80 phenotypes from 7 alleles in 9 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Irf6clft1/Irf6clft1 involves: A/J * FVB	abnormal hindlimb morphology	J:160190
	abnormal mouth morphology	J:160190
	abnormal palatine bone horizontal plate morphology	J:160190
	abnormal skeleton morphology	J:160190
	cleft secondary palate	J:160190
	curly tail	J:160190
	delayed skin barrier formation	J:160190
	failure of palatal shelf elevation	J:160190
	fused phalanges	J:160190
	glossopalatal ankylosis	J:160190
	palatal shelf fusion with tongue or mandible	J:160190
	short forelimb	J:160190
	syndactyly	J:160190
Irf6em1(IMPC)Wtsi/Irf6em1(IMPC)Wtsi C57BL/6N-Irf6em1(IMPC)Wtsi/Wtsi	increased circulating aspartate transaminase level	J:211773
	increased circulating creatine kinase level	J:211773
	increased circulating creatinine level	J:211773
Irf6Gt(OST398253)Lex/Irf6+ involves: 129S5/SvEvBrd * C57BL/6	abnormal craniofacial development	J:226218
	abnormal periderm development	J:226218
Irf6Gt(OST398253)Lex/Irf6Gt(OST398253)Lex involves: 129S5/SvEvBrd	abnormal skin development	J:180634
	failure of palatal shelf elevation	J:160190
	palatal shelf fusion with tongue or mandible	J:160190
Irf6Gt(OST398253)Lex/Irf6Gt(OST398253)Lex involves: 129S5/SvEvBrd * C57BL/6	abnormal cranium morphology	J:115343
	abnormal digit morphology	J:115343
	abnormal epidermal layer morphology	J:115343
	abnormal epidermis stratum spinosum morphology	J:115343
	abnormal esophagus morphology	J:115343
	abnormal jaw morphology	J:115343
	abnormal keratinocyte differentiation	J:115343
	abnormal mandibular angle morphology	J:115343
	abnormal oral cavity morphology	J:226218
	abnormal palate development	J:226218
	abnormal periderm development	J:226218
	abnormal phalanx morphology	J:115343
	absent epidermis stratum corneum	J:115343
	absent epidermis stratum granulosum	J:115343
	absent outer ear	J:115343
	absent presphenoid bone	J:115343
	cleft palate	J:226218
	cleft secondary palate	J:115343
	decreased length of long bones	J:115343
	delayed bone ossification	J:115343
	increased keratinocyte proliferation	J:115343
	perinatal lethality, complete penetrance	J:94918
	round snout	J:115343
	shiny skin	J:115343
	short forelimb	J:115343
	short snout	J:115343
	short sternum	J:115343
	short tail	J:115343
	small mandible	J:115343
	small vertebrae	J:115343
	split xiphoid process	J:115343
	synostosis	J:115343
	thick epidermis	J:115343
	tight skin	J:115343
Irf6tm1.1Bcsl/Irf6tm1.1Bcsl Not Specified	abnormal skin development	J:180634
Irf6tm1Bcsl/Irf6tm1Bcsl Pitx2tm4(cre)Jfm/Pitx2+ involves: 129	abnormal ameloblast morphology	J:275989
	abnormal enamel development	J:275989
	abnormal enamel mineralization	J:275989
	abnormal enamel morphology	J:275989
	abnormal enamel rod pattern	J:275989
	abnormal Hertwig epithelial root sheath morphology	J:275989
	abnormal incisor color	J:275989
	abnormal incisor morphology	J:275989
	abnormal molar crown morphology	J:275989
	abnormal molar cusp morphology	J:275989
	abnormal molar morphology	J:275989
	abnormal molar root morphology	J:275989
	abnormal tooth morphology	J:275989
	decreased molar number	J:275989
	reduced enamel thickness	J:275989
	supernumerary teeth	J:275989
	taurodontia	J:275989
Irf6tm1Mjd/Irf6+ involves: 129S1/Sv * 129X1/SvJ * C57BL/6	abnormal mouth morphology	J:116077
	neonatal lethality, incomplete penetrance	J:116077
Irf6tm1Mjd/Irf6tm1Mjd involves: 129S1/Sv * 129X1/SvJ	abnormal craniofacial development	J:184926
	abnormal incisor morphology	J:184926
	abnormal tooth development	J:184926
	failure of palatal shelf elevation	J:160190
	palatal shelf fusion with tongue or mandible	J:160190
Irf6tm1Mjd/Irf6tm1Mjd involves: 129S1/Sv * 129X1/SvJ * C57BL/6	abnormal craniofacial bone morphology	J:116077
	abnormal digit development	J:116077
	abnormal epidermal layer morphology	J:116077
	abnormal epidermis stratum basale morphology	J:116077
	abnormal epidermis suprabasal layer morphology	J:116077
	abnormal esophagus development	J:116077
	abnormal keratinocyte morphology	J:116077
	absent epidermis stratum corneum	J:116077
	absent epidermis stratum granulosum	J:116077
	absent vibrissae	J:116077
	cleft secondary palate	J:116077
	decreased hair follicle number	J:116077
	palatal shelf fusion with tongue or mandible	J:116077
	postnatal lethality, complete penetrance	J:116077
	shiny skin	J:116077
	short limbs	J:116077
	short tail	J:116077
	thick epidermis	J:116077
Irf6tm1Mjd/Irf6tm1Pts involves: 129S1/Sv * 129X1/SvJ * C57BL/6	normal craniofacial phenotype	J:184926
Irf6tm1Pts/Irf6tm1Pts involves: 129 * C57BL/6	normal craniofacial phenotype	J:184926