42 phenotypes from 5 alleles in 6 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Myo10m1J/Myo10m1J B6.Cg-Myo10m1J/GrsrJ	abnormal eye morphology	J:214794
	abnormal tail pigmentation	J:214794
	belly spot	J:214794
	cornea opacity	J:214794
	decreased body size	J:214794
	decreased tail pigmentation	J:214794
	fused phalanges	J:214794
	iris coloboma	J:214794
	persistence of hyaloid vascular system	J:214794
	syndactyly	J:214794
	white spotting	J:214794
Myo10m1J/Myo10m1J involves: C57BL/6J	abnormal brain morphology	J:256438
	abnormal lens development	J:256438
	absent liver	J:256438
	acrania	J:256438
	anophthalmia	J:256438
	normal behavior/neurological phenotype	J:256438
	belly spot	J:256438
	craniorachischisis	J:256438
	decreased body weight	J:256438
	decreased embryo size	J:256438
	decreased survivor rate	J:256438
	exencephaly	J:256438
	failure of eyelid fusion	J:256438
	hemorrhage	J:256438
	lethality during fetal growth through weaning, incomplete penetrance	J:256438
	microphthalmia	J:256438
	persistence of hyaloid vascular system	J:256438
	syndactyly	J:256438
	white spotting	J:256438
Myo10tm1a(KOMP)Wtsi/Myo10tm1a(KOMP)Wtsi involves: C57BL/6N	belly spot	J:256438
	decreased survivor rate	J:256438
	exencephaly	J:256438
	kinked tail	J:256438
	lethality during fetal growth through weaning, incomplete penetrance	J:256438
	persistence of hyaloid vascular system	J:256438
	syndactyly	J:256438
	white spotting	J:256438
Myo10tm1c(KOMP)Wtsi/Myo10tm1c(KOMP)Wtsi involves: C57BL/6 * C57BL/6N	no abnormal phenotype detected	J:256438
Myo10tm1d(KOMP)Wtsi/Myo10tm1d(KOMP)Wtsi involves: C57BL/6 * C57BL/6N * C57BL/6NJ	abnormal retina morphology	J:256438
	abnormal retina vasculature morphology	J:256438
	abnormal vascular branching morphogenesis	J:256438
	anophthalmia	J:256438
	normal behavior/neurological phenotype	J:256438
	belly spot	J:256438
	decreased body weight	J:256438
	decreased survivor rate	J:256438
	exencephaly	J:256438
	kinked tail	J:256438
	lethality during fetal growth through weaning, incomplete penetrance	J:256438
	microphthalmia	J:256438
	persistence of hyaloid vascular system	J:256438
	syndactyly	J:256438
	white spotting	J:256438
Myo10tm2(KOMP)Wtsi/Myo10tm2(KOMP)Wtsi C57BL/6N-Myo10tm2(KOMP)Wtsi/Wtsi	abnormal coat/hair pigmentation	J:211773
	abnormal cornea morphology	J:211773
	abnormal digit morphology	J:211773
	abnormal iris morphology	J:211773
	abnormal lens morphology	J:211773
	abnormal response to new environment	J:211773
	abnormal retina morphology	J:211773
	abnormal tail morphology	J:211773
	cataract	J:211773
	cornea opacity	J:211773
	decreased circulating creatinine level	J:211773
	fused cornea and lens	J:211773
	fused phalanges	J:211773
	impaired pupillary reflex	J:211773
	persistence of hyaloid vascular system	J:211773