60 phenotypes from multigenic genotypes

Allelic Composition Genetic Background	Annotated Term	Reference
Baxtm1Sjk/Baxtm1Sjk Bmpr1atm1Bhr/Bmpr1atm2.1Bhr Tg(Sftpc-cre)1Blh/0 involves: 129 * C57BL/6 * DBA/2 * ICR	abnormal lung development	J:106392
Bmpr1atm1Bhr/Bmpr1a+ Col2a1tm1.1Ksec/Col2a1+ involves: 129S7/SvEvBrd * 129X1/SvJ * C57BL/6	abnormal neural tube morphology	J:163739
	abnormal tail morphology	J:163739
	enophthalmos	J:163739
Bmpr1atm1Bhr/Bmpr1a+ Col2a1tm1.1Ksec/Col2a1tm1.1Ksec involves: 129S7/SvEvBrd * 129X1/SvJ * C57BL/6	cyclopia	J:163739
	microcephaly	J:163739
	midface hypoplasia	J:163739
	prenatal lethality, incomplete penetrance	J:163739
Bmpr1atm1Bhr/Bmpr1atm2.1Bhr Bmpr1btm1Kml/Bmpr1b+ Tg(Six3-cre)69Frty/0 involves: 129S/SvEv	abnormal retina ganglion cell morphology	J:96964
Bmpr1atm1Bhr/Bmpr1atm2.1Bhr Bmpr1btm1Kml/Bmpr1btm1Kml Tg(Six3-cre)69Frty/0 involves: 129S/SvEv	abnormal eye development	J:96964
	abnormal retina morphology	J:96964
	abnormal retina pigment epithelium morphology	J:96964
	anophthalmia	J:96964
	increased retina apoptosis	J:96964
Bmpr1atm2.1Bhr/Bmpr1atm2.1Bhr Bmpr1btm1Kml/Bmpr1btm1Kml Tg(Col2a1-cre)1Bhr/? involves: 129S/SvEv * 129S7/SvEvBrd * C57BL/6 * SJL	abnormal cartilage development	J:97410
	abnormal chondrocyte differentiation	J:97410
	abnormal chondrocyte morphology	J:97410
	abnormal digit development	J:97410
	abnormal epiphyseal plate morphology	J:97410
	abnormal notochord morphology	J:97410
	abnormal skeleton development	J:97410
	abnormal ulna morphology	J:97410
	abnormal vertebrae development	J:97410
	abnormal vertebral column morphology	J:97410
	chondrodystrophy	J:97410
	decreased fetal size	J:97410
	decreased radius size	J:97410
	failure of endochondral bone ossification	J:97410
	lethality throughout fetal growth and development, complete penetrance	J:97410
	short limbs	J:97410
	short snout	J:97410
	short tail	J:97410
Bmpr1atm2.1Bhr/Bmpr1atm2.1Bhr Ctnnb1tm1Mmt/Ctnnb1+ Krt14tm1.1(cre)Wbm/Krt14+ involves: 129P2/OlaHsd * 129S7/SvEvBrd * 129X1/SvJ	decreased tumor-free survival time	J:199091
	increased hair follicle number	J:199091
	increased salivary gland tumor incidence	J:199091
	increased squamous cell carcinoma incidence	J:199091
Gt(ROSA)26Sortm1(CAG-Bmpr1a)Que/Gt(ROSA)26Sor+ Shhtm1(EGFP/cre)Cjt/? Not Specified	abnormal esophageal epithelium morphology	J:166768
	abnormal forestomach morphology	J:166768
	preweaning lethality, complete penetrance	J:166768
Tg(CAG-Bmpr1a*,-lacZ)1Nobs/Tg(CAG-Bmpr1a*,-lacZ)1Nobs B6.Cg-Tg(CAG-Bmpr1a*,-lacZ)1Nobs	no abnormal phenotype detected	J:192670
Tg(CAG-Bmpr1a*,-lacZ)1Nobs/0 Tg(Mpz-cre)94Imeg/0 involves: 129X1/SvJ * C57BL/6J	abnormal bone ossification	J:192670
	abnormal craniofacial development	J:192670
	abnormal facial morphology	J:192670
	abnormal frontonasal mesenchyme morphology	J:192670
	abnormal head mesenchyme morphology	J:192670
	abnormal nasal bone morphology	J:192670
	abnormal nasal septum morphology	J:192670
	abnormal neurocranium morphology	J:192670
	abnormal suckling behavior	J:192670
	belly spot	J:192670
	cleft palate	J:192670
	decreased survivor rate	J:192670
	facial cleft	J:192670
	large anterior fontanelle	J:192670
	midline facial cleft	J:192670
	neonatal lethality, incomplete penetrance	J:192670
	ocular hypertelorism	J:192670
	short face	J:192670
	small frontal bone	J:192670
	ventricular septal defect	J:192670