94 phenotypes from 6 alleles in 9 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Tg(Sox10-cre)1Wdr/0 Twsg1tm1Aptr/Twsg1tm1Aptr involves: C57BL/6 * CBA	abnormal frontonasal prominence morphology	J:173627
	abnormal telencephalon development	J:173627
	fused first pharyngeal arch	J:173627
	small first pharyngeal arch	J:173627
Twsg1tm1.1Mboc/Twsg1tm1.1Mboc 129S/SvEv-Twsg1tm1.1Mboc	abnormal craniofacial morphology	J:88784
	abnormal jaw morphology	J:88784
	abnormal vertebral arch morphology	J:88784
	decreased body size	J:88784
	decreased body weight	J:88784
	lethality at weaning, incomplete penetrance	J:88784
	neonatal lethality, incomplete penetrance	J:88784
Twsg1tm1.1Mboc/Twsg1tm1.1Mboc B6.129S7-Twsg1tm1.1Mboc	abnormal cervical vertebrae morphology	J:88784
	abnormal craniofacial development	J:88784
	abnormal craniofacial morphology	J:88784
	abnormal head morphology	J:88784
	abnormal submandibular gland development	J:144153
	absent submandibular gland	J:144153
	agnathia	J:88784
	anophthalmia	J:88784
	cyclopia	J:88784
	decreased mouth size	J:144153
	fused first pharyngeal arch	J:88784
	lowered ear position	J:144153
	microphthalmia	J:88784
	perinatal lethality, incomplete penetrance	J:88784
	postnatal lethality, complete penetrance	J:88784
	single external naris	J:88784
Twsg1tm1.1Mboc/Twsg1tm1.1Mboc involves: 129S7/SvEvBrd * C57BL/6 * FVB/N	abnormal caudal vertebrae morphology	J:88784
	abnormal cervical vertebrae morphology	J:88784
	abnormal foregut morphology	J:88784
	abnormal gait	J:88784
	abnormal oropharynx morphology	J:88784
	abnormal thoracic vertebrae morphology	J:88784
	abnormal vertebrae morphology	J:88784
	abnormal vertebral arch morphology	J:88784
	abnormal vertebral lamina morphology	J:88784
	abnormal vertebral spinous process morphology	J:88784
	alobar holoprosencephaly	J:88784
	decreased body size	J:88784
	decreased body weight	J:88784
	decreased caudal vertebrae number	J:88784
	delayed bone ossification	J:88784
	hindlimb paralysis	J:88784
	kinked tail	J:88784
	premature death	J:88784
	short tail	J:88784
Twsg1tm1Dgen/Twsg1tm1Dgen involves: 129S1/Sv * 129X1/SvJ * C57BL/6	decreased body length	J:101679
	decreased body mass index	J:101679
	decreased body weight	J:101679
	kinked tail	J:101679
	weight loss	J:101679
Twsg1tm1Ecan/Twsg1tm1Ecan involves: 129 * C57BL/6	abnormal skeleton development	J:137597
	abnormal skeleton morphology	J:137597
	abnormal tail morphology	J:137597
	decreased body size	J:137597
	decreased bone mineral content	J:137597
	decreased bone trabecula number	J:137597
	decreased bone volume	J:137597
	decreased circulating osteocalcin level	J:137597
	decreased trabecular bone volume	J:137597
	kinked tail	J:137597
	prenatal lethality, incomplete penetrance	J:137597
	short femur	J:137597
	short tail	J:137597
Twsg1tm1Emdr/Twsg1tm1Emdr involves: 129 * C57BL/6 * SJL	prenatal lethality, incomplete penetrance	J:141243
Twsg1tm1Emdr/Twsg1tm1Emdr involves: 129X1/SvJ * C57BL/6 * SJL	abnormal caudal vertebrae morphology	J:90398
	abnormal intervertebral disk development	J:90398
	abnormal tail morphology	J:90398
	abnormal vertebral arch development	J:90398
	decreased body weight	J:90398
	kinked tail	J:90398
	persistence of notochord tissue	J:90398
	short tail	J:90398
Twsg1tm1Nosa/Twsg1tm1Nosa involves: 129P2/OlaHsd * C57BL/6	abnormal B cell differentiation	J:82738
	abnormal bone marrow cell morphology/development	J:82738
	abnormal gait	J:82738
	abnormal intervertebral disk morphology	J:82738
	abnormal intramembranous bone ossification	J:82738
	abnormal kidney development	J:82738
	abnormal limb bone morphology	J:82738
	abnormal long bone epiphyseal plate morphology	J:82738
	abnormal long bone epiphyseal plate proliferative zone	J:82738
	abnormal skeleton development	J:82738
	abnormal spleen development	J:82738
	abnormal thymus development	J:82738
	abnormal timing of postnatal eyelid opening	J:82738
	cachexia	J:82738
	decreased body size	J:82738
	decreased bone mineral density of femur	J:82738
	decreased bone mineral density of lumbar vertebrae	J:82738
	decreased double-positive T cell number	J:82738
	decreased erythrocyte cell number	J:82738
	decreased immature B cell number	J:82738
	decreased lymphocyte cell number	J:82738
	decreased pre-B cell number	J:82738
	decreased pro-B cell number	J:82738
	decreased spleen white pulp amount	J:82738
	decreased splenocyte number	J:82738
	decreased thymocyte number	J:82738
	decreased width of hypertrophic chondrocyte zone	J:82738
	delayed endochondral bone ossification	J:82738
	disproportionate dwarf	J:82738
	increased granulocyte number	J:82738
	increased monocyte cell number	J:82738
	increased single-positive T cell number	J:82738
	increased thymocyte apoptosis	J:82738
	internal hemorrhage	J:82738
	kinked tail	J:82738
	neonatal lethality, incomplete penetrance	J:82738
	postnatal growth retardation	J:82738
	premature death	J:82738
	pulmonary fibrosis	J:82738
	subarachnoid hemorrhage	J:82738
	thin neurocranium	J:82738
	thrombocytopenia	J:82738
	thymus atrophy	J:82738
	tremors	J:82738