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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Tbx20
T-box 20
MGI:1888496
47 phenotypes from 7 alleles in 7 genetic backgrounds
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Allelic Composition
Genetic Background
Annotated Term Reference
Tbx20em1(IMPC)Mbp/Tbx20+
C57BL/6N-Tbx20em1(IMPC)Mbp/MbpMmucd
abnormal placenta morphology J:211773
increased neutrophil cell number J:211773
Tbx20em1(IMPC)Mbp/Tbx20em1(IMPC)Mbp
C57BL/6N-Tbx20em1(IMPC)Mbp/MbpMmucd
abnormal blood vessel morphology J:211773
abnormal embryo turning J:211773
abnormal forebrain development J:211773
abnormal heart looping J:211773
abnormal heart morphology J:211773
abnormal neural tube closure J:211773
abnormal neural tube morphology J:211773
abnormal optic vesicle formation J:211773
abnormal otic vesicle morphology J:211773
abnormal pharyngeal arch morphology J:211773
abnormal somite shape J:211773
abnormal visceral yolk sac morphology J:211773
abnormal vitelline vasculature morphology J:211773
hemorrhage J:211773
prenatal lethality prior to heart atrial septation J:211773
preweaning lethality, complete penetrance J:211773
Tbx20em1Ona/Tbx20em1Ona
involves: C57BL/6 * DBA
abnormal cardiac outflow tract development J:288309
common ventricle J:288309
Tbx20tm1.1Rph/Tbx20+
involves: C57BL/6
decreased heart left ventricle muscle contractility J:98489
decreased heart left ventricle wall thickness J:98489
dilated cardiomyopathy J:98489
dilated heart left atrium J:98489
dilated heart left ventricle J:98489
Tbx20tm1.1Rph/Tbx20tm1.1Rph
involves: C57BL/6
abnormal body wall morphology J:98489
abnormal fetal cardiomyocyte proliferation J:98489
abnormal heart tube morphology J:98489
abnormal visceral yolk sac mesenchyme morphology J:98489
abnormal vitelline vascular remodeling J:98489
embryonic lethality during organogenesis, complete penetrance J:98489
failure of heart looping J:98489
Tbx20tm1.1Sev/Tbx20tm1.1Sev
involves: 129S6/SvEvTac * C57BL/6
abnormal fetal cardiomyocyte proliferation J:98516
abnormal heart tube morphology J:98516
embryonic growth arrest J:98516
embryonic lethality during organogenesis, complete penetrance J:98516
failure of heart looping J:98516
heart hypoplasia J:98516
Tbx20tm1.2Rph/Tbx20tm1.2Rph
B6.Cg-Tbx20tm1.2Rph
no abnormal phenotype detected J:101977
Tbx20tm1Akis/Tbx20tm1Akis
involves: 129S1/SvImJ * NMRI
abnormal blood circulation J:98806
abnormal fetal cardiomyocyte proliferation J:98806
abnormal heart development J:98806
abnormal heart tube morphology J:98806
abnormal vascular development J:98806
edema J:98806
embryonic growth arrest J:98806
embryonic growth retardation J:98806
embryonic lethality during organogenesis, complete penetrance J:98806
failure of heart looping J:98806
Tbx20tm1Sev/Tbx20tm1.1Sev
Nfatc1tm1.1(cre)Bz/Nfatc1+
involves: 129S1/Sv * 129S6/SvEvTac * 129X1/SvJ * Black Swiss
abnormal cardiovascular system physiology J:198628
abnormal heart valve morphology J:198628
aortic valve regurgitation J:198628
decreased atrioventricular cushion size J:198628
hemorrhage J:198628
lethality throughout fetal growth and development, complete penetrance J:198628
small atrioventricular valve J:198628
small semilunar valve J:198628

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
11/12/2024
MGI 6.24
The Jackson Laboratory