52 phenotypes from 6 alleles in 6 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Diaph3tm1.1Pji/Diaph3tm1.1Pji Tg(Mx1-cre)1Cgn/0 involves: C57BL/6J * CBA/J	abnormal erythropoiesis	J:293763
	anemia	J:293763
	anisopoikilocytosis	J:293763
	decreased erythrocyte cell number	J:293763
	decreased hematocrit	J:293763
	decreased hemoglobin content	J:293763
	enlarged spleen	J:293763
	extramedullary hematopoiesis	J:293763
	increased red blood cell distribution width	J:293763
	polychromatophilia	J:293763
Diaph3tm1.1Sna/Diaph3tm1.1Sna B6NSlc.Cg-Diaph3tm1.1Sna	abnormal cell cycle	J:205519
	abnormal nucleated erythrocyte cell number	J:205519
	normal cardiovascular system phenotype	J:205519
	decreased embryo size	J:205519
	decreased erythroblast number	J:205519
	embryonic lethality during organogenesis, complete penetrance	J:205519
	extramedullary hematopoiesis	J:205519
Diaph3tm1.2Pji/Diaph3tm1.2Pji Not Specified	embryonic lethality during organogenesis, complete penetrance	J:293763
Diaph3tm1b(KOMP)Mbp/Diaph3+ C57BL/6N-Diaph3tm1b(KOMP)Mbp/J	abnormal cornea morphology	J:211773
	abnormal eyelid morphology	J:211773
	abnormal iris morphology	J:211773
	abnormal iris pigmentation	J:211773
	abnormal iris transillumination	J:211773
	abnormal placement of pupils	J:211773
	corneal deposits	J:211773
	corneal opacity	J:211773
	corneal vascularization	J:211773
	decreased circulating free fatty acids level	J:211773
	decreased circulating triglyceride level	J:211773
	decreased mean corpuscular volume	J:211773
	exophthalmos	J:211773
	eye hemorrhage	J:211773
	eyelids fail to open	J:211773
	impaired pupillary reflex	J:211773
	increased mean corpuscular hemoglobin concentration	J:211773
	irregularly shaped pupil	J:211773
	mydriasis	J:211773
	narrow eye opening	J:211773
	sclerocornea	J:211773
Diaph3tm1b(KOMP)Mbp/Diaph3tm1b(KOMP)Mbp C57BL/6N-Diaph3tm1b(KOMP)Mbp/J	abnormal craniofacial morphology	J:211773
	abnormal embryo size	J:211773
	abnormal embryo turning	J:211773
	abnormal pericardium morphology	J:211773
	embryonic growth retardation	J:211773
	pallor	J:211773
	preweaning lethality, complete penetrance	J:211773
Tg(CAG-Diap3)924Lesp/0 FVB/NJ-Tg(CAG-Diap3)924Lesp	abnormal cardiovascular system morphology	J:193237
	abnormal inner hair cell stereociliary bundle morphology	J:193237
	abnormal inner hair cell synaptic ribbon morphology	J:193237
	normal behavior/neurological phenotype	J:193237
	decreased inner hair cell stereocilia number	J:193237
	impaired hearing	J:193237
	increased or absent threshold for auditory brainstem response	J:193237
	premature death	J:193237
Tg(CAG-Diaph3)771Lesp/0 FVB/NJ-Tg(CAG-Diaph3)771Lesp	abnormal cardiovascular system morphology	J:193237
	abnormal inner hair cell stereociliary bundle morphology	J:193237
	abnormal inner hair cell synaptic ribbon morphology	J:193237
	normal behavior/neurological phenotype	J:193237
	decreased inner hair cell stereocilia number	J:193237
	impaired hearing	J:193237
	increased or absent threshold for auditory brainstem response	J:193237
	premature death	J:193237