49 phenotypes from 7 alleles in 10 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Id2tm1Ago/Id2tm1Ago B6.129-Id2tm1Ago	abnormal cell differentiation	J:138276
	absent lymph nodes	J:116119
	absent NK cells	J:116119
	normal adipose tissue phenotype	J:138276
	decreased body size	J:138276
	decreased CD8-positive, alpha-beta T cell number	J:116119
	decreased inguinal fat pad weight	J:138276
	decreased interscapular fat pad weight	J:138276
	decreased white adipose tissue amount	J:138276
	postnatal lethality, complete penetrance	J:138276
Id2tm1Gtbz/Id2tm1Gtbz involves: C57BL/6	no abnormal phenotype detected	J:195908
Id2tm1Mais/Id2tm1Mais involves: 129X1/SvJ * C57BL/6	abnormal immune system physiology	J:146624
	abnormal lactation	J:146624
	decreased lean body mass	J:146624
	decreased survivor rate	J:146624
Id2tm1Mais/Id2tm1Mais involves: 129X1/SvJ * C57BL/6 * FVB/N	abnormal circadian behavior phase	J:146624
	arrhythmic circadian behavior persistence	J:146624
	decreased locomotor activity	J:146624
	decreased survivor rate	J:146624
	weight loss	J:146624
Id2tm1Mcha/Id2tm1Mcha involves: C57BL/6 * CD-1	abnormal neuronal precursor proliferation	J:143882
	abnormal olfaction	J:143882
	abnormal olfactory bulb morphology	J:143882
	abnormal rostral migratory stream morphology	J:143882
	loss of dopaminergic neurons	J:143882
	normal nervous system phenotype	J:143882
	premature neuronal precursor differentiation	J:143882
	small olfactory bulb	J:143882
Id2tm1Yyk/Id2tm1Yyk either: (involves: 129S1/Sv * 129X1/SvJ) or (involves: 129S1/Sv * 129X1/SvJ * FVB/NJ)	abnormal common lymphocyte progenitor cell morphology	J:125739
	absent lymph nodes	J:125739
	absent Peyer's patches	J:125739
	decreased NK T cell number	J:125739
Id2tm1Yyk/Id2tm1Yyk involves: 129S1/Sv * 129X1/SvJ	abnormal branching of the mammary ductal tree	J:96305
	abnormal oropharyngeal lymphoid tissue morphology	J:78101
	absent Peyer's patches	J:53267
	decreased body size	J:96305
	decreased lymph node number	J:53267
	decreased NK cell number	J:53267
	distended ileum	J:53267
	distended jejunum	J:53267
	neonatal lethality, incomplete penetrance	J:53267
	postnatal growth retardation	J:53267
Id2tm1Yyk/Id2tm1Yyk involves: 129S1/Sv * 129X1/SvJ * NMRI	abnormal lactation	J:53267, J:65670
	abnormal mammary gland growth during pregnancy	J:65670
	abnormal oropharyngeal lymphoid tissue morphology	J:78101
	abnormal ureteropelvic junction morphology	J:101195
	absent Peyer's patches	J:53267
	normal behavior/neurological phenotype	J:65670
	decreased lymph node number	J:53267
	decreased NK cell number	J:53267
	distended ileum	J:53267
	distended jejunum	J:53267
	hydronephrosis	J:101195
	ischuria	J:101195
	postnatal growth retardation	J:53267
	small inner medullary pyramid	J:101195
	ureteropelvic junction stenosis	J:101195
Id2tm2.1Gtbz/Id2tm2.1Gtbz Tg(Itgax-cre)1-1Reiz/0 involves: C57BL/6 * CBA	normal hematopoietic system phenotype	J:194760
	normal immune system phenotype	J:194760
Id2tm2b(EUCOMM)Wtsi/Id2+ C57BL/6N-Id2tm2b(EUCOMM)Wtsi/Wtsi	increased blood urea nitrogen level	J:211773
	increased circulating creatinine level	J:211773