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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID 		Foxh1
forkhead box H1
MGI:1347465
75 phenotypes from 6 alleles in 4 genetic backgrounds
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Allelic Composition
Genetic Background		 Annotated Term Reference
Foxh1b2b2662Clo/Foxh1b2b2662Clo
C57BL/6J-Foxh1b2b2662Clo 		abdominal situs ambiguus J:175213
abnormal aortic arch morphology J:175213
abnormal cranium morphology J:175213
abnormal inferior vena cava morphology J:175213
abnormal intestine morphology J:175213
abnormal right subclavian artery morphology J:175213
abnormal sternum morphology J:175213
abnormal thoracic cavity morphology J:175213
absent mandible J:175213
absent pericardium J:175213
absent spleen J:175213
acrania J:175213
anencephaly J:175213
anophthalmia J:175213
common atrium J:175213
common ventricle J:175213
cyclopia J:175213
decreased mouth size J:175213
dextrocardia J:175213
diaphragmatic hernia J:175213
double outlet right ventricle with atrioventricular septal defect J:175213
double outlet right ventricle, Taussig bing type J:175213
heart left ventricle hypoplasia J:175213
heterotaxia J:175213
lowered ear position J:175213
mesocardia J:175213
microcephaly J:175213
proboscis J:175213
right aortic arch J:175213
right pulmonary isomerism J:175213
right-sided stomach J:175213
situs inversus with levocardia J:175213
thymus hypoplasia J:175213
vascular ring J:175213
Foxh1tm1Hmd/Foxh1tm1.1Hmd
Tg(Leftb-cre)1Hmd/0
involves: 129S1/Sv * 129X1/SvJ * C57BL/6Cr 		abnormal azygos vein morphology J:82311
abnormal heart position or orientation J:82311
abnormal hepatic portal vein morphology J:82311
abnormal renal vein morphology J:82311
atrial septal defect J:82311
atrial situs inversus J:82311
complete atrioventricular septal defect J:82311
dextrocardia J:82311
double outlet right ventricle J:82311
mesocardia J:82311
postnatal lethality, complete penetrance J:82311
right atrial isomerism J:82311
right pulmonary isomerism J:82311
right-sided isomerism J:82311
right-sided stomach J:82311
spleen hypoplasia J:82311
transposition of great arteries J:82311
ventricular septal defect J:82311
Foxh1tm1Jlw/Foxh1tm1Jlw
involves: 129S1/Sv * 129X1/SvJ * CD-1 		abnormal anterior head development J:69594
abnormal anterior primitive streak morphology J:69594
abnormal cardiac outflow tract development J:93034
abnormal heart development J:93034
abnormal heart left ventricle morphology J:93034
abnormal heart looping J:93034
abnormal heart ventricle morphology J:93034
abnormal mesendoderm development J:69594
abnormal neural plate morphology J:69594
abnormal pericardial cavity morphology J:69594
abnormal pharyngeal arch artery morphology J:93034
absent heart right ventricle J:93034
absent neural folds J:69594
absent notochord J:69594
absent prechordal mesoderm J:69594
absent primitive node J:69594
decreased embryo size J:69594
disorganized myocardium J:93034
embryonic growth retardation J:69594
embryonic lethality during organogenesis, complete penetrance J:69594
embryonic-extraembryonic boundary constriction J:69594
failure of heart looping J:69594
fused somites J:69594
holoprosencephaly J:69594
pericardial edema J:93034
trabecula carnea hypoplasia J:93034
Foxh1tm2.1(Foxh1)Cvw/Foxh1tm2.1(Foxh1)Cvw
involves: 129S6/SvEvTac * C57BL/6 * SJL 		no abnormal phenotype detected J:217681
Foxh1tm3.1(Foxh1*)Cvw/Foxh1tm3.1(Foxh1*)Cvw
involves: 129S6/SvEvTac * C57BL/6 * SJL 		no abnormal phenotype detected J:217681
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
11/12/2024
MGI 6.24 		The Jackson Laboratory