Phenotype Images associated with this Gene

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Phenotype Images associated with this Gene

Symbol
Name
ID

b2b2966Clo
Mutant line 2966 Cecilia Lo
MGI:5646288

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	Caption: Color flow spectral Doppler imaging of mutant 2966-005-1 (E15.5) in the sagittal view shows only Ao riding over the interventricular septum with regurgitation, suggesting overriding Ao with possible PA stenosis Click thumbnail to play movie. (details) Represented Alleles: b2b2966Clo, Mutant line 2966 Cecilia Lo; Bench to Bassinet Program (B2B/CVDC), mutation 2966 Cecilia Lo Lama5^b2b2966.1Clo, laminin, alpha 5; Bench to Bassinet Program (B2B/CVDC), mutation 2966, subline 1 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 2966-005-1 (E15.5) presents with exencephaly, low-set ears, and microphthalmia. (details) Represented Alleles: b2b2966Clo, Mutant line 2966 Cecilia Lo; Bench to Bassinet Program (B2B/CVDC), mutation 2966 Cecilia Lo Lama5^b2b2966.1Clo, laminin, alpha 5; Bench to Bassinet Program (B2B/CVDC), mutation 2966, subline 1 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 2966-005-1 (E15.5) shows exencephaly with narrow snout and microphthalmia. (details) Represented Alleles: b2b2966Clo, Mutant line 2966 Cecilia Lo; Bench to Bassinet Program (B2B/CVDC), mutation 2966 Cecilia Lo Lama5^b2b2966.1Clo, laminin, alpha 5; Bench to Bassinet Program (B2B/CVDC), mutation 2966, subline 1 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 2966-005-1 (E15.5) exhibits syndactyly and a curly tail. (details) Represented Alleles: b2b2966Clo, Mutant line 2966 Cecilia Lo; Bench to Bassinet Program (B2B/CVDC), mutation 2966 Cecilia Lo Lama5^b2b2966.1Clo, laminin, alpha 5; Bench to Bassinet Program (B2B/CVDC), mutation 2966, subline 1 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 2966-005-1 (E15.5) presents with absent right thymus gland and a hypoplastic left thymus gland. (details) Represented Alleles: b2b2966Clo, Mutant line 2966 Cecilia Lo; Bench to Bassinet Program (B2B/CVDC), mutation 2966 Cecilia Lo Lama5^b2b2966.1Clo, laminin, alpha 5; Bench to Bassinet Program (B2B/CVDC), mutation 2966, subline 1 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 2966-005-1 (E15.5) presents with abnormal possibly cystic right kidney and hypoplastic left kidney (details) Represented Alleles: b2b2966Clo, Mutant line 2966 Cecilia Lo; Bench to Bassinet Program (B2B/CVDC), mutation 2966 Cecilia Lo Lama5^b2b2966.1Clo, laminin, alpha 5; Bench to Bassinet Program (B2B/CVDC), mutation 2966, subline 1 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 2966-004-NA shows a right aortic arch and fused outflow tracts which is diagnosed as persistent truncus arteriosis (PTA) (Type-I) with interrupted aortic arch (type B) by episcopic confocal microscopy histopathology (details) Represented Alleles: b2b2966Clo, Mutant line 2966 Cecilia Lo; Bench to Bassinet Program (B2B/CVDC), mutation 2966 Cecilia Lo Lama5^b2b2966.1Clo, laminin, alpha 5; Bench to Bassinet Program (B2B/CVDC), mutation 2966, subline 1 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: 2966-004-NA mutant exhibits persistent truncus arteriosus (type 1), atrioventricular septal disorder, right aortic arch, interrupted aortic arch (type B), and abnormal 4th arch development as seen by episcopic confocal microscopy. (details) Represented Alleles: b2b2966Clo, Mutant line 2966 Cecilia Lo; Bench to Bassinet Program (B2B/CVDC), mutation 2966 Cecilia Lo Lama5^b2b2966.1Clo, laminin, alpha 5; Bench to Bassinet Program (B2B/CVDC), mutation 2966, subline 1 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 episcopic confocal microscopy image stack of 2966-004-NA in the coronal plane reveals persistent truncus arteriosis (PTA, Type-I), atrioventricular septal defect (AVSD), right aortic arch (RAA), interrupted aortic arch (IAA, type B) and abnormal 4th arch development. Click thumbnail to play movie. (details) Represented Alleles: b2b2966Clo, Mutant line 2966 Cecilia Lo; Bench to Bassinet Program (B2B/CVDC), mutation 2966 Cecilia Lo Lama5^b2b2966.1Clo, laminin, alpha 5; Bench to Bassinet Program (B2B/CVDC), mutation 2966, subline 1 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 2966-004-NA exhibits a short snout, micrognathia, low set ears, microphthalmia of the right eye, microstomia, and syndactyly on all limbs. (details) Represented Alleles: b2b2966Clo, Mutant line 2966 Cecilia Lo; Bench to Bassinet Program (B2B/CVDC), mutation 2966 Cecilia Lo Lama5^b2b2966.1Clo, laminin, alpha 5; Bench to Bassinet Program (B2B/CVDC), mutation 2966, subline 1 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

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