130 phenotypes from 7 alleles in 6 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Hspg2tm1.1Rdgr/Hspg2tm1.1Rdgr involves: 129S1/Sv * 129X1/SvJ	abnormal long bone epiphyseal plate proliferative zone	J:121855
	abnormal long bone hypertrophic chondrocyte zone	J:121855
	normal skeleton phenotype	J:121855
Hspg2tm1.1Soni/Hspg2tm1.1Soni involves: 129S/SvEv * C57BL/6	abnormal behavior	J:139975
	abnormal endplate potential	J:139975
	abnormal joint morphology	J:139975
	abnormal miniature endplate potential	J:139975
	abnormal muscle electrophysiology	J:139975
	abnormal neuromuscular synapse morphology	J:139975
	abnormal skeletal muscle fiber morphology	J:139975
	abnormal skeletal muscle fiber type ratio	J:139975
	centrally nucleated skeletal muscle fibers	J:139975
	chondrodystrophy	J:139975
	decreased body length	J:139975
	decreased body weight	J:139975
	delayed eyelid opening	J:139975
	increased variability of skeletal muscle fiber size	J:139975
	premature death	J:139975
Hspg2tm1Nid/Hspg2tm1Nid involves: 129X1/SvJ * C57BL/6	abnormal bone ossification	J:67299
	abnormal cartilage development	J:67299
	abnormal cartilage morphology	J:67299
	abnormal craniofacial morphology	J:67299
	abnormal cranium morphology	J:67299
	abnormal forelimb morphology	J:67299
	abnormal hindlimb morphology	J:67299
	abnormal long bone hypertrophic chondrocyte zone	J:67299
	abnormal neuromuscular synapse morphology	J:74542
	abnormal skeleton morphology	J:67299
	abnormal vertebral body morphology	J:67299
	decreased chondrocyte proliferation	J:67299
	delayed bone ossification	J:67299
	disorganized long bone epiphyseal plate	J:67299
	disproportionate dwarf	J:67299
	domed cranium	J:67299
	embryonic lethality during organogenesis, incomplete penetrance	J:67299
	exencephaly	J:67299
	perinatal lethality, incomplete penetrance	J:67299
	respiratory failure	J:67299
	short limbs	J:67299
	short mandible	J:67299
	short snout	J:67299
	wide cranial sutures	J:67299
Hspg2tm1Rdgr/Hspg2tm1Rdgr involves: 129S1/Sv * 129X1/SvJ	abnormal bone marrow morphology	J:121855
	abnormal bone ossification	J:121855
	abnormal bone structure	J:121855
	abnormal cell physiology	J:121855
	abnormal femur head morphology	J:121855
	abnormal femur neck morphology	J:121855
	abnormal gait	J:121855
	abnormal humerus morphology	J:121855
	abnormal locomotor coordination	J:121855
	abnormal long bone epiphyseal plate morphology	J:121855
	abnormal long bone epiphysis morphology	J:121855
	abnormal long bone morphology	J:121855
	abnormal muscle morphology	J:121855
	abnormal osteoclast morphology	J:121855
	abnormal pelvic girdle bone morphology	J:121855
	abnormal skeleton morphology	J:121855
	abnormal sternum morphology	J:121855
	abnormal trabecular bone morphology	J:121855
	abnormal vertebral column morphology	J:121855
	bowed humerus	J:121855
	decreased body length	J:121855
	decreased body weight	J:121855
	decreased cranium height	J:121855
	decreased length of long bones	J:121855
	delayed bone ossification	J:121855
	flat face	J:121855
	increased diameter of humerus	J:121855
	increased diameter of long bones	J:121855
	increased osteoclast cell number	J:121855
	increased width of hypertrophic chondrocyte zone	J:121855
	microphthalmia	J:121855
	osteoarthritis	J:121855
	short femur	J:121855
	short femur neck	J:121855
	skeletal muscle hyperplasia	J:121855
Hspg2tm1Ref/Hspg2tm1Ref involves: 129S1/Sv * 129X1/SvJ	abnormal aortic valve morphology	J:80720
	abnormal ascending aorta and coronary artery attachment	J:107987
	abnormal bone marrow cavity morphology	J:58700
	abnormal brain morphology	J:58700
	abnormal cardiac outflow tract development	J:80720
	abnormal cardinal vein morphology	J:80720
	abnormal cartilage development	J:84739
	abnormal cartilage morphology	J:58700
	abnormal chest morphology	J:84739
	abnormal chondrocyte morphology	J:58700
	abnormal conotruncus septation	J:80720
	abnormal cranium morphology	J:58700
	abnormal endochondral bone ossification	J:84739
	abnormal ethmoid bone morphology	J:58700
	abnormal heart and great artery attachment	J:107987
	abnormal inner ear morphology	J:58700
	abnormal intervertebral disk development	J:84739
	abnormal long bone epiphyseal plate morphology	J:58700, J:84739
	abnormal long bone hypertrophic chondrocyte zone	J:58700, J:84739
	abnormal long bone metaphysis morphology	J:84739
	abnormal long bone morphology	J:58700, J:84739
	abnormal middle ear morphology	J:58700
	abnormal myocardium compact layer morphology	J:58700
	abnormal myocardium layer morphology	J:80720
	abnormal nervous system morphology	J:58700
	abnormal occipital bone morphology	J:58700
	abnormal pericardium morphology	J:58700
	abnormal pulmonary valve morphology	J:80720
	abnormal rib morphology	J:84739
	abnormal semilunar valve morphology	J:80720
	abnormal skeleton morphology	J:58700
	abnormal sphenoid bone morphology	J:58700
	abnormal spine curvature	J:58700
	abnormal telencephalon morphology	J:58700
	absent conotruncal ridges	J:80720
	absent frontal bone	J:58700
	absent neurocranium	J:58700
	absent parietal bone	J:58700
	aneurysm	J:58700
	chondrodystrophy	J:58700, J:84739
	cleft palate	J:58700
	conotruncal ridge hyperplasia	J:80720
	decreased body length	J:84739
	decreased bone mineralization	J:58700
	decreased embryo size	J:84739
	decreased length of long bones	J:58700
	dilated liver sinusoidal space	J:80720
	disorganized long bone epiphyseal plate	J:58700
	disproportionate dwarf	J:58700, J:84739
	domed cranium	J:58700
	embryonic lethality during organogenesis, incomplete penetrance	J:58700
	enlarged vertebral body	J:84739
	exencephaly	J:58700
	hemopericardium	J:58700
	hemorrhage	J:58700
	impaired basement membrane formation	J:58700
	increased compact bone thickness	J:58700
	intracranial hemorrhage	J:58700
	irregular heartbeat	J:58700
	lung hemorrhage	J:58700
	perinatal lethality, incomplete penetrance	J:58700
	short limbs	J:58700
	short mandible	J:58700
	short nasal bone	J:58700
skin hemorrhage	J:58700
transposition of great arteries	J:80720, J:107987
Hspg2tm1Ref/Hspg2tm1Ref involves: 129S1/Sv * 129X1/SvJ * C57BL/6	abnormal basement membrane morphology	J:119018
	abnormal radial glial cell endfoot morphology	J:119018
	exencephaly	J:119018
Hspg2tm1Soin/Hspg2tm1Soin B6.129P2-Hspg2tm1Soin	normal homeostasis/metabolism phenotype	J:167008
Hspg2tm1Soni/Hspg2tm1Soni involves: 129S/SvEv * C57BL/6	abnormal behavior	J:139975
	decreased body weight	J:139975
	delayed eyelid opening	J:139975
	normal mortality/aging	J:139975
Hspg2tm1Soni/Hspg2tm1Soni involves: 129S/SvEv * DBA/2J	abnormal action potential	J:183547
	abnormal axon morphology	J:183547
	abnormal internode morphology	J:183547
	abnormal myelin sheath morphology	J:183547
	abnormal neuromuscular synapse morphology	J:183547
	abnormal node of Ranvier morphology	J:183547
	abnormal paranode morphology	J:183547
	demyelination	J:183547
	increased Schwann cell number	J:183547