66 phenotypes from 3 alleles in 3 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Ift27tm1a(EUCOMM)Hmgu/Ift27tm1a(EUCOMM)Hmgu involves: C57BL/6N	abnormal hair follicle development	J:224085
	abnormal keratinocyte differentiation	J:224085
	absent hair follicles	J:224085
	normal cellular phenotype	J:224085
	decreased keratinocyte proliferation	J:224085
	normal integument phenotype	J:224085
	neonatal lethality, complete penetrance	J:224085
	small hair follicles	J:224085
	underdeveloped hair follicles	J:224085
Ift27tm1b(EUCOMM)Hmgu/Ift27tm1b(EUCOMM)Hmgu involves: 129S4/SvJae * C57BL/6J * C57BL/6N	abdominal situs ambiguus	J:215449
	abnormal aortic arch morphology	J:215449
	abnormal atrioventricular cushion morphology	J:215449
	abnormal blood vessel morphology	J:215449
	abnormal incisor morphology	J:215449
	abnormal jaw morphology	J:215449
	abnormal limb morphology	J:215449
	abnormal lung morphology	J:215449
	abnormal lung position or orientation	J:215449
	abnormal mouth morphology	J:215449
	abnormal nasal septum morphology	J:215449
	abnormal nose morphology	J:215449
	abnormal palate morphology	J:215449
	abnormal rib morphology	J:215449
	abnormal tongue morphology	J:215449
	abnormal trachea morphology	J:215449
	abnormal vomeronasal organ morphology	J:215449
	absent tongue	J:215449
	common atrium	J:215449
	cyanosis	J:215449
	decreased tongue size	J:215449
	double aortic arch	J:215449
	double outlet right ventricle with atrioventricular septal defect	J:215449
	dual inferior vena cava	J:215449
	lung cyst	J:215449
	micrognathia	J:215449
	midface hypoplasia	J:215449
	misaligned sternebrae	J:215449
	ocular hypotelorism	J:215449
	omphalocele	J:215449
	perinatal lethality, incomplete penetrance	J:215449
	pulmonary trunk hypoplasia	J:215449
	small mandible	J:215449
	umbilical hernia	J:215449
Ift27tm1c(EUCOMM)Hmgu/Ift27tm1c(EUCOMM)Hmgu Tg(Stra8-icre)1Reb/0 involves: 129S4/SvJae * C57BL/6J * C57BL/6N * FVB/NJ	abnormal outer dense fiber morphology	J:251964
	abnormal plasma membrane morphology	J:251964
	abnormal sperm axoneme morphology	J:251964
	abnormal sperm end piece morphology	J:251964
	abnormal sperm fibrous sheath morphology	J:251964
	abnormal sperm flagellum morphology	J:251964
	abnormal sperm flagellum thickness	J:251964
	abnormal sperm head morphology	J:251964
	abnormal sperm mitochondrial sheath morphology	J:251964
	abnormal spermatogenesis	J:251964
	abnormal spermiation	J:251964
	abnormal testis physiology	J:251964
	arrest of spermiogenesis	J:251964
	asthenozoospermia	J:251964
	decreased sperm progressive motility	J:251964
	globozoospermia	J:251964
	immotile sperm	J:251964
	kinked sperm flagellum	J:251964
	male infertility	J:251964
	oligozoospermia	J:251964
	normal reproductive system phenotype	J:251964
	short sperm flagellum	J:251964
	teratozoospermia	J:251964