31 phenotypes from 6 alleles in 5 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Kdm8Gt(AZ0518)Wtsi/Kdm8Gt(AZ0518)Wtsi involves: 129P2/OlaHsd * C57BL/6	abnormal embryo turning	J:182585
	decreased embryo size	J:182585
	embryonic growth retardation	J:182585
	embryonic lethality during organogenesis, complete penetrance	J:182585
	open neural tube	J:182585
Kdm8tm1.1Tasu/Kdm8tm1.1Tasu involves: 129S4/SvJae * C57BL/6	no abnormal phenotype detected	J:181189
Kdm8tm1.2Tasu/Kdm8tm1.2Tasu involves: 129S4/SvJae * C3H * C57BL/6	abnormal visceral yolk sac morphology	J:181189
	absent vitelline blood vessels	J:181189
	embryonic growth retardation	J:181189
	embryonic lethality during organogenesis, complete penetrance	J:181189
	incomplete embryo turning	J:181189
Kdm8tm1a(EUCOMM)Wtsi/Kdm8+ C57BL/6N-Kdm8tm1a(EUCOMM)Wtsi/Ics	abnormal glucose homeostasis	J:165965
	abnormal iris pigmentation	J:165965
	abnormal response to tactile stimuli	J:165965
	increased B cell number	J:165965
	increased body weight	J:165965
Kdm8tm1b(EUCOMM)Wtsi/Kdm8+ C57BL/6N-Kdm8tm1b(EUCOMM)Wtsi/Ics	abnormal behavior	J:211773
	abnormal iris morphology	J:211773
	abnormal lens morphology	J:211773
	abnormal optic disk morphology	J:211773
	abnormal retina blood vessel morphology	J:211773
	abnormal retina vasculature morphology	J:211773
	cataract	J:211773
	corneal vascularization	J:211773
	fused cornea and lens	J:211773
	impaired pupillary reflex	J:211773
	iris synechia	J:211773
	mydriasis	J:211773
Kdm8tm1b(EUCOMM)Wtsi/Kdm8tm1b(EUCOMM)Wtsi C57BL/6N-Kdm8tm1b(EUCOMM)Wtsi/Ics	embryonic lethality prior to tooth bud stage	J:211773
	preweaning lethality, complete penetrance	J:211773
Kdm8tm1Tasu/Kdm8tm1Tasu involves: 129S4/SvJae * C57BL/6	decreased cell proliferation	J:181189
	decreased embryo size	J:181189
	embryonic growth retardation	J:181189
	embryonic lethality during organogenesis, incomplete penetrance	J:181189
	prenatal lethality	J:181189
	preweaning lethality, complete penetrance	J:181189