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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) 21 to 24 		Show   figures per page Start Previous
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Caption: Mutant (E14.5) shows heterotaxy with dextrocardia and anterior placement of the aorta, suggesting outflow tract malalignment defects. (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) presents with severe craniofacial defects including anencephaly, agnathia, anopthalmia, low-set ears, acrania, phenotypes consistent with otocephaly. (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 (ED14.5) in the coronal plane reveals heterotaxy, dextrocardia, Taussig Bing type double outlet right ventricle (DORV), unbalanced atrioventricular septal defect, common atrium, IVC connected at the middle of the atrium {A,L,L}, TAPVR (to right SVC), aberrant right aortic arch and pulmonary arch anomalies forming incomplete vascular ring, aberrant semilunar valve formation (cushion like), 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
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
11/19/2024
MGI 6.24 		The Jackson Laboratory