160964
double outlet right ventricle J:160964
edema J:160964
impaired cardiac neural crest cell differentiation J:160964
interrupted aortic arch J:160964
perinatal lethality, incomplete penetrance J:160964
persistent truncus arteriosus J:160964
right aortic arch J:160964
ventricular septal defect J:160964
MrtfbGt(RRJ478)Byg/MrtfbGt(RRJ478)Byg
involves: 129P2/OlaHsd * C57BL/6J
abnormal heart morphology J:117226
abnormal liver morphology J:117226
abnormal visceral yolk sac morphology J:117226
abnormal vitelline vein morphology J:117226
lethality throughout fetal growth and development, incomplete penetrance J:117226
liver hemorrhage J:117226
pale yolk sac J:117226
persistent truncus arteriosus J:117226
thin myocardium J:117226
ventricular septal defect J:117226
MrtfbGt(RRJ478)Byg/MrtfbGt(RRJ478)Byg
H2az2Tg(Wnt1-cre)11Rth/H2az2+
involves: 129P2/OlaHsd * C57BL/6J * CBA/J
lethality throughout fetal growth and development, incomplete penetrance J:117226
Mrtfbtm1.1Msp/Mrtfbtm1.1Msp
involves: 129
abnormal aorta tunica media morphology J:187713
abnormal artery morphology J:187713
abnormal cardiac outflow tract development J:187713
abnormal cell adhesion J:187713
abnormal common carotid artery morphology J:187713
abnormal descending thoracic aorta morphology J:187713
aneurysm J:187713
aortic aneurysm J:187713
dilated aorta J:187713
dilated basilar artery J:187713
dilated third pharyngeal arch artery J:187713
internal hemorrhage J:187713
lethality throughout fetal growth and development, complete penetrance J:187713
liver hemorrhage J:187713
lung hemorrhage J:187713
Mrtfbtm1Eno/Mrtfbtm1Eno
involves: 129S/SvEv * C57BL/6
abnormal fourth pharyngeal arch artery morphology J:102475
abnormal heart and great vessel attachment J:102475
abnormal pharyngeal arch artery morphology J:102475
abnormal sixth pharyngeal arch artery morphology J:102475
double outlet right ventricle J:102475
hemorrhage J:102475
lethality throughout fetal growth and development, complete penetrance J:102475
pericardial edema J:102475
perimembraneous ventricular septal defect J:102475
thin myocardium J:102475
vascular smooth muscle hypoplasia J:102475
Mrtfbtm2.1Eno/Mrtfbtm2.1Eno
Tg(GFAP-cre)25Mes/0
involves: 129S/SvEv * C57BL/6 * FVB/N
no abnormal phenotype detected J:161853

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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
04/30/2024
MGI 6.23
The Jackson Laboratory