34 phenotypes from 6 alleles in 4 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Hoxb2tm1Fmr/Hoxb2tm1Fmr involves: 129	abnormal maternal nurturing	J:54652
	abnormal rhombomere 4 morphology	J:54652
	absent facial nuclei	J:54652
	neonatal lethality, incomplete penetrance	J:54652
	postnatal lethality, incomplete penetrance	J:54652
	premature death	J:54652
	rhombomere transformation	J:54652
Hoxb2tm1Mrc/Hoxb2+ involves: 129S1/Sv * 129X1/SvJ	abnormal arcus anterior morphology	J:37682
	abnormal facial nerve morphology	J:37682
	cervical vertebral transformation	J:37682
	misaligned sternebrae	J:37682
Hoxb2tm1Mrc/Hoxb2tm1Mrc involves: 129S1/Sv * 129X1/SvJ	abnormal arcus anterior morphology	J:37682
	abnormal body wall morphology	J:71389
	abnormal eye physiology	J:37682
	abnormal facial nerve morphology	J:37682
	abnormal lower lip morphology	J:37682
	abnormal maternal nurturing	J:37682
	abnormal sternum morphology	J:37682
	abnormal vertebral arch morphology	J:37682
	absent facial nerve	J:37682
	absent facial nuclei	J:37682
	absent levator nasolabialis muscle	J:37682
	cervical vertebral transformation	J:37682
	decreased body size	J:37682
	facial muscle atrophy	J:37682
	facial paralysis	J:37682
	misaligned sternebrae	J:37682
	narrow face	J:37682
	neonatal lethality, incomplete penetrance	J:37682
	premature death	J:37682
	respiratory distress	J:37682
	small geniculate ganglion	J:37682
	split sternum	J:37682, J:71389
Hoxb2tm2.1Fmr/Hoxb2tm2.1Fmr involves: C57BL/6 * SJL	no abnormal phenotype detected	J:193058
Hoxb2tm2.2Fmr/Hoxb2tm2.2Fmr involves: C57BL/6 * SJL	abnormal brain development	J:193058
	decreased oligodendrocyte progenitor number	J:193058
Hoxb2tm3.1Fmr/Hoxb2+ involves: 129S2/SvPas * C57BL/6	no abnormal phenotype detected	J:197162
Hoxb2tm3.1Fmr/Hoxb2tm3.1Fmr involves: 129S2/SvPas * C57BL/6	no abnormal phenotype detected	J:197162
Hoxb2tm3.2Fmr/Hoxb2tm3.2Fmr involves: 129S2/SvPas * C57BL/6	abnormal brainstem morphology	J:197162
	abnormal cochlear outer hair cell morphology	J:197162
	abnormal cochlear VIII nucleus morphology	J:197162
	abnormal organ of Corti morphology	J:197162
	abnormal pons morphology	J:197162
	increased or absent threshold for auditory brainstem response	J:197162