62 phenotypes from 6 alleles in 11 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Jam3tm1.1(KOMP)Vlcg/Jam3+ C57BL/6N-Jam3tm1.1(KOMP)Vlcg/J	abnormal skeletal muscle morphology	J:211773
	abnormal sleep behavior	J:211773
	decreased fasting circulating glucose level	J:211773
Jam3tm1.1(KOMP)Vlcg/Jam3tm1.1(KOMP)Vlcg C57BL/6N-Jam3tm1.1(KOMP)Vlcg/J	male infertility	J:211773
	preweaning lethality, incomplete penetrance	J:211773
Jam3tm1.1Chav/Jam3tm1.1Chav Tg(Tal1-cre/ERT)1Jrg/? involves: 129 * C57BL/6	decreased metastatic potential	J:173391
Jam3tm1.1Chav/Jam3tm1.2Chav Tg(Cdh5-cre)7Mlia/? involves: 129 * C57BL/6 * FVB/N	decreased metastatic potential	J:173391
Jam3tm1.2Chav/Jam3tm1.2Chav B6.129-Jam3tm1.2Chav	decreased metastatic potential	J:173391
	male infertility	J:173391
	prenatal lethality, incomplete penetrance	J:173391
	preweaning lethality, incomplete penetrance	J:173391
Jam3tm1.2Chav/Jam3tm1.2Chav involves: 129 * C57BL/6	male infertility	J:173391
	prenatal lethality, incomplete penetrance	J:173391
	preweaning lethality, incomplete penetrance	J:173391
Jam3tm1Lex/Jam3tm1Lex involves: 129S5/SvEvBrd * C57BL/6	abnormal behavior	J:281813
	azoospermia	J:145994, J:281813
	normal cardiovascular system phenotype	J:281813
	cyanosis	J:145994
	decreased locomotor activity	J:281813
	decreased neutrophil cell number	J:145994
	enlarged esophagus	J:145994, J:281813
	increased bone marrow cell number	J:145994
	increased common myeloid progenitor cell number	J:145994
	increased erythroid progenitor cell number	J:145994
	increased granulocyte number	J:145994
	male infertility	J:145994
	perinatal lethality, incomplete penetrance	J:145994
	postnatal growth retardation	J:281813
	premature death	J:281813
Jam3tm1Rha/Jam3tm1.1Chav Tg(Spo11-cre)D5Mpel/0 involves: 129P2/OlaHsd * BALB/c * C57BL/6	abnormal manchette morphology	J:166888
	abnormal spermatid morphology	J:166888
	arrest of spermatogenesis	J:166888
	decreased male germ cell number	J:166888
	increased male germ cell apoptosis	J:166888
	small testis	J:166888
Jam3tm1Rha/Jam3tm1Rha B6.129P2-Jam3tm1Rha	abnormal cerebral cortex morphology	J:191990
	abnormal cerebral cortex pyramidal cell morphology	J:191990
	abnormal cranium morphology	J:191990
	abnormal gait	J:191990
	abnormal hippocampus morphology	J:191990
	abnormal innervation	J:191990
	abnormal nervous system physiology	J:191990
	cerebellum atrophy	J:191990
	dilated lateral ventricle	J:191990
	disheveled coat	J:191990
	enlarged cranium	J:191990
	gliosis	J:191990
	hydrocephaly	J:191990
	intracranial hemorrhage	J:191990
	intraventricular hemorrhage	J:191990
	lethargy	J:191990
	obstructive hydrocephaly	J:191990
	postnatal growth retardation	J:191990
	postnatal lethality, incomplete penetrance	J:191990
	subarachnoid hemorrhage	J:191990
	thin cerebral cortex	J:191990
	tremors	J:191990
Jam3tm1Rha/Jam3tm1Rha involves: 129P2/OlaHsd * C57BL/6	abnormal digestive system physiology	J:121841
	abnormal respiratory system physiology	J:121841
	abnormal seminiferous tubule morphology	J:92665
	arrest of spermatogenesis	J:92665
	enlarged esophagus	J:121841
	globozoospermia	J:92665
	increased granulocyte number	J:121841
	increased susceptibility to bacterial infection	J:121841
	lung inflammation	J:121841
	male infertility	J:92665, J:121841
	postnatal lethality	J:92665
	postnatal lethality, incomplete penetrance	J:121841
	small testis	J:92665
Jam3tm1Rha/Jam3tm1Rha Tg(Tek-Jam3)1Maal/0 B6.Cg-Jam3tm1Rha Tg(Tek-Jam3)1Maal	hydrocephaly	J:191990
	postnatal lethality, incomplete penetrance	J:191990
Jam3tm1Rha/Jam3tm1Rha Tg(Tek-Jam3)1Maal/? involves: 129P2/OlaHsd * C57BL/6 * C57BL/6J * CBA	enlarged esophagus	J:121841
	normal immune system phenotype	J:121841
	male infertility	J:121841
	normal mortality/aging	J:121841
Tg(Tek-Jam3)1Maal/? B6.Cg-Tg(Tek-Jam3)1Maal	abnormal cellular extravasation	J:99020
	abnormal leukocyte adhesion	J:99020
	abnormal leukocyte physiology	J:99020
	impaired neutrophil chemotaxis	J:99020
	lung inflammation	J:99020
	peritoneal inflammation	J:99020