105 phenotypes from 9 alleles in 11 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Bmp7tm1.1Dgra/Bmp7tm1.1Dgra B6.Cg-Bmp7tm1.1Dgra	no abnormal phenotype detected	J:149134
Bmp7tm1.1Dgra/Bmp7tm1.1Dgra H2az2Tg(Wnt1-cre)11Rth/H2az2+ involves: 129S6/SvEvTac * C57BL/6J * C57BL/6NTac * CBA/J	abnormal basicranium angle	J:302309
	abnormal basisphenoid bone morphology	J:302309
	abnormal face development	J:302309
	abnormal nasal bone morphology	J:302309
	abnormal neurocranium morphology	J:302309
	abnormal respiration	J:302309
	abnormal snout morphology	J:302309
	abnormal turbinate morphology	J:302309
	apnea	J:302309
	decreased body temperature	J:302309
	decreased oxygen consumption	J:302309
	decreased pulmonary respiratory rate	J:302309
	deviated nasal septum	J:302309
	frontal bossing	J:302309
	impaired exercise endurance	J:302309
	increased circulating hydroxyproline level	J:302309
	midface hypoplasia	J:302309
	nasal obstruction	J:302309
	premature death	J:302309
	short basicranium	J:302309
	short nasal bone	J:302309
Bmp7tm1.1Dgra/Bmp7tm1.1Dgra Tg(Prrx1-cre)1Cjt/0 involves: 129S6/SvEvTac * C57BL/6J * C57BL/6NTac * SJL/J	abnormal cartilage morphology	J:221175
	abnormal joint morphology	J:221175
	joint inflammation	J:221175
	osteoarthritis	J:221175
Bmp7tm1.2Dgra/Bmp7tm1.2Dgra B6.Cg-Bmp7tm1.2Dgra	abnormal basioccipital bone morphology	J:148972
	abnormal cochlea morphology	J:148972
	abnormal craniofacial development	J:148972
	abnormal craniofacial morphology	J:148972
	abnormal cranium morphology	J:148972
	abnormal cricoid cartilage morphology	J:148972
	abnormal hair follicle morphology	J:148972
	abnormal hard palate morphology	J:148972
	abnormal hyoid bone morphology	J:148972
	abnormal lower incisor morphology	J:148972
	abnormal mandible morphology	J:148972
	abnormal maxilla morphology	J:148972
	abnormal maxillary shelf morphology	J:148972
	abnormal middle ear ossicle morphology	J:148972
	abnormal molar morphology	J:148972
	abnormal nasal capsule morphology	J:148972
	abnormal nasal septum cartilage morphology	J:148972
	abnormal semicircular canal morphology	J:148972
	abnormal soft palate morphology	J:148972
	abnormal temporal bone petrous part morphology	J:148972
	abnormal thyroid cartilage morphology	J:148972
	abnormal tooth morphology	J:148972
	abnormal vibrissa morphology	J:148972
	abnormal vibrissa number	J:148972
	absent cricoid cartilage	J:148972
	absent thyroid cartilage	J:148972
	absent upper incisors	J:148972
	anophthalmia	J:148972
	cleft palate	J:148972
	decreased molar number	J:148972
	exencephaly	J:148972
	growth retardation of molars	J:148972
	hair follicle outer root sheath hyperplasia	J:148972
	palatal shelf hypoplasia	J:148972
	palatal shelves fail to meet at midline	J:148972
	small Meckel's cartilage	J:148972
Bmp7tm1.2Dgra/Bmp7tm1.2Dgra involves: 129S4/SvJae * 129S6/SvEvTac * BALB/cJ * C57BL/6J * C57BL/6NTac	abnormal eye development	J:149134
	abnormal kidney mesenchyme morphology	J:149134
	abnormal lens vesicle development	J:149134
	abnormal renal glomerulus morphology	J:149134
	abnormal sternum morphology	J:149134
	anophthalmia	J:149134
	decreased fetal size	J:149134
	dilated renal glomerular capsule	J:149134
	microphthalmia	J:149134
	polydactyly	J:149134
	preweaning lethality, complete penetrance	J:149134
	renal hypoplasia	J:149134
	retina pigment epithelium atrophy	J:149134
	rib bifurcation	J:149134
	rib fusion	J:149134
	short rostral-caudal axis	J:149134
Bmp7tm1a(EUCOMM)Hmgu/Bmp7+ C57BL/6N-Bmp7tm1a(EUCOMM)Hmgu/H	decreased erythrocyte cell number	J:165965
	increased mean corpuscular volume	J:165965
	increased monocyte cell number	J:165965
Bmp7tm1Kry/Bmp7tm1Kry involves: 129S7/SvEvBrd * C57BL/6	abnormal alisphenoid bone morphology	J:30056
	abnormal apical ectodermal ridge morphology	J:35171
	abnormal basisphenoid bone morphology	J:30056
	abnormal digit morphology	J:35171
	abnormal lens vesicle development	J:30056
	abnormal xiphoid process morphology	J:30056
	absent metanephric mesenchyme	J:30056
	anophthalmia	J:30056
	aphakia	J:30056
	asymmetric sternocostal joints	J:30056
	basisphenoid bone foramen	J:30056
	broad limb buds	J:35171
	decreased body size	J:30056
	decreased body weight	J:30056
	decreased renal glomerulus number	J:30056
	decreased rib number	J:30056
	hydroureter	J:30056
	polydactyly	J:30056
	postnatal lethality, complete penetrance	J:30056
	rib fusion	J:30056
	normal skeleton phenotype	J:30056
	small basisphenoid bone	J:30056
	small kidney	J:30056
	small pterygoid bone	J:30056
Bmp7tm1Kry/Bmp7tm1Kry Not Specified	normal cardiovascular system phenotype	J:89237
Bmp7tm1Rob/Bmp7tm1Rob 129S-Bmp7tm1Rob	abnormal axial skeleton morphology	J:30057
	abnormal cranium morphology	J:30057
	abnormal kidney development	J:30057
	abnormal sternocostal joint morphology	J:30057
	anophthalmia	J:30057
	exencephaly	J:30057
	hydroureter	J:30057
	microphthalmia	J:30057
	neonatal lethality, incomplete penetrance	J:30057
	polydactyly	J:30057
Bmp7tm1Rob/Bmp7tm1Rob either: (involves: 129S/SvEv * C57BL/6J) or (involves: 129S/SvEv * MF1)	abnormal axial skeleton morphology	J:30057
	abnormal cranium morphology	J:30057
	abnormal kidney development	J:30057
	abnormal sternocostal joint morphology	J:30057
	anophthalmia	J:30057
	exencephaly	J:30057
	hydroureter	J:30057
	microphthalmia	J:30057
	neonatal lethality, incomplete penetrance	J:30057
	polydactyly	J:30057
Bmp7tm2Rob/Bmp7tm2Rob involves: 129S/SvEv	abnormal kidney development	J:103587
	hydroureter	J:103587
	kidney cyst	J:103587
Bmp7tm2Rob/Bmp7tm4(Bmp4)Rob involves: 129S/SvEv	microphthalmia	J:103587
Bmp7tm2Rob/Bmp7tm5(Bmp7/Bmp6)Rob involves: 129S/SvEv	no abnormal phenotype detected	J:103587
Bmp7tm3(Bmp7)Rob/Bmp7tm2Rob involves: 129S/SvEv	no abnormal phenotype detected	J:103587