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Phenotype Images associated with this Gene
Symbol
Name
ID
Foxh1
forkhead box H1
MGI:1347465


24 phenotype image(s) for Foxh1 alleles
Showing image(s) 11 to 20
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Click on allele symbol for full phenotype details.

Caption: Serial 2D ECM image stack of mutant in the coronal plane reveals mesocardia {A,L,L}, Taussig Bing double outlet right ventricle, unbalanced atrioventricular septal defect, common atrium, hypoplastic LV, RAA, right inferior vena cava and left hepatic vein connecting to atrium, and right lung isomerism
Click thumbnail to play movie. (details)
Represented Alleles:
Foxh1b2b2662Clo, forkhead box H1; Bench to Bassinet Program (B2B/CVDC), mutation 2662 Cecilia Lo
Copyright: This image is from the Laboratory of Dr. Cecilia Lo, a member of the Cardiovascular Development Consortium (CvDC), Bench to Bassinet (B2B) program of the National Heart Lung and Blood Institute (NHLBI), and is displayed with the permission of the authors. J:175213
Caption: Serial 2D ECM image stack of mutant in the coronal plane of whole body reveals right diaphragmatic hernia. mesocardia, (A,L,L), Taussig Bing DORV, unbalanced AVSD, common atrium, hypoplatic LV, RAA, right IVC and left hepatic vein connect to atrium, right lung isomerism.
Click thumbnail to play movie.(details)
Represented Alleles:
Foxh1b2b2662Clo, forkhead box H1; Bench to Bassinet Program (B2B/CVDC), mutation 2662 Cecilia Lo
Copyright: This image is from the Laboratory of Dr. Cecilia Lo, a member of the Cardiovascular Development Consortium (CvDC), Bench to Bassinet (B2B) program of the National Heart Lung and Blood Institute (NHLBI), and is displayed with the permission of the authors. J:175213
Caption: Mutant presents with malaligned sternum. (details)
Represented Alleles:
Foxh1b2b2662Clo, forkhead box H1; Bench to Bassinet Program (B2B/CVDC), mutation 2662 Cecilia Lo
Copyright: This image is from the Laboratory of Dr. Cecilia Lo, a member of the Cardiovascular Development Consortium (CvDC), Bench to Bassinet (B2B) program of the National Heart Lung and Blood Institute (NHLBI), and is displayed with the permission of the authors. J:175213
Caption: Mutant shows severe craniofacial defects with anencephaly, acrania, agnathia, and anopthalmia. (details)
Represented Alleles:
Foxh1b2b2662Clo, forkhead box H1; Bench to Bassinet Program (B2B/CVDC), mutation 2662 Cecilia Lo
Copyright: This image is from the Laboratory of Dr. Cecilia Lo, a member of the Cardiovascular Development Consortium (CvDC), Bench to Bassinet (B2B) program of the National Heart Lung and Blood Institute (NHLBI), and is displayed with the permission of the authors. J:175213
Caption: Mutant exhibits microstomia with skin tags that may be abnormally positioned pinnae. (details)
Represented Alleles:
Foxh1b2b2662Clo, forkhead box H1; Bench to Bassinet Program (B2B/CVDC), mutation 2662 Cecilia Lo
Copyright: This image is from the Laboratory of Dr. Cecilia Lo, a member of the Cardiovascular Development Consortium (CvDC), Bench to Bassinet (B2B) program of the National Heart Lung and Blood Institute (NHLBI), and is displayed with the permission of the authors. J:175213
Caption: Mutant exhibits right diaphragmatic hernia with stomach in the thoracic cavity, and also seen is intestinal malrotation. (details)
Represented Alleles:
Foxh1b2b2662Clo, forkhead box H1; Bench to Bassinet Program (B2B/CVDC), mutation 2662 Cecilia Lo
Copyright: This image is from the Laboratory of Dr. Cecilia Lo, a member of the Cardiovascular Development Consortium (CvDC), Bench to Bassinet (B2B) program of the National Heart Lung and Blood Institute (NHLBI), and is displayed with the permission of the authors. J:175213
Caption: EFIC Summary (details)
Represented Alleles:
Foxh1b2b2662Clo, forkhead box H1; Bench to Bassinet Program (B2B/CVDC), mutation 2662 Cecilia Lo
Copyright: This image is from the Laboratory of Dr. Cecilia Lo, a member of the Cardiovascular Development Consortium (CvDC), Bench to Bassinet (B2B) program of the National Heart Lung and Blood Institute (NHLBI), and is displayed with the permission of the authors. J:175213
Caption: Serial 2D ECM image stack of mutant in the coronal plane reveals Taussig-Bing type DORV {A,D,D}, RAA, unbalanced AVSD, common atrium, hypoplastic LV, and right lung isomerism
Click thumbnail to play movie. (details)
Represented Alleles:
Foxh1b2b2662Clo, forkhead box H1; Bench to Bassinet Program (B2B/CVDC), mutation 2662 Cecilia Lo
Copyright: This image is from the Laboratory of Dr. Cecilia Lo, a member of the Cardiovascular Development Consortium (CvDC), Bench to Bassinet (B2B) program of the National Heart Lung and Blood Institute (NHLBI), and is displayed with the permission of the authors. J:175213
Caption: Serial micro-MRI image stack of mutant in the coronal plane reveals double outlet right ventricle (DORV), unbalanced atrioventricular septal defect (AVSD), hypoplastic LV. Bilateral anophthamial, craniofacial hypoplasia, microcephaly, micrognathia or agnathia.
Click thumbnail to play movie. (details)
Represented Alleles:
Foxh1b2b2662Clo, forkhead box H1; Bench to Bassinet Program (B2B/CVDC), mutation 2662 Cecilia Lo
Copyright: This image is from the Laboratory of Dr. Cecilia Lo, a member of the Cardiovascular Development Consortium (CvDC), Bench to Bassinet (B2B) program of the National Heart Lung and Blood Institute (NHLBI), and is displayed with the permission of the authors. J:175213
Caption: Mutant (E14.5) exhibits heterotaxy with dextrocardia. (details)
Represented Alleles:
Foxh1b2b2662Clo, forkhead box H1; Bench to Bassinet Program (B2B/CVDC), mutation 2662 Cecilia Lo
Copyright: This image is from the Laboratory of Dr. Cecilia Lo, a member of the Cardiovascular Development Consortium (CvDC), Bench to Bassinet (B2B) program of the National Heart Lung and Blood Institute (NHLBI), and is displayed with the permission of the authors. J:175213

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
04/23/2024
MGI 6.23
The Jackson Laboratory