58 phenotypes from 2 alleles in 3 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Nkx2-3tm1Hha/Nkx2-3tm1Hha involves: 129S4/SvJae	abnormal leukocyte migration	J:62129
	abnormal marginal zone B cell morphology	J:62129
	abnormal mesenteric lymph node morphology	J:62129
	abnormal metallophilic macrophage morphology	J:62129
	abnormal Peyer's patch follicle morphology	J:62129
	abnormal spleen marginal sinus morphology	J:62129
	abnormal spleen marginal zone macrophage morphology	J:62129
	abnormal spleen morphology	J:62129
	abnormal spleen periarteriolar lymphoid sheath morphology	J:62129
	absent marginal zone B cells	J:62129
	absent spleen marginal zone	J:62129
	decreased B cell number	J:62129
	decreased lymphocyte cell number	J:62129
	decreased Peyer's patch number	J:62129
	decreased spleen weight	J:62129
	decreased spleen white pulp amount	J:62129
	decreased T cell number	J:62129
	intermingled spleen red and white pulp	J:62129
	small Peyer's patches	J:62129
	small spleen	J:62129
Nkx2-3tm1Hha/Nkx2-3tm1Hha involves: 129S4/SvJae * C57BL/6	abnormal blood vessel morphology	J:54198
	abnormal cell proliferation	J:54198
	abnormal crypts of Lieberkuhn morphology	J:54198
	abnormal ileum morphology	J:54198
	abnormal intestinal epithelium morphology	J:54198
	abnormal intestine morphology	J:54198
	abnormal jejunum morphology	J:54198
	abnormal small intestine morphology	J:54198
	abnormal spleen primary B follicle morphology	J:54198
	abnormal splenic cell ratio	J:54198
	absent spleen	J:54198
	absent spleen marginal zone	J:54198
	cachexia	J:54198
	decreased spleen white pulp amount	J:54198
	postnatal growth retardation	J:54198
	postnatal lethality, incomplete penetrance	J:54198
	small spleen	J:54198
Nkx2-3tm1Rph/Nkx2-3tm1Rph involves: 129S1/Sv * C57BL/6	abnormal duodenum morphology	J:64018
	abnormal gut-associated lymphoid tissue morphology	J:64018
	abnormal intestinal mucosa morphology	J:64018
	abnormal intestinal peristalsis	J:64018
	abnormal intestine morphology	J:64018
	abnormal jejunum crypts of Lieberkuhn morphology	J:64018
	abnormal jejunum morphology	J:64018
	abnormal leukocyte migration	J:64018
	abnormal mesenteric lymph node morphology	J:64018
	abnormal metallophilic macrophage morphology	J:64018
	abnormal molar cusp morphology	J:80726
	abnormal oropharynx morphology	J:80726
	abnormal small intestinal villus morphology	J:64018
	abnormal small intestine morphology	J:64018
	abnormal spleen B cell follicle morphology	J:64018
	abnormal spleen periarteriolar lymphoid sheath morphology	J:64018
	abnormal spleen red pulp morphology	J:64018
	abnormal sublingual gland morphology	J:80726
	abnormal tooth development	J:80726
	absent spleen	J:64018
	absent spleen marginal zone	J:64018
	decreased CD4-positive, alpha-beta T cell number	J:64018
	decreased circulating triglyceride level	J:64018
	decreased molar number	J:80726
	decreased Peyer's patch number	J:64018
	decreased plasma cell number	J:64018
	delayed intestine development	J:64018
	diarrhea	J:64018
	failure of tooth eruption	J:80726
	increased enterocyte cell number	J:64018
	increased leukocyte cell number	J:64018
	postnatal lethality, incomplete penetrance	J:64018
	small cecum	J:64018
	small Peyer's patches	J:64018
	small spleen	J:64018
	spleen atrophy	J:64018
	steatorrhea	J:64018