63 phenotypes from 6 alleles in 9 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Fras1b2b3323Clo/Fras1b2b3323Clo C57BL/6J-Fras1b2b3323Clo	abnormal digit morphology	J:175213
	abnormal eye morphology	J:175213
	absent kidney	J:175213
	micrognathia	J:175213
	perimembraneous ventricular septal defect	J:175213
Fras1bfb/Fras1bfb involves: C3H/HeH * C57BL/6JAnu	absent kidney	J:199856
	bleb	J:199856
	cleft secondary palate	J:199856
	eyelids open at birth	J:199856
	preaxial polydactyly	J:199856
Fras1bfb/Fras1bfb involves: C57BL/6JAnu	abnormal palatal shelf fusion at midline	J:208682
	abnormal palatal shelf morphology	J:208682
	abnormal rib morphology	J:208682
	abnormal sternebra morphology	J:208682
	abnormal sternum morphology	J:208682
	absent kidney	J:208682
	bleb	J:208682
	blistering	J:208682
	cleft secondary palate	J:208682
	complete cleft palate	J:208682
	normal craniofacial phenotype	J:208682
	narrow eye opening	J:208682
	preaxial polydactyly	J:208682
	small kidney	J:208682
	subcutaneous hemorrhage	J:208682
Fras1bl/Fras1bl involves: 101/H * C3H/HeH	abnormal basement membrane morphology	J:83745
	abnormal hair growth	J:13501
	abnormal kidney development	J:83745
	abnormal metanephric mesenchyme morphology	J:83745
	abnormal metanephros morphology	J:83745
	abnormal ureteric bud morphology	J:83745
	absent kidney	J:13501, J:83745
	bleb	J:13501
	clubfoot	J:13501, J:83745
	cryptophthalmos	J:83745
	delayed kidney development	J:83745
	fetal bleb	J:83745
	impaired branching involved in ureteric bud morphogenesis	J:83745
	increased metanephric mesenchyme apoptosis	J:83745
	kidney cyst	J:83745
	microphthalmia	J:13501
	prenatal lethality, incomplete penetrance	J:83745
	single kidney	J:13501, J:83745
	small kidney	J:83745
	syndactyly	J:83745
Fras1bl/Fras1tm1.2Pjsc involves: 101/H * C3H/HeH * C57BL/6 * FVB/N * SJL	abnormal glomerular capillary morphology	J:190659
	abnormal glomerular capsule space morphology	J:190659
	abnormal glomerular mesangium morphology	J:190659
	abnormal renal glomerulus morphology	J:190659
	cortical renal glomerulopathies	J:190659
	glomerulosclerosis	J:190659
	normal integument phenotype	J:190659
	normal renal/urinary system phenotype	J:190659
Fras1rdf/Fras1rdf involves: C57BL/6J * FVB/NJ	abnormal digit morphology	J:231083
	abnormal eye morphology	J:231083
	abnormal hindlimb morphology	J:231083
	abnormal interdigital cell death	J:231083
	abnormal limb morphology	J:231083
	abnormal tail tip morphology	J:231083
	absent kidney	J:231083
	blistering	J:231083
	cleft palate	J:231083
	decreased body size	J:231083
	eyelids open at birth	J:231083
	flaky skin	J:231083
	postnatal growth retardation	J:231083
	postnatal lethality, complete penetrance	J:231083
	preaxial polydactyly	J:231083
	short tail	J:231083
	single kidney	J:231083
	syndactyly	J:231083
Fras1tm1.2Pjsc/Fras1tm1.2Pjsc involves: C57BL/6 * FVB/N * SJL	absent kidney	J:190659
	blistering	J:190659
	hemorrhage	J:190659
Fras1tm1Chpk/Fras1tm1Chpk involves: 129S1/Sv * 129X1/SvJ * C57BL/10	absent kidney	J:83746
	blistering	J:83746
	cryptophthalmos	J:83746
	lethality throughout fetal growth and development, complete penetrance	J:83746
	lethality throughout fetal growth and development, incomplete penetrance	J:83746
	syndactyly	J:83746
Fras1tm1Chpk/Fras1tm1Chpk involves: 129S1/Sv * 129X1/SvJ * NMRI	abnormal basement membrane morphology	J:137010
	abnormal lung development	J:137010
	abnormal lung epithelium morphology	J:137010
	abnormal lung morphology	J:137010
	abnormal lung vasculature morphology	J:137010
	fused right lung lobes	J:137010