70 phenotypes from 11 alleles in 12 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Cd19tm1(cre)Cgn/Cd19+ Prdm1tm1Clme/Prdm1tm1Clme involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ	abnormal B cell differentiation	J:101890
	abnormal memory B cell number	J:101890
	abnormal plasma cell differentiation	J:101890
	abnormal plasma cell morphology	J:101890, J:114881
	decreased IgG level	J:101890
	decreased IgM level	J:101890
	decreased immunoglobulin level	J:101890
	decreased plasma cell number	J:101890
	increased spleen germinal center number	J:101890
	increased spleen germinal center size	J:101890
Prdm1b2b1765Clo/Prdm1b2b1765Clo C57BL/6J-Prdm1b2b1765Clo	abnormal aortic valve morphology	J:175213
	abnormal left subclavian artery morphology	J:175213
	atrioventricular septal defect	J:175213
	double outlet right ventricle	J:175213
	right aortic arch	J:175213
	vascular ring	J:175213
Prdm1em1(IMPC)Bay/Prdm1+ C57BL/6N-Prdm1em1(IMPC)Bay/BayMmucd	abnormal embryo size	J:211773
Prdm1em1(IMPC)Bay/Prdm1em1(IMPC)Bay C57BL/6N-Prdm1em1(IMPC)Bay/BayMmucd	abnormal heart morphology	J:211773
	embryonic lethality prior to tooth bud stage	J:211773
	preweaning lethality, complete penetrance	J:211773
Prdm1tm1.1Clme/Prdm1+ involves: 129S1/Sv * 129X1/SvJ * FVB/N * ICR	decreased primordial germ cell number	J:101718
Prdm1tm1.1Clme/Prdm1tm1.1Clme involves: 129S1/Sv * 129X1/SvJ * FVB/N * ICR	abnormal dermomyotome development	J:101718
	abnormal dorsal aorta morphology	J:101718
	abnormal pharyngeal arch mesenchyme morphology	J:101718
	abnormal pharyngeal arch morphology	J:101718
	abnormal placenta labyrinth morphology	J:101718
	absent second pharyngeal arch	J:101718
	absent third pharyngeal arch	J:101718
	decreased embryo size	J:101718
	decreased primordial germ cell number	J:101718
	embryonic lethality during organogenesis, complete penetrance	J:101718
	hemorrhage	J:101718
Prdm1tm1.1Clme/Prdm1tm1.1Liz involves: 129S/SvEv * 129S1/Sv * 129X1/SvJ	abnormal germ cell morphology	J:153979
	absent oocytes	J:153979
	azoospermia	J:153979
	decreased primordial germ cell number	J:153979
	decreased testis weight	J:153979
	forelimb oligodactyly	J:153979
	lethality throughout fetal growth and development, incomplete penetrance	J:153979
	postnatal lethality, incomplete penetrance	J:153979
Prdm1tm1.1Clme/Prdm1tm2.1Liz involves: 129S/SvEv * 129S1/Sv * 129X1/SvJ	no abnormal phenotype detected	J:153979
Prdm1tm1.1Clme/Prdm1tm2Rob involves: 129S/Sv * 129X1/Sv * C57BL/6 * FVB/N * ICR	abnormal dermomyotome development	J:101718
	abnormal dorsal aorta morphology	J:101718
	abnormal pharyngeal arch mesenchyme morphology	J:101718
	abnormal pharyngeal arch morphology	J:101718
	abnormal placenta labyrinth morphology	J:101718
	absent primordial germ cells	J:101718
	absent second pharyngeal arch	J:101718
	absent third pharyngeal arch	J:101718
	decreased embryo size	J:101718
	embryonic lethality during organogenesis, complete penetrance	J:101718
	hemorrhage	J:101718
Prdm1tm1.1Liz/Prdm1tm1.1Liz involves: 129S/SvEv	abnormal splenocyte physiology	J:163979
	absent plasma cells	J:196531
Prdm1tm1Clme/Prdm1tm1Clme Tg(Itgax-cre)1-1Reiz/0 involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA	abnormal CD4-positive, alpha-beta T cell physiology	J:178876
	abnormal germinal center B cell physiology	J:178876
	abnormal immune system physiology	J:178876
	abnormal kidney morphology	J:178876
	abnormal mesangial cell morphology	J:178876
	abnormal T follicular helper cell differentiation	J:178876
	increased anti-double stranded DNA antibody level	J:178876
	increased anti-nuclear antigen antibody level	J:178876
	increased autoantibody level	J:178876
	increased germinal center B cell number	J:178876
	increased IgG level	J:178876
	increased immunoglobulin level	J:178876
	increased interleukin-6 secretion	J:178876
	increased spleen germinal center number	J:178876
	increased splenocyte number	J:178876
	increased T follicular helper cell number	J:178876
	increased urine protein level	J:178876
	kidney inflammation	J:178876
Prdm1tm1Clme/Prdm1tm1Clme Tg(Pdx1-cre)6Tuv/0 involves: 129S1/Sv * 129X1/SvJ * FVB/N	normal endocrine/exocrine gland phenotype	J:245611
Prdm1tm1Masu/Prdm1+ involves: 129P2/OlaHsd * C57BL/6 * CBA	decreased primordial germ cell number	J:99994
Prdm1tm1Masu/Prdm1tm1Masu involves: 129P2/OlaHsd * C57BL/6 * CBA	abnormal primordial germ cell migration	J:99994
	decreased primordial germ cell number	J:99994
Prdm1tm1Nutt/Prdm1tm1Nutt involves: C57BL/6	prenatal lethality, complete penetrance	J:93944
Prdm1tm1Rob/Prdm1+ involves: 129S/SvEv * C57BL/6	decreased primordial germ cell number	J:101718
Prdm1tm1Rob/Prdm1tm1Rob involves: 129S/SvEv * C57BL/6	abnormal dorsal aorta morphology	J:101718
	abnormal myotome development	J:101718
	abnormal pharyngeal arch mesenchyme morphology	J:101718
	abnormal pharyngeal arch morphology	J:101718
	abnormal placenta labyrinth morphology	J:101718
	abnormal third pharyngeal arch morphology	J:101718
	absent second pharyngeal arch	J:101718
	decreased embryo size	J:101718
	decreased primordial germ cell number	J:101718
	embryonic lethality during organogenesis, complete penetrance	J:101718
	hemorrhage	J:101718
Prdm1tm2.1Liz/Prdm1tm2.1Liz involves: 129S/SvEv	normal immune system phenotype	J:153979
	no abnormal phenotype detected	J:153979
Prdm1tm2.1Nutt/Prdm1tm2.1Nutt Tg(Lck-cre)1Cwi/? involves: C57BL/6	increased susceptibility to Orthomyxoviridae infection	J:151858
Prdm1tm2Rob/Prdm1+ involves: 129S/SvEv * C57BL/6	decreased primordial germ cell number	J:101718
Prdm1tm2Rob/Prdm1tm2Rob involves: 129S/SvEv	abnormal placenta development	J:187742
	abnormal spongiotrophoblast layer morphology	J:187742
	decreased trophoblast giant cell number	J:187742
	uterine hemorrhage	J:187742
Prdm1tm2Rob/Prdm1tm2Rob involves: 129S/SvEv * C57BL/6	abnormal dorsal aorta morphology	J:101718
	abnormal myotome development	J:101718
	abnormal pharyngeal arch mesenchyme morphology	J:101718
	abnormal pharyngeal arch morphology	J:101718
	abnormal placenta labyrinth morphology	J:101718
	abnormal third pharyngeal arch morphology	J:101718
	absent second pharyngeal arch	J:101718
	decreased embryo size	J:101718
	decreased primordial germ cell number	J:101718
	embryonic lethality during organogenesis, complete penetrance	J:101718
	hemorrhage	J:101718