94 phenotypes from 3 alleles in 6 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
SfnEr/Sfn+ B6CBACa Aw-J/A-SfnEr/J	premature hair loss	J:102931
SfnEr/Sfn+ involves: 129/Sv * C57BL/6	increased skin papilloma incidence	J:12025
	increased squamous cell carcinoma incidence	J:12025
	lethality at weaning, incomplete penetrance	J:6200
	postnatal growth retardation	J:6200
	premature hair loss	J:6200, J:29020
	sparse hair	J:29020
SfnEr/Sfn+ Not Specified	impaired skin barrier function	J:203995
SfnEr/SfnEr B6CBACa Aw-J/A-SfnEr/J	abnormal keratinocyte differentiation	J:102931
	abnormal oral epithelium morphology	J:102931
	absent epidermis stratum corneum	J:102931
	absent epidermis stratum granulosum	J:102931
	epidermal hyperplasia	J:102931
	perinatal lethality, complete penetrance	J:102931
	respiratory distress	J:102931
	shiny skin	J:102931
	short limbs	J:102931
	short tail	J:102931
	thick epidermis	J:102931
SfnEr/SfnEr involves: 129/Sv * C57BL/6	abnormal axial skeleton morphology	J:6200
	abnormal epidermal layer morphology	J:6708
	abnormal epidermis stratum basale morphology	J:6200, J:6708
	abnormal epidermis stratum corneum morphology	J:6708
	abnormal epidermis stratum granulosum morphology	J:6708
	abnormal external auditory canal morphology	J:7243
	abnormal head morphology	J:7243
	abnormal jaw morphology	J:6200, J:7243
	abnormal liver morphology	J:6200
	abnormal mandible morphology	J:7243
	abnormal nasal cavity morphology	J:7243
	abnormal nasopharynx morphology	J:7243
	abnormal oral cavity morphology	J:6200
	abnormal perineum morphology	J:6200
	abnormal phalanx morphology	J:6200
	abnormal pharynx morphology	J:7243
	abnormal radius morphology	J:6200
	abnormal spine curvature	J:7243
	abnormal tongue morphology	J:6200, J:7243
	anal atresia	J:6200
	brachyphalangia	J:6200
	cleft secondary palate	J:6200
	decreased caudal vertebrae number	J:6200
	decreased hair follicle number	J:6200
	flat face	J:7243
	flattened snout	J:7243
	fused lips	J:7243
	herniated intestine	J:6200
	kyphosis	J:6200
	median cleft palate	J:6200
	microcephaly	J:7243
	microphthalmia	J:6200, J:7243
	neonatal lethality, complete penetrance	J:6200
	oral atresia	J:6200
	palatal shelf fusion with tongue or mandible	J:7243
	respiratory distress	J:6200
	respiratory failure	J:6200
	shiny skin	J:6200
	short limbs	J:6200
	short snout	J:6200
	small ears	J:6200, J:7243
	small external nares	J:6200, J:7243
	thin lip	J:6200
	thin skin	J:6200, J:6708
SfnEr/SfnEr involves: C57BL/6By	abnormal apical ectodermal ridge morphology	J:148459
	abnormal craniofacial development	J:148459
	abnormal embryonic autopod plate morphology	J:148459
	abnormal epidermal layer morphology	J:148459
	abnormal epidermis stratum basale morphology	J:148459
	abnormal epidermis stratum spinosum morphology	J:148459
	abnormal eyelid aperture	J:148460
	abnormal eyelid fusion	J:148460
	abnormal eyelid morphology	J:148460
	abnormal limb bud morphology	J:148459
	abnormal limb development	J:148459
	abnormal tail morphology	J:148459
	distorted hair follicle pattern	J:148459
	fused lips	J:148459
	kinked tail	J:148459
	microphthalmia	J:148459
	short tail	J:148459
	small limb buds	J:148459
	syndactyly	J:148459
	thick epidermis	J:148459
	thin epidermis	J:148459
SfnEr/SfnEr Not Specified	normal craniofacial phenotype	J:184926
Sfntm1Mak/Sfntm1Mak involves: 129P2/OlaHsd * C57BL/6	abnormal B cell differentiation	J:168328
	abnormal spleen B cell follicle morphology	J:168328
	abnormal spleen morphology	J:168328
	absent spleen marginal zone	J:168328
	decreased B cell number	J:168328
	decreased B-1a cell number	J:168328
	decreased follicular B cell number	J:168328
	decreased IgG level	J:168328
	decreased IgM level	J:168328
	decreased marginal zone B cell number	J:168328
	normal immune system phenotype	J:168328
	increased B cell apoptosis	J:168328
	increased B cell proliferation	J:168328
	increased susceptibility to Riboviria infection	J:168328
	increased susceptibility to Riboviria infection induced morbidity/mortality	J:168328
Sfntm1Mul/Sfntm1Mul involves: 129S1/Sv * 129X1/SvJ * FVB/N	abnormal mammary gland epithelium morphology	J:159517
Sfntm1Mul/Sfntm1Mul Tg(MMTV-cre)7Mul/0 involves: 129S1/Sv * 129X1/SvJ * FVB/N	abnormal cell adhesion	J:159517
	abnormal mammary gland duct morphology	J:159517
	abnormal mammary gland epithelium morphology	J:159517
	increased cell proliferation	J:159517