65 phenotypes from 8 alleles in 11 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Fbn2em1(IMPC)Rbrc/Fbn2em1(IMPC)Rbrc C57BL/6NJcl-Fbn2em1(IMPC)Rbrc/Rbrc	abnormal autopod morphology	J:211773
	abnormal bone structure	J:211773
	abnormal brain morphology	J:211773
	abnormal clavicle morphology	J:211773
	abnormal cranium morphology	J:211773
	abnormal digit morphology	J:211773
	abnormal eye morphology	J:211773
	abnormal femur morphology	J:211773
	abnormal fibula morphology	J:211773
	abnormal gait	J:211773
	abnormal heart morphology	J:211773
	abnormal heart weight	J:211773
	abnormal humerus morphology	J:211773
	abnormal joint morphology	J:211773
	abnormal kidney morphology	J:211773
	abnormal liver morphology	J:211773
	abnormal mandible morphology	J:211773
	abnormal nail morphology	J:211773
	abnormal optic disk morphology	J:211773
	abnormal pelvic girdle bone morphology	J:211773
	abnormal placement of pupils	J:211773
	abnormal radius morphology	J:211773
	abnormal retina blood vessel morphology	J:211773
	abnormal rib morphology	J:211773
	abnormal skin morphology	J:211773
	abnormal tail morphology	J:211773
	abnormal tibia morphology	J:211773
	abnormal ulna morphology	J:211773
	abnormal vertebral arch morphology	J:211773
	abnormal zygomatic bone morphology	J:211773
	corneal opacity	J:211773
	corneal vascularization	J:211773
	decreased anxiety-related response	J:211773
	decreased body length	J:211773
	decreased circulating amylase level	J:211773
	decreased grip strength	J:211773
	enlarged heart	J:211773
	increased bone mineral content	J:211773
	increased circulating alkaline phosphatase level	J:211773
	prolonged ST segment	J:211773
	syndactyly	J:211773
	thrombocytopenia	J:211773
	vertebral fusion	J:211773
Fbn2fp-2J/Fbn2fp-2J involves: C57BL/6J * C.B10-H2b/LiMcdJ	syndactyly	J:68881
Fbn2fp-2J/Fbn2fp-2J involves: C.B10-H2b/LeMcdJ	syndactyly	J:51131
Fbn2fp-3J/Fbn2fp-3J involves: 129S4/SvJae * C57BL/6J	syndactyly	J:60747
Fbn2fp-4J/Fbn2fp-4J BALB/cByJ-Fbn2fp-4J/GrsrJ	fused phalanges	J:211397
	syndactyly	J:211397
	normal vision/eye phenotype	J:211397
Fbn2fp/Fbn2fp C3Fe(B6)-Fbn2fp/J	decreased grip strength	J:157998
	limb grasping	J:157998
	muscle weakness	J:157998
	syndactyly	J:13514, J:157998
Fbn2fp/Fbn2mz involves: BALB/cAnNCrl * C3H/HeH * C3HeB/FeHu * C57BL/6J	decreased grip strength	J:157998
	limb grasping	J:157998
	muscle weakness	J:157998
Fbn2mz/Fbn2mz involves: BALB/cAnNCrl * C3H/HeH	abnormal motor capabilities/coordination/movement	J:157998
	abnormal muscle electrophysiology	J:157998
	centrally nucleated skeletal muscle fibers	J:157998
	decreased body size	J:157998
	decreased grip strength	J:157998
	decreased skeletal muscle fiber diameter	J:157998
	fused phalanges	J:157998
	increased skeletal muscle mass	J:157998
	limb grasping	J:157998
	muscle weakness	J:157998
	postnatal growth retardation	J:157998
	syndactyly	J:157998
Fbn2timon/Fbn2timon C57BL/6J-Fbn2timon	abnormal carpal bone morphology	J:263533
	abnormal ear morphology	J:263533
	abnormal eye morphology	J:263533
	abnormal skeleton morphology	J:263533
	edema	J:263533
	micrognathia	J:263533
	reduced fertility	J:263533
	syndactyly	J:263533
Fbn2tm1Rmz/Fbn2tm1Rmz either: (involves: 129/Sv) or (involves: 129/Sv * C57BL/6J)	abnormal autopod morphology	J:70592
	abnormal interdigital cell death	J:70592
	abnormal joint morphology	J:70592
	normal respiratory system phenotype	J:70592
	syndactyly	J:70592
Fbn2tm1Rmz/Fbn2tm1Rmz involves: 129S/SvEv	abnormal bone remodeling	J:166786
	abnormal skeleton development	J:166786
	decreased bone mass	J:166786