57 phenotypes from 3 alleles in 2 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
HhatTg(TFAP2A-cre)1Will/HhatTg(TFAP2A-cre)1Will Not Specified	abnormal cartilage development	J:190013
	abnormal cranium morphology	J:190013
	abnormal eye development	J:190013
	abnormal fetal Leydig cell differentiation	J:226657
	abnormal forebrain morphology	J:190013
	abnormal mandible morphology	J:190013
	abnormal mandibular prominence morphology	J:190013
	abnormal maxillary prominence morphology	J:190013
	abnormal midbrain morphology	J:190013
	abnormal nasal cartilage morphology	J:190013
	abnormal nasal cavity morphology	J:190013
	abnormal neural crest cell morphology	J:190013
	abnormal neural crest morphology	J:190013
	abnormal optic vesicle formation	J:190013
	abnormal oral cavity morphology	J:190013
	abnormal palatal shelf elevation	J:190013
	abnormal palatal shelf fusion at midline	J:190013
	abnormal palate development	J:190013
	abnormal testis cord formation	J:226657
	abnormal testis development	J:226657
	abnormal testis morphology	J:226657
	abnormal vertebral column morphology	J:190013
	absent cornea	J:190013
	absent interparietal bone	J:190013
	absent mandibular angle	J:190013
	absent mandibular condyloid process	J:190013
	absent mandibular coronoid process	J:190013
	absent nasal septum	J:190013
	absent parietal bone	J:190013
	absent supraoccipital bone	J:190013
	absent tooth placode	J:190013
	acrania	J:190013
	agnathia	J:190013
	arrest of tooth development	J:190013
	decreased embryo size	J:190013
	diencephalon hypoplasia	J:190013
	edema	J:190013
	failure of bone ossification	J:190013
	hemorrhage	J:190013
	microphthalmia	J:190013
	nasal cartilage hypoplasia	J:190013
	oligodactyly	J:190013
	prenatal lethality, complete penetrance	J:190013
	small basioccipital bone	J:190013
	small embryonic telencephalon	J:190013
	small exoccipital bone	J:190013
	small frontonasal prominence	J:190013
	small testis	J:226657
	tongue hypoplasia	J:190013
Hhattm1Ptch/Hhattm1Ptch involves: 129P2/OlaHsd * FVB/N * various	abnormal ventral interneuron 2 morphology	J:89228
	abnormal ventral interneuron 3 morphology	J:89228
	absent floor plate	J:89228
	chondrodystrophy	J:89228
	decreased embryo size	J:89228
	decreased motor neuron number	J:89228
	disproportionate dwarf	J:89228
	holoprosencephaly	J:89228
	neonatal lethality, complete penetrance	J:89228
	oligodactyly	J:89228
Hhattm2Ptch/Hhattm2Ptch involves: 129P2/OlaHsd * FVB/N * various	abnormal ventral interneuron 2 morphology	J:89228
	abnormal ventral interneuron 3 morphology	J:89228
	absent floor plate	J:89228
	chondrodystrophy	J:89228
	decreased embryo size	J:89228
	decreased motor neuron number	J:89228
	disproportionate dwarf	J:89228
	holoprosencephaly	J:89228
	neonatal lethality, complete penetrance	J:89228
	oligodactyly	J:89228