101 phenotypes from 8 alleles in 10 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Msx2m1Btlr/Msx2m1Btlr C57BL/6J-Msx2m1Btlr	abnormal hair shedding	J:204501
	alopecia	J:204501
	delayed hair regrowth	J:204501
	microphthalmia	J:204501
Msx2tm1.1Yvla/Msx2tm1.1Yvla involves: 129S2/SvPas * BALB/c * C57BL/6 * SJL	abnormal cerebellum development	J:136241
	abnormal skeleton development	J:136241
	alopecia	J:136241
	embryonic growth retardation	J:136241
Msx2tm1Rem/Msx2tm1Rem Tg(Msx2-cre)5Rem/0 involves: 129S6/SvEvTac * C57BL/6 * SJL	abnormal neurocranium morphology	J:128624
	alopecia	J:128624
Msx2tm1Rilm/Msx2+ involves: 129S4/SvJae * BALB/c * C57BL/6	frontal bone foramen	J:87044
Msx2tm1Rilm/Msx2tm1Rilm either: (involves: 129S4/SvJae) or (involves: 129S4/SvJae * BALB/c) or (involves: 129S4/SvJae * C57BL/6J)	abnormal appendicular skeleton morphology	J:61509
	abnormal axial skeleton morphology	J:61509
	abnormal bone ossification	J:61509
	abnormal cerebellum anterior vermis morphology	J:61509
	abnormal cerebellum development	J:61509
	abnormal enamel organ morphology	J:61509
	abnormal long bone hypertrophic chondrocyte zone	J:61509
	abnormal mammary gland embryonic development	J:61509
	abnormal neurocranium morphology	J:61509
	abnormal stellate reticulum morphology	J:61509
	abnormal stratum intermedium morphology	J:61509
	abnormal trabecular bone morphology	J:61509
	absent cerebellum vermis lobule IX	J:61509
	absent cerebellum vermis lobule VIII	J:61509
	alopecia	J:61509
	ameloblast degeneration	J:61509
	normal behavior/neurological phenotype	J:61509
	big ears	J:61509
	brittle teeth	J:61509
	cerebellum vermis hypoplasia	J:61509
	chondrodystrophy	J:61509
	curly vibrissae	J:73670
	decreased bone mineral density	J:61509
	decreased chondrocyte number	J:61509
	decreased compact bone thickness	J:61509
	decreased osteoclast cell number	J:61509
	degenerate molars	J:61509
	delaminated cerebellar granule layer	J:61509
	delaminated Purkinje cell layer	J:61509
	frontal bone foramen	J:61509
	normal integument phenotype	J:73670
	long nails	J:61509
	malocclusion	J:61509
	normal mortality/aging	J:61509
	normal nervous system phenotype	J:61509
	premature hair loss	J:61509
	short femur	J:61509
	short tibia	J:61509
	short vibrissae	J:73670
	small interparietal bone	J:61509
	small supraoccipital bone	J:61509
	tonic seizures	J:61509
Msx2tm1Rilm/Msx2tm1Rilm involves: 129S4/SvJae	abnormal cornea morphology	J:184697
	abnormal eye development	J:184697
	abnormal eye morphology	J:184697
	abnormal lens morphology	J:184697
	abnormal lens vesicle development	J:184697
	abnormal optic vesicle formation	J:184697
	abnormal retina pigment epithelium morphology	J:184697
	anterior iris synechia	J:184697
	cornea opacity	J:184697
	decreased cornea epithelium thickness	J:184697
	increased cornea stroma thickness	J:184697
	increased cornea thickness	J:184697
	iris hyperplasia	J:184697
	microphthalmia	J:184697
	narrow eye opening	J:184697
	retina fold	J:184697
	small lens	J:184697
	vitreous body deposition	J:184697
Msx2tm1Rilm/Msx2tm1Rilm involves: 129S4/SvJae * BALB/c * C57BL/6	abnormal frontal bone morphology	J:87044
Msx2tm1Rilm/Msx2tm1Rilm involves: 129S4/SvJae * BALB/c * CD-1	normal cardiovascular system phenotype	J:139946
Msx2tm1Rilm/Msx2tm1Rilm involves: 129S4/SvJae * CD-1	abnormal nail matrix morphology	J:173664
	abnormal nail morphology	J:173664
	deformed nails	J:173664
	long toenails	J:173664
Msx2tm1Yvla/Msx2tm1Yvla involves: 129S2/SvPas * C57BL/6 * SJL	no abnormal phenotype detected	J:136241
Tg(CMV-Msx2*P7H)1Rem/0 involves: C57BL/6 * CBA/J	ectopic cranial bone	J:26513
	premature cranial suture closure	J:26513
Tg(Msx2)1Rem/0 involves: C57BL/6 * CBA/J	abnormal coat/ hair morphology	J:56777
	abnormal dermal layer morphology	J:56777
	abnormal ear morphology	J:26513
	abnormal epidermal layer morphology	J:56777
	abnormal epidermis stratum basale morphology	J:56777
	abnormal eye morphology	J:26513
	abnormal hair follicle bulb morphology	J:56777
	abnormal hair follicle inner root sheath morphology	J:56777
	abnormal hair follicle matrix region morphology	J:56777
	abnormal hair follicle morphology	J:56777
	abnormal hair follicle orientation	J:56777
	abnormal hair shaft morphology	J:56777
	abnormal skin morphology	J:56777
	dermis papillary layer hypercellularity	J:56777
	disorganized inner root sheath cells	J:56777
	disorganized matrix sheath cells	J:56777
	disorganized outer root sheath cells	J:56777
	disorganized suprabasal layer	J:56777
	distorted hair follicle pattern	J:56777
	ectopic cranial bone	J:26513
	epidermal desquamation	J:56777
	flaky skin	J:56777
	focal hair loss	J:56777
	hyperkeratosis	J:56777
	premature cranial suture closure	J:26513
	scaly skin	J:56777
	short hair	J:56777
	thick epidermis	J:56777
	thick epidermis suprabasal layer	J:56777
	thick skin	J:56777
	thin hair follicle outer root sheath	J:56777
Tg(Timp1-Msx2*P7H)1Rem/0 involves: C57BL/6 * CBA/J	premature cranial suture closure	J:26513