81 phenotypes from 7 alleles in 7 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Nabp2tm1.1Kkha/Nabp2tm1.1Kkha Cd19tm1(cre)Cgn/Cd19+ involves: 129P2/OlaHsd * C57BL/6	normal immune system phenotype	J:195140
Nabp2tm1.1Kkha/Nabp2tm1.1Kkha Gt(ROSA)26Sortm9(cre/ESR1)Arte/Gt(ROSA)26Sor+ involves: C57BL/6 * C57BL/6NTac	abnormal male germ cell apoptosis	J:195140
	abnormal male germ cell morphology	J:195140
	abnormal small intestine morphology	J:195140
	chromosomal instability	J:195140
	decreased body length	J:195140
	decreased litter size	J:195140
	decreased testis weight	J:195140
	normal hematopoietic system phenotype	J:195140
	increased B cell derived lymphoma incidence	J:195140
	increased cellular sensitivity to ionizing radiation	J:195140
	increased hepatocellular carcinoma incidence	J:195140
	increased leukemia incidence	J:195140
	increased mortality induced by ionizing radiation	J:195140
	increased T cell derived lymphoma incidence	J:195140
	increased thymocyte apoptosis	J:195140
	increased tumor incidence	J:195140
	oligozoospermia	J:195140
	reduced male fertility	J:195140
	normal reproductive system phenotype	J:195140
	small testis	J:195140
	testis degeneration	J:195140
Nabp2tm1.1Nfel/Nabp2tm1.2Nfel Cd19tm1(cre)Cgn/Cd19+ involves: 129P2/OlaHsd * C57BL/6 * FVB/N * SJL	normal immune system phenotype	J:190019
Nabp2tm1.1Schg/Nabp2tm1.1Schg involves: 129S7/SvEvBrd * C57BL/6	abnormal hindlimb morphology	J:228558
	abnormal telomere morphology	J:228558
	chromosomal instability	J:228558
	decreased birth body size	J:228558
	neonatal lethality, complete penetrance	J:228558
Nabp2tm1.2Kkha/Nabp2tm1.2Kkha involves: BALB/cJ * C57BL/6J	abnormal autopod morphology	J:195140
	abnormal bone mineralization	J:195140
	abnormal bone ossification	J:195140
	abnormal craniofacial morphology	J:195140
	abnormal forelimb morphology	J:195140
	abnormal hindlimb morphology	J:195140
	abnormal limb development	J:195140
	abnormal lung development	J:195140
	abnormal mandible morphology	J:195140
	abnormal premaxilla morphology	J:195140
	abnormal pulmonary alveolus morphology	J:195140
	abnormal pulmonary alveolus wall morphology	J:195140
	abnormal rib joint morphology	J:195140
	abnormal rib morphology	J:195140
	abnormal snout morphology	J:195140
	abnormal sternocostal joint morphology	J:195140
	abnormal thoracic cage morphology	J:195140
	abnormal thoracic cage shape	J:195140
	abnormal tympanic ring morphology	J:195140
	abnormal type II pneumocyte morphology	J:195140
	absent fibula	J:195140
	normal cellular phenotype	J:195140
	cleft palate	J:195140
	decreased birth body size	J:195140
	decreased fetal weight	J:195140
	decreased length of long bones	J:195140
	hindlimb oligodactyly	J:195140
	micrognathia	J:195140
	neonatal lethality, complete penetrance	J:195140
	primary atelectasis	J:195140
	respiratory distress	J:195140
	short femur	J:195140
	short humerus	J:195140
	short radius	J:195140
	short scapula	J:195140
	short tibia	J:195140
	short ulna	J:195140
	small thoracic cage	J:195140
Nabp2tm1.2Nfel/Nabp2tm1.2Nfel involves: C57BL/6 * FVB/N * SJL	abnormal bone structure	J:190019
	abnormal cartilage development	J:190019
	abnormal cranium morphology	J:190019
	abnormal deltoid tuberosity morphology	J:190019
	abnormal limb development	J:190019
	abnormal rib development	J:190019
	abnormal scapular spine morphology	J:190019
	abnormal skeleton morphology	J:190019
	abnormal tympanic ring morphology	J:190019
	absent deltoid tuberosity	J:190019
	chromosomal instability	J:190019
	cleft palate	J:190019
	decreased bone volume	J:190019
	fetal growth retardation	J:190019
	hindlimb oligodactyly	J:190019
	increased embryonic tissue cell apoptosis	J:190019
	mandible hypoplasia	J:190019
	perinatal lethality, complete penetrance	J:190019
	small thoracic cage	J:190019
Nabp2tm1b(KOMP)Wtsi/Nabp2tm1b(KOMP)Wtsi C57BL/6N-Nabp2tm1b(KOMP)Wtsi/Ucd	abnormal craniofacial morphology	J:211773
	abnormal embryo size	J:211773
	abnormal limb morphology	J:211773
	edema	J:211773
	preweaning lethality, complete penetrance	J:211773
Nabp2tm1Schg/Nabp2tm1Schg involves: 129S7/SvEvBrd * C57BL/6	chromosomal instability	J:228558
	increased mortality induced by gamma-irradiation	J:228558
	increased spleen red pulp amount	J:228558
	premature death	J:228558