Phenotype Images associated with this Allele - MGI

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Phenotype Images associated with this Allele

Nomenclature

Symbol:	Fuz^b2b1273Clo
Name:	fuzzy planar cell polarity protein; Bench to Bassinet Program (B2B/CVDC), mutation 1273 Cecilia Lo
MGI ID:	MGI:5311392
Synonyms:	octomouse

Images for
Allele

Click images for details

Image	Caption	Genotypes involving this allele
Image	Caption	Allelic Composition	Genetic Background
	Pulmonary atresia, dual IVC and single left lung lobe seen in mutant 1273-002-1 (E16.5)	Fuz^b2b1273Clo/Fuz^b2b1273Clo	C57BL/6J-Fuz^b2b1273Clo
	EFIC Summary	Fuz^b2b1273Clo/Fuz^b2b1273Clo	C57BL/6J-Fuz^b2b1273Clo
	2D serial EFIC image stack in the coronal view of mutant 1273-002-1 (E16.5) reveals pulmonary atresia, AVSD, right aortic arch, vascular sling, and hypoplastic lung Click thumbnail to play movie.	Fuz^b2b1273Clo/Fuz^b2b1273Clo	C57BL/6J-Fuz^b2b1273Clo
	2D serial EFIC image stack in the transverse view of mutant 1273-002-1 (E16.5) reveals pulmonary atresia, AVSD, right aortic arch, vascular sling, hypoplastic lung, and TEF Click thumbnail to play movie.	Fuz^b2b1273Clo/Fuz^b2b1273Clo	C57BL/6J-Fuz^b2b1273Clo
	Pulmonary atresia, single left lung lobe, right aortic arch and diaphragmatic hernia with liver protruding into chest cavity in mutant 1273-002-2 (E16.5)	Fuz^b2b1273Clo/Fuz^b2b1273Clo	C57BL/6J-Fuz^b2b1273Clo
	EFIC Summary	Fuz^b2b1273Clo/Fuz^b2b1273Clo	C57BL/6J-Fuz^b2b1273Clo
	2D serial EFIC image stack in the coronal view of mutant 1273-002-2 (E16.5) reveals pulmonary atresia, AVSD, right aortic arch, vascular sling, and hypoplastic lung Click thumbnail to play movie.	Fuz^b2b1273Clo/Fuz^b2b1273Clo	C57BL/6J-Fuz^b2b1273Clo
	2D serial EFIC image stack in the transverse view of mutant 1273-002-2 (E16.5) reveals pulmonary atresia, AVSD, right aortic arch, vascular sling, hypoplastic lung, and TEF Click thumbnail to play movie.	Fuz^b2b1273Clo/Fuz^b2b1273Clo	C57BL/6J-Fuz^b2b1273Clo
	Mutants 1273-002-1 and 2 (E16.5) show micrognathia and anophthalmia with severe hydrops	Fuz^b2b1273Clo/Fuz^b2b1273Clo	C57BL/6J-Fuz^b2b1273Clo
	Mutant 1273-002-2 (E16.5) show anophthalmia and craniofacial dysmorphism	Fuz^b2b1273Clo/Fuz^b2b1273Clo	C57BL/6J-Fuz^b2b1273Clo
	Mutant 1273-002-2 (E16.5) shows craniofacial dysmorphism with anophthalmia	Fuz^b2b1273Clo/Fuz^b2b1273Clo	C57BL/6J-Fuz^b2b1273Clo
	Mutant 1273-002-2 (E16.5) shows forelimb central polydactyly with 9 digits	Fuz^b2b1273Clo/Fuz^b2b1273Clo	C57BL/6J-Fuz^b2b1273Clo
	Mutant 1273-002-2 (E16.5) shows hindlimb polydactyly with preaxial digit duplication	Fuz^b2b1273Clo/Fuz^b2b1273Clo	C57BL/6J-Fuz^b2b1273Clo
	Mutant 1273-002-2 (E16.5) shows hindlimb polydactyly with preaxial digit duplication	Fuz^b2b1273Clo/Fuz^b2b1273Clo	C57BL/6J-Fuz^b2b1273Clo
	Mutant 1273-002-2 (E16.5) exhibit a shortened gut	Fuz^b2b1273Clo/Fuz^b2b1273Clo	C57BL/6J-Fuz^b2b1273Clo
	Mutant 1273-002-2 (E16.5) show renal dysplasia	Fuz^b2b1273Clo/Fuz^b2b1273Clo	C57BL/6J-Fuz^b2b1273Clo

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