35 phenotypes from 3 alleles in 3 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Flncem1(IMPC)Bay/Flnc+ C57BL/6N-Flncem1(IMPC)Bay/BayMmucd	decreased exploration in new environment	J:211773
Flncem1(IMPC)Bay/Flncem1(IMPC)Bay C57BL/6N-Flncem1(IMPC)Bay/BayMmucd	abnormal heart looping	J:211773
	abnormal heart morphology	J:211773
	abnormal somite shape	J:211773
	abnormal vitelline vasculature morphology	J:211773
	embryonic lethality prior to tooth bud stage	J:211773
	preweaning lethality, complete penetrance	J:211773
Flnctm1.1Rsdf/Flnc+ involves: C57BL/6	abnormal muscle fiber morphology	J:226976
	abnormal sarcomere morphology	J:226976
	abnormal Z line morphology	J:226976
	decreased food intake	J:226976
	decreased grip strength	J:226976
	decreased locomotor activity	J:226976
	decreased respiratory quotient	J:226976
	decreased vertical activity	J:226976
	normal muscle phenotype	J:226976
	skeletal muscle fiber degeneration	J:226976
Flnctm1.1Rsdf/Flnctm1.1Rsdf involves: C57BL/6	normal mortality/aging	J:226976
Flnctm1Lmk/Flnctm1Lmk involves: 129X1/SvJ * C57BL/6	abnormal diaphragm morphology	J:112170
	abnormal extensor digitorum longus morphology	J:112170
	abnormal intercostal muscle morphology	J:112170
	abnormal myogenesis	J:112170
	abnormal skeletal muscle fiber morphology	J:112170
	abnormal skeletal muscle morphology	J:112170
	abnormal soleus morphology	J:112170
	abnormal tibialis anterior morphology	J:112170
	normal cardiovascular system phenotype	J:112170
	centrally nucleated skeletal muscle fibers	J:112170
	decreased fetal size	J:112170
	decreased skeletal muscle fiber number	J:112170
	decreased skeletal muscle mass	J:112170
	hyporesponsive to tactile stimuli	J:112170
	increased variability of skeletal muscle fiber size	J:112170
	neonatal lethality, complete penetrance	J:112170
	respiratory failure	J:112170