79 phenotypes from 3 alleles in 3 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Ankrd11tm1b(EUCOMM)Wtsi/Ankrd11+ C57BL/6N-Ankrd11tm1b(EUCOMM)Wtsi/Ics	abnormal auditory brainstem response	J:211773
	abnormal startle reflex	J:211773
	abnormal vitreous body morphology	J:211773
	decreased body length	J:211773
	decreased prepulse inhibition	J:211773
	decreased startle reflex	J:211773
	increased circulating cholesterol level	J:211773
	increased circulating HDL cholesterol level	J:211773
Ankrd11tm1b(EUCOMM)Wtsi/Ankrd11tm1b(EUCOMM)Wtsi C57BL/6N-Ankrd11tm1b(EUCOMM)Wtsi/Ics	abnormal embryo development	J:211773
	preweaning lethality, complete penetrance	J:211773
Ankrd11tm1c(EUCOMM)Wtsi/Ankrd11+ E2f1Tg(Wnt1-cre)2Sor/E2f1+ involves: C3H * C57BL/6 * C57BL/6N	abnormal frontal bone morphology	J:306391
	abnormal mandible morphology	J:306391
	abnormal midface morphology	J:306391
	abnormal neurocranium morphology	J:306391
	abnormal nose morphology	J:306391
	abnormal pterygoid bone morphology	J:306391
	enlarged neurocranium	J:306391
	large anterior fontanelle	J:306391
	midface hypoplasia	J:306391
	normal mortality/aging	J:306391
	narrow face	J:306391
	wide metopic suture	J:306391
Ankrd11tm1c(EUCOMM)Wtsi/Ankrd11tm1c(EUCOMM)Wtsi E2f1Tg(Wnt1-cre)2Sor/E2f1+ involves: C3H * C57BL/6 * C57BL/6N	abnormal basicranium morphology	J:306391
	abnormal bone collagen fibril morphology	J:306391
	abnormal bone remodeling	J:306391
	abnormal cranial blood vasculature morphology	J:306391
	abnormal craniofacial morphology	J:306391
	abnormal head morphology	J:306391
	abnormal intramembranous bone ossification	J:306391
	abnormal neurocranium morphology	J:306391
	abnormal osteocyte morphology	J:306391
	abnormal palatal mesenchymal cell proliferation	J:306391
	abnormal palatal shelf morphology	J:306391
	abnormal palatine bone morphology	J:306391
	abnormal snout skin morphology	J:306391
	absent pterygoid process	J:306391
	cleft hard palate	J:306391
	cleft palate	J:306391
	decreased bone ossification	J:306391
	decreased bone resorption	J:306391
	decreased bone trabecula number	J:306391
	decreased osteoclast cell number	J:306391
	decreased tongue size	J:306391
	delayed intramembranous bone ossification	J:306391
	domed cranium	J:306391
	eyelids open at birth	J:306391
	frontal bone hypoplasia	J:306391
	hypopigmentation	J:306391
	impaired ossification of basisphenoid bone	J:306391
	large anterior fontanelle	J:306391
	micrognathia	J:306391
	midface hypoplasia	J:306391
	palatal shelf hypoplasia	J:306391
	palatal shelves fail to meet at midline	J:306391
	perinatal lethality, complete penetrance	J:306391
	retrognathia	J:306391
	short tongue	J:306391
	small frontal bone	J:306391
	small mandible	J:306391
	small parietal bone	J:306391
	tongue hypoplasia	J:306391
	triangular face	J:306391
Ankrd11Yod/Ankrd11+ involves: BALB/cAnNCrl * C3H/HeH	abnormal bone structure	J:136455
	abnormal craniofacial bone morphology	J:136455
	abnormal frontonasal suture morphology	J:136455
	abnormal metopic suture morphology	J:136455
	abnormal nasal bone morphology	J:136455
	broad face	J:136455
	decreased body length	J:136455
	decreased body weight	J:136455
	decreased bone mass	J:136455
	decreased bone mineral density of femur	J:136455
	decreased circulating leptin level	J:136455
	decreased compact bone area	J:136455
	decreased osteoclast cell number	J:136455
	domed cranium	J:136455
	enlarged parietal bone	J:136455
	increased cranium width	J:136455
	kyphosis	J:136455
	short face	J:136455
	short frontal bone	J:136455
	short nasal bone	J:136455
Ankrd11Yod/Ankrd11Yod involves: BALB/cAnNCrl * C3H/HeH	decreased embryo size	J:136455
	embryonic lethality during organogenesis, complete penetrance	J:136455
	failure of initiation of embryo turning	J:136455