27 phenotypes from 3 alleles in 4 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Nischedsn/Nischedsn C3H.B6-Nischedsn	abnormal lung-associated mesenchyme development	J:244907
	abnormal middle ear ossicle morphology	J:244907
	abnormal tympanic membrane morphology	J:244907
	decreased body size	J:244907
	decreased body weight	J:244907
	emphysema	J:244907
	normal hearing/vestibular/ear phenotype	J:244907
	impaired hearing	J:244907
	increased or absent threshold for auditory brainstem response	J:244907
	increased susceptibility to otitis media	J:244907
	postnatal growth retardation	J:244907
	postnatal lethality, incomplete penetrance	J:244907
	short snout	J:244907
Nischedsn/NischV33A involves: BALB/c * C3H/HeH * C57BL/6J	increased or absent threshold for auditory brainstem response	J:244907
	increased susceptibility to otitis media	J:244907
Nischtm1b(EUCOMM)Hmgu/Nisch+ C57BL/6N-Nischtm1b(EUCOMM)Hmgu/H	abnormal bone structure	J:211773
	head bobbing	J:211773
	impaired glucose tolerance	J:211773
Nischtm1b(EUCOMM)Hmgu/Nischtm1b(EUCOMM)Hmgu C57BL/6N-Nischtm1b(EUCOMM)Hmgu/H	abnormal behavior	J:211773
	abnormal bone structure	J:211773
	abnormal cranium morphology	J:211773
	abnormal maxilla morphology	J:211773
	abnormal spine curvature	J:211773
	decreased bone mineral content	J:211773
	decreased locomotor activity	J:211773
	decreased thigmotaxis	J:211773
	head bobbing	J:211773
	impaired glucose tolerance	J:211773
	increased circulating cholesterol level	J:211773
	increased circulating HDL cholesterol level	J:211773
	increased circulating phosphate level	J:211773
	increased circulating triglyceride level	J:211773
NischV33A/NischV33A involves: BALB/c * C57BL/6J	impaired hearing	J:244907
	increased susceptibility to otitis media	J:244907