35 phenotypes from 2 alleles in 3 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Ovol1tm1b(KOMP)Wtsi/Ovol1+ C57BL/6N-Ovol1tm1b(KOMP)Wtsi/J	abnormal coat/hair pigmentation	J:211773
	abnormal vibrissa morphology	J:211773
	decreased erythrocyte cell number	J:211773
	decreased hematocrit	J:211773
	decreased hemoglobin content	J:211773
	thrombocytopenia	J:211773
Ovol1tm1Efu/Ovol1+ B6.129-Ovol1tm1Efu	kidney cyst	J:118154
Ovol1tm1Efu/Ovol1tm1Efu B6.129-Ovol1tm1Efu	impaired skin barrier function	J:118154
	kidney cyst	J:118154
	lethality throughout fetal growth and development, incomplete penetrance	J:118154
	postnatal lethality, incomplete penetrance	J:118154
Ovol1tm1Efu/Ovol1tm1Efu involves: 129S1/Sv * 129X1/SvJ * C57BL/6	abnormal auchene hair morphology	J:50844
	abnormal awl hair morphology	J:50844
	abnormal hair shaft morphology	J:50844
	abnormal kidney morphology	J:50844
	abnormal skin condition	J:50844
	abnormal spermatogenesis	J:50844
	abnormal testis morphology	J:50844
	constricted vagina orifice	J:50844
	decreased body size	J:50844
	decreased body weight	J:50844
	decreased male germ cell number	J:50844
	decreased testis weight	J:50844
	dilated uterine cervix	J:50844
	dilated uterus	J:50844
	kidney atrophy	J:50844
	kidney cortex cyst	J:50844
	kidney cyst	J:50844
	normal mortality/aging	J:118154
	reduced female fertility	J:50844
	reduced male fertility	J:50844
	ruffled hair	J:50844
	seminiferous tubule degeneration	J:50844
	small seminiferous tubules	J:50844
	small testis	J:50844
	splitting of guard hairs	J:50844
	vagina atresia	J:50844