90 phenotypes from multigenic genotypes

Allelic Composition Genetic Background	Annotated Term	Reference
Bmp2tm1Brd/Bmp2+ Bmp7tm1Kry/Bmp7+ Not Specified	normal skeleton phenotype	J:48538
Bmp2tm1Cjt/Bmp2+ Bmp7tm1Rob/Bmp7+ Tg(Prrx1-cre)1Cjt/0 involves: 129S/SvEv * C57BL/6 * SJL	no abnormal phenotype detected	J:118257
Bmp2tm1Cjt/Bmp2+ Bmp7tm1Rob/Bmp7tm1Rob Tg(Prrx1-cre)1Cjt/0 involves: 129S/SvEv * C57BL/6 * SJL	no abnormal phenotype detected	J:118257
Bmp2tm1Cjt/Bmp2tm1Cjt Bmp7tm1Rob/Bmp7+ Tg(Prrx1-cre)1Cjt/0 involves: 129S/SvEv * C57BL/6 * SJL	abnormal scapula morphology	J:118257
Bmp2tm1Cjt/Bmp2tm1Cjt Bmp7tm1Rob/Bmp7tm1Rob Tg(Prrx1-cre)1Cjt/0 involves: 129S/SvEv * C57BL/6 * SJL	abnormal appendicular skeleton morphology	J:118257
	abnormal fibula morphology	J:118257
	abnormal phalanx morphology	J:118257
	abnormal scapula morphology	J:118257
Bmp2tm1Jfm/Bmp2+ Bmp4tm1Jfm/Bmp4+ Bmp7tm1Jfm/Bmp7tm1Jfm H2az2Tg(Wnt1-cre)11Rth/H2az2+ involves: 129S4/SvJaeSor * C57BL/6J * CBA/J	absent alisphenoid bone	J:181229
	cleft palate	J:181229
	decreased tympanic ring size	J:181229
	small temporal bone squamous part	J:181229
Bmp2tm1Jfm/Bmp2+ Bmp4tm1Jfm/Bmp4tm1Jfm Bmp7tm1Jfm/Bmp7+ H2az2Tg(Wnt1-cre)11Rth/H2az2+ involves: 129S4/SvJaeSor * C57BL/6J * CBA/J	cleft palate	J:181229
	decreased tympanic ring size	J:181229
	small alisphenoid bone	J:181229
	small nasal bone	J:181229
	small temporal bone squamous part	J:181229
	small zygomatic bone	J:181229
Bmp2tm1Jfm/Bmp2+ Bmp4tm1Jfm/Bmp4tm1Jfm Bmp7tm1Jfm/Bmp7tm1Jfm H2az2Tg(Wnt1-cre)11Rth/H2az2+ involves: 129S4/SvJaeSor * C57BL/6J * CBA/J	abnormal tympanic ring morphology	J:181229
	cleft palate	J:181229
	small interparietal bone	J:181229
	small nasal bone	J:181229
	small temporal bone squamous part	J:181229
	small zygomatic bone	J:181229
Bmp2tm1Jfm/Bmp2tm1Jfm Bmp4tm1Jfm/Bmp4+ Bmp7tm1Jfm/Bmp7+ H2az2Tg(Wnt1-cre)11Rth/H2az2+ involves: 129S4/SvJaeSor * C57BL/6J * CBA/J	absent alisphenoid bone	J:181229
	absent mandibular coronoid process	J:181229
	absent zygomatic bone	J:181229
	cleft palate	J:181229
	small nasal bone	J:181229
Bmp2tm1Jfm/Bmp2tm1Jfm Bmp4tm1Jfm/Bmp4+ Bmp7tm1Jfm/Bmp7tm1Jfm H2az2Tg(Wnt1-cre)11Rth/H2az2+ involves: 129S4/SvJaeSor * C57BL/6J * CBA/J	abnormal temporal bone squamous part morphology	J:181229
	abnormal tympanic ring morphology	J:181229
	absent alisphenoid bone	J:181229
	absent mandibular coronoid process	J:181229
	absent zygomatic bone	J:181229
	cleft palate	J:181229
	small nasal bone	J:181229
Bmp2tm1Jfm/Bmp2tm1Jfm Bmp4tm1Jfm/Bmp4tm1Jfm Bmp7tm1Jfm/Bmp7+ H2az2Tg(Wnt1-cre)11Rth/H2az2+ involves: 129S4/SvJaeSor * C57BL/6J * CBA/J	abnormal interparietal bone morphology	J:181229
	abnormal mandibular angle morphology	J:181229
	abnormal mandibular condyloid process morphology	J:181229
	abnormal nasal bone morphology	J:181229
	absent alisphenoid bone	J:181229
	absent mandibular coronoid process	J:181229
	absent maxilla	J:181229
	absent temporal bone squamous part	J:181229
	absent tympanic ring	J:181229
	absent zygomatic bone	J:181229
	cleft palate	J:181229
Bmp2tm1Jfm/Bmp2tm1Jfm Bmp4tm1Jfm/Bmp4tm1Jfm Bmp7tm1Jfm/Bmp7tm1Jfm H2az2Tg(Wnt1-cre)11Rth/H2az2+ involves: 129S4/SvJaeSor * C57BL/6J * CBA/J	abnormal craniofacial bone morphology	J:181229
	abnormal interparietal bone morphology	J:181229
	abnormal mandible morphology	J:181229
	abnormal nasal bone morphology	J:181229
	absent alisphenoid bone	J:181229
	absent mandibular angle	J:181229
	absent mandibular condyloid process	J:181229
	absent mandibular coronoid process	J:181229
	absent maxilla	J:181229
	absent temporal bone squamous part	J:181229
	absent tympanic ring	J:181229
	absent zygomatic bone	J:181229
	cleft palate	J:181229
	large anterior fontanelle	J:181229
Bmp4tm1Blh/Bmp4+ Bmp7tm1Kry/Bmp7+ involves: 129S2/SvPas * 129S7/SvEvBrd	abnormal digit morphology	J:48538
	abnormal sternum morphology	J:48538
	abnormal thoracic cage morphology	J:48538
	asymmetric rib joints	J:48538
	normal growth/size/body region phenotype	J:48538
	polydactyly	J:48538
	rib fusion	J:48538
	split xiphoid process	J:48538
Bmp4tm1Jfm/Bmp4tm1Jfm Bmp7tm1Jfm/Bmp7tm1Jfm H2az2Tg(Wnt1-cre)11Rth/H2az2+ involves: 129S4/SvJaeSor * C57BL/6J * CBA/J	abnormal mandible morphology	J:181229
	cleft palate	J:181229
	decreased tympanic ring size	J:181229
	large anterior fontanelle	J:181229
	small temporal bone squamous part	J:181229
Bmp4tm4Blh/Bmp4+ Bmp7tm1.1Dgra/Bmp7tm1.1Dgra Hoxa3tm1(cre)Moon/Hoxa3+ involves: 129S6/SvEvTac * C57BL/6NTac	absent urinary bladder	J:192045
	anal stenosis	J:192045
	sirenomelia	J:192045
Bmp7Tg(BCL2)114Cro/Bmp7Tg(BCL2)114Cro involves: C3H/HeJ * C57BL/6	abnormal distal convoluted tubule morphology	J:38288
	abnormal kidney development	J:38288
	abnormal retina pigment epithelium morphology	J:38288
	abnormal retina pigmentation	J:38288
	abnormal sacral vertebrae morphology	J:38288
	abnormal skeleton morphology	J:38288
	abnormal vertebrae morphology	J:38288
	aphakia	J:38288
	basisphenoid bone foramen	J:38288
	decreased birth weight	J:38288
	decreased bone mineral density	J:38288
	decreased lumbar vertebrae number	J:38288
	decreased nephron number	J:38288
	delayed bone ossification	J:38288
	eyelids fail to open	J:38288
	fusion of vertebral bodies	J:38288
	impaired coordination	J:38288
	kinked tail	J:38288
	neonatal lethality, incomplete penetrance	J:38288
	polycystic kidney	J:38288
	polydactyly	J:38288
	premature death	J:38288
	rib fusion	J:38288
	small kidney	J:38288
	tremors	J:38288
	xiphoid process foramen	J:38288
Bmp7tm1Kry/Bmp7tm1Kry Nogtm1Amc/Nogtm1Amc either: (involves: 129S1/Sv * C57BL/6) or (involves: 129S1/Sv * CD-1 * ICR)	normal digestive/alimentary phenotype	J:118341
	normal nervous system phenotype	J:118341
	prenatal lethality, complete penetrance	J:118341
Bmp7tm1Rob/Bmp7+ Bmp8atm1Blh/Bmp8atm1Blh involves: 129S/SvEv * 129S6/SvEvTac * Black Swiss	abnormal epididymis morphology	J:78867
	decreased testis weight	J:78867
Bmp7tm1Rob/Bmp7+ Bmp8atm1Blh/Bmp8atm1Blh involves: 129S/SvEv * 129S6/SvEvTac * Black Swiss * C57BL/6	abnormal epididymis morphology	J:78867
	abnormal male germ cell morphology	J:78867
	abnormal spermatogenesis	J:78867
	epididymis degeneration	J:78867
	epididymis epithelium degeneration	J:78867
	granulomatous inflammation	J:78867
	male infertility	J:78867
Bmp7tm1Rob/Bmp7+ Fbn2tm1Rmz/Fbn2+ either: (involves: 129/Sv * 129S/SvEv) or (involves: 129/Sv * 129S/SvEv * C57BL/6J)	polysyndactyly	J:70592
Bmp7tm1Rob/Bmp7tm1Rob Bmpr1btm1Kml/Bmpr1btm1Kml involves: 129S/SvEv * C57BL/6J	abnormal humerus morphology	J:59282
	abnormal scapula morphology	J:59282
	brachyphalangia	J:59282
	decreased autopod size	J:59282
	short humerus	J:59282
	short metacarpal bones	J:59282
	short radius	J:59282
	short ulna	J:59282
Bmp7tm6(cre)Rob/Bmp7+ Smad4tm1Rob/Smad4tm1.1Rob involves: 129S/SvEv * C57BL/6 * SJL	abnormal kidney development	J:108109
	abnormal renal glomerulus morphology	J:108109
	decreased kidney collecting duct number	J:108109
	hydroureter	J:108109
	kidney cyst	J:108109
	perinatal lethality, incomplete penetrance	J:108109
	postnatal lethality, complete penetrance	J:108109
	small kidney	J:108109