About   Help   FAQ
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
Export: Excel File
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)
Citing These Resources
Funding Information
Warranty Disclaimer, Privacy Notice, Licensing, & Copyright
Send questions and comments to User Support. 		last database update
12/10/2024
MGI 6.24 		The Jackson Laboratory