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Phenotype Images associated with this Gene
Symbol
Name
ID
Lama5
laminin, alpha 5
MGI:105382


31 phenotype image(s) for Lama5 alleles
Showing image(s) 11 to 20
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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
Lama5b2b2966.1Clo, 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
Lama5b2b2966.1Clo, 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
Lama5b2b2966.1Clo, 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
Lama5b2b2966.1Clo, 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
Lama5b2b2966.1Clo, 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
Lama5b2b2966.1Clo, 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
Lama5b2b2966.1Clo, 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
Lama5b2b2966.1Clo, 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
Lama5b2b2966.1Clo, 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
Lama5b2b2966.1Clo, 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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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
05/07/2024
MGI 6.23
The Jackson Laboratory