34 phenotypes from 2 alleles in 3 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Ripk4tm1a(EUCOMM)Wtsi/Ripk4+ C57BL/6N-Ripk4tm1a(EUCOMM)Wtsi/Wtsi	decreased body weight	J:175295
Ripk4tm1Pmh/Ripk4tm1Pmh involves: 129	normal craniofacial phenotype	J:184926
Ripk4tm1Pmh/Ripk4tm1Pmh involves: 129 * C57BL/6	abnormal actin cytoskeleton morphology	J:259661
	abnormal epidermis suprabasal layer morphology	J:78593
	abnormal forelimb morphology	J:259661
	abnormal genital tubercle morphology	J:259661
	abnormal hindlimb morphology	J:78593, J:259661
	abnormal keratinocyte differentiation	J:78593, J:259661
	abnormal nose morphology	J:78593
	abnormal periderm development	J:259661
	abnormal periderm morphology	J:259661
	abnormal secondary palate development	J:259661
	abnormal skin appearance	J:78593
	abnormal tail morphology	J:78593
	abnormal vibrissa morphology	J:78593
	absent epidermis stratum corneum	J:78593
	absent vibrissae	J:78593
	anal atresia	J:78593
	cleft palate	J:259661
	epidermal hyperplasia	J:78593
	esophageal atresia	J:78593, J:259661
	failure of palatal shelf elevation	J:259661
	normal hematopoietic system phenotype	J:78593
	normal immune system phenotype	J:78593
	impaired skin barrier function	J:259661
	interdigital webbing	J:78593
	oral atresia	J:78593, J:259661
	palatal shelf fusion with tongue or mandible	J:259661
	parakeratosis	J:78593
	perinatal lethality, complete penetrance	J:78593
	short hindlimb	J:78593
	short tail	J:78593
	thick epidermis	J:78593
	thick skin	J:78593