56 phenotypes from 4 alleles in 6 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Ldb1tm1.1Gsv/Ldb1tm1.1Gsv involves: 129P2/OlaHsd * C57BL/6 * FVB	abnormal embryonic erythropoiesis	J:196469
	abnormal vascular development	J:196469
	abnormal visceral yolk sac morphology	J:196469
Ldb1tm1Lmgd/Ldb1+ involves: C3H/He * C57BL/6	no abnormal phenotype detected	J:98485
Ldb1tm1Lmgd/Ldb1tm1Lmgd involves: CD-1	abnormal allantois morphology	J:81152
	abnormal craniofacial morphology	J:81152
	abnormal extraembryonic tissue morphology	J:81152
	abnormal foregut morphology	J:81152
	abnormal heart morphology	J:81152
	abnormal hematopoietic system morphology/development	J:81152
	abnormal neural plate morphology	J:81152
	abnormal primitive streak formation	J:81152
	abnormal primitive streak morphology	J:81152
	abnormal primordial germ cell morphology	J:81152
	abnormal rhombomere 3 morphology	J:81152
	abnormal rhombomere 5 morphology	J:81152
	abnormal visceral yolk sac morphology	J:81152
	absent allantois	J:81152
	absent heart	J:81152
	absent midbrain-hindbrain boundary	J:81152
	absent visceral yolk sac blood islands	J:81152
	decreased embryo size	J:81152
	embryonic growth arrest	J:81152
	embryonic lethality, complete penetrance	J:81152
	embryonic-extraembryonic boundary constriction	J:81152
	failure of chorioallantoic fusion	J:81152
	fused somites	J:81152
	increased somite number	J:81152
	kinked neural tube	J:81152
	rostral body truncation	J:81152
	rostral-caudal axis duplication	J:81152
	split notochord	J:81152
Ldb1tm1Lmgd/Ldb1tm2Lmgd H2az2Tg(Wnt1-cre)11Rth/H2az2+ involves: C57BL/6J * CBA/J	abnormal diastema morphology	J:208345
	abnormal palatal mesenchymal cell proliferation	J:208345
	abnormal palatal shelf elevation	J:208345
	abnormal palatal shelf morphology	J:208345
	abnormal tongue position	J:208345
	arrest of tooth development	J:208345
	cleft secondary palate	J:208345
	normal craniofacial phenotype	J:208345
	decreased molar number	J:208345
	decreased palatal shelf size	J:208345
	neonatal lethality, complete penetrance	J:208345
Ldb1tm1Witz/Ldb1tm1Witz Tg(NPHS2-cre)295Lbh/0 involves: C57BL/6 * SJL	abnormal glomerular capillary endothelium morphology	J:122505
	abnormal podocyte foot process morphology	J:122505
	abnormal renal glomerulus basement membrane morphology	J:122505
	absent glomerular endothelium fenestra	J:122505
	albuminuria	J:122505
	dilated renal tubule	J:122505
	podocyte foot process effacement	J:122505
	premature death	J:122505
	renal cast	J:122505
	renal glomerular synechia	J:122505
	renal glomerulus atrophy	J:122505
Ldb1tm2Lmgd/Ldb1tm2Lmgd Tg(Nes-cre)1Kln/0 involves: C57BL/6 * FVB/N * SJL	absent cerebellar foliation	J:123471
	decreased Purkinje cell number	J:123471
	small cerebellum	J:123471