55 phenotypes from 7 alleles in 18 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Nxnem1(IMPC)Bay/Nxn+ C57BL/6N-Nxnem1(IMPC)Bay/Bay	abnormal retina blood vessel morphology	J:211773
	unresponsive to tactile stimuli	J:211773
Nxnem1(IMPC)Bay/Nxnem1(IMPC)Bay C57BL/6N-Nxnem1(IMPC)Bay/Bay	abnormal embryo size	J:211773
	abnormal facial morphology	J:211773
	abnormal head shape	J:211773
	abnormal head size	J:211773
	facial cleft	J:211773
	preweaning lethality, complete penetrance	J:211773
	unresponsive to tactile stimuli	J:211773
Nxnem1(IMPC)J/Nxn+ C57BL/6NJ-Nxnem1(IMPC)J/J	increased fasting circulating glucose level	J:211773
	increased mean corpuscular hemoglobin concentration	J:211773
Nxnem1(IMPC)J/Nxnem1(IMPC)J C57BL/6NJ-Nxnem1(IMPC)J/J	abnormal embryo size	J:211773
	abnormal facial morphology	J:211773
	cleft palate	J:211773
	facial cleft	J:211773
	preweaning lethality, complete penetrance	J:211773
Nxnem1(IMPC)Mbp/Nxn+ C57BL/6N-Nxnem1(IMPC)Mbp/Ucd	decreased body length	J:211773
Nxnem1(IMPC)Mbp/Nxnem1(IMPC)Mbp C57BL/6N-Nxnem1(IMPC)Mbp/Ucd	preweaning lethality, complete penetrance	J:211773
Nxnl11Jus13/Nxnl11Jus13 Not Specified	perinatal lethality, complete penetrance	J:109155
Nxntm1a(EUCOMM)Wtsi/Nxn+ C57BL/6N-Nxntm1a(EUCOMM)Wtsi/Bay	abnormal retina blood vessel morphology	J:211773
	anophthalmia	J:211773
	decreased cardiac muscle contractility	J:211773
	irregularly shaped pupil	J:211773
Nxntm1a(EUCOMM)Wtsi/Nxn+ C57BL/6N-Nxntm1a(EUCOMM)Wtsi/Ieg	increased grip strength	J:165965
Nxntm1a(EUCOMM)Wtsi/Nxntm1a(EUCOMM)Wtsi C57BL/6N-Nxntm1a(EUCOMM)Wtsi/Bay	preweaning lethality, incomplete penetrance	J:211773
Nxntm1b(EUCOMM)Wtsi/Nxn+ C57BL/6N-Nxntm1b(EUCOMM)Wtsi/Bay	unresponsive to tactile stimuli	J:211773
Nxntm1b(EUCOMM)Wtsi/Nxn+ C57BL/6N-Nxntm1b(EUCOMM)Wtsi/Ccpcz	abnormal mammary gland morphology	J:211773
	increased circulating HDL cholesterol level	J:211773
	increased circulating triglyceride level	J:211773
	increased effector memory CD8-positive, alpha-beta T cell number	J:211773
Nxntm1b(EUCOMM)Wtsi/Nxn+ C57BL/6N-Nxntm1b(EUCOMM)Wtsi/H	abnormal snout morphology	J:211773
Nxntm1b(EUCOMM)Wtsi/Nxn+ C57BL/6N-Nxntm1b(EUCOMM)Wtsi/Ics	abnormal digit morphology	J:211773
	abnormal freezing behavior	J:211773
	abnormal locomotor behavior	J:211773
	decreased exploration in new environment	J:211773
	decreased locomotor activity	J:211773
	increased circulating alkaline phosphatase level	J:211773
Nxntm1b(EUCOMM)Wtsi/Nxn+ C57BL/6N-Nxntm1b(EUCOMM)Wtsi/MbpMmucd	microcephaly	J:211773
	short tibia	J:211773
	syndactyly	J:211773
Nxntm1b(EUCOMM)Wtsi/Nxn+ C57BL/6N-Nxntm1b(EUCOMM)Wtsi/Nju	abnormal optic disk morphology	J:211773
Nxntm1b(EUCOMM)Wtsi/Nxn+ C57BL/6N-Nxntm1b(EUCOMM)Wtsi/Rbrc	short tibia	J:211773
Nxntm1b(EUCOMM)Wtsi/Nxn+ C57BL/6N-Nxntm1b(EUCOMM)Wtsi/Ucd	small adrenal glands	J:211773
Nxntm1b(EUCOMM)Wtsi/Nxn+ C57BL/6N-Nxntm1b(EUCOMM)Wtsi/Wtsi	abnormal cranium morphology	J:211773
	abnormal eyelid morphology	J:211773
	abnormal snout morphology	J:211773
Nxntm1b(EUCOMM)Wtsi/Nxntm1b(EUCOMM)Wtsi C57BL/6N-Nxntm1b(EUCOMM)Wtsi/Bay	abnormal embryo size	J:211773
	abnormal facial morphology	J:211773
	abnormal head shape	J:211773
	abnormal head size	J:211773
	cleft palate	J:211773
	facial cleft	J:211773
	preweaning lethality, complete penetrance	J:211773
	unresponsive to tactile stimuli	J:211773
Nxntm1b(EUCOMM)Wtsi/Nxntm1b(EUCOMM)Wtsi C57BL/6N-Nxntm1b(EUCOMM)Wtsi/Ccpcz	abnormal facial morphology	J:211773
	abnormal head shape	J:211773
	no spontaneous movement	J:211773
	preweaning lethality, complete penetrance	J:211773
Nxntm1b(EUCOMM)Wtsi/Nxntm1b(EUCOMM)Wtsi C57BL/6N-Nxntm1b(EUCOMM)Wtsi/H	preweaning lethality, complete penetrance	J:211773
Nxntm1b(EUCOMM)Wtsi/Nxntm1b(EUCOMM)Wtsi C57BL/6N-Nxntm1b(EUCOMM)Wtsi/Ics	preweaning lethality, complete penetrance	J:211773
Nxntm1b(EUCOMM)Wtsi/Nxntm1b(EUCOMM)Wtsi C57BL/6N-Nxntm1b(EUCOMM)Wtsi/Ieg	preweaning lethality, complete penetrance	J:211773
Nxntm1b(EUCOMM)Wtsi/Nxntm1b(EUCOMM)Wtsi C57BL/6N-Nxntm1b(EUCOMM)Wtsi/J	abnormal craniofacial morphology	J:211773
	abnormal embryo size	J:211773
	abnormal facial morphology	J:211773
	cleft palate	J:211773
	preweaning lethality, complete penetrance	J:211773
Nxntm1b(EUCOMM)Wtsi/Nxntm1b(EUCOMM)Wtsi C57BL/6N-Nxntm1b(EUCOMM)Wtsi/MbpMmucd	microcephaly	J:211773
	preweaning lethality, complete penetrance	J:211773
	syndactyly	J:211773
Nxntm1b(EUCOMM)Wtsi/Nxntm1b(EUCOMM)Wtsi C57BL/6N-Nxntm1b(EUCOMM)Wtsi/Nju	preweaning lethality, complete penetrance	J:211773
Nxntm1b(EUCOMM)Wtsi/Nxntm1b(EUCOMM)Wtsi C57BL/6N-Nxntm1b(EUCOMM)Wtsi/Rbrc	preweaning lethality, complete penetrance	J:211773
Nxntm1b(EUCOMM)Wtsi/Nxntm1b(EUCOMM)Wtsi C57BL/6N-Nxntm1b(EUCOMM)Wtsi/Ucd	abnormal craniofacial morphology	J:211773
	preweaning lethality, complete penetrance	J:211773
Nxntm1b(EUCOMM)Wtsi/Nxntm1b(EUCOMM)Wtsi C57BL/6N-Nxntm1b(EUCOMM)Wtsi/Wtsi	abnormal Mullerian duct morphology	J:239583
	abnormal vitelline vein topology	J:239583
	absent stapedial artery	J:239583
	cleft palate	J:239583
	decreased intestine length	J:239583
	dilated liver sinusoidal space	J:239583
	double outlet right ventricle	J:239583
	herniated liver	J:239583
	perimembraneous ventricular septal defect	J:239583
	preweaning lethality, complete penetrance	J:211773
Nxntm1Hmik/Nxntm1Hmik involves: 129P2/OlaHsd * C57BL/6J	abnormal cell physiology	J:167570
	abnormal sternum morphology	J:167570
	atrioventricular septal defect	J:167570
	decreased fetal size	J:167570
	increased osteoblast cell number	J:167570
	perinatal lethality, complete penetrance	J:167570
	persistent truncus arteriosus	J:167570
	small frontal bone	J:167570
	split xiphoid process	J:167570
	ventricular septal defect	J:167570