88 phenotypes from 4 alleles in 6 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Ift140b2b1283Clo/Ift140b2b1283Clo C57BL/6J-Ift140b2b1283Clo	abnormal aortic arch morphology	J:175213
	absent spleen	J:175213
	atrioventricular septal defect	J:175213
	cleft palate	J:175213
	kidney cyst	J:175213
	left pulmonary isomerism	J:175213
	persistent truncus arteriosus	J:175213
	polydactyly	J:175213
	right aortic arch	J:175213
Ift140cauli/Ift140cauli involves: C3H/HeH * C57BL/6JAnu	abnormal atrioventricular valve morphology	J:220659
	abnormal costovertebral joint morphology	J:220659
	abnormal craniofacial morphology	J:199856, J:220659
	abnormal digit morphology	J:220659
	abnormal exoccipital bone morphology	J:220659
	abnormal heart looping	J:199856
	abnormal heart ventricle morphology	J:220659
	abnormal interventricular septum morphology	J:220659
	abnormal limb bud morphology	J:220659
	abnormal lung morphology	J:220659
	abnormal maxilla morphology	J:220659
	abnormal mouth morphology	J:220659
	abnormal neural tube closure	J:220659
	abnormal neural tube morphology	J:220659
	abnormal primary cilium morphology	J:220659
	abnormal rib morphology	J:220659
	abnormal somite development	J:220659
	abnormal tricuspid valve morphology	J:220659
	absent alisphenoid bone	J:220659
	absent facial bone	J:220659
	absent neurocranium	J:220659
	absent palatine bone	J:220659
	absent tympanic ring	J:220659
	anophthalmia	J:199856, J:220659
	cervical vertebral fusion	J:220659
	curly tail	J:220659
	exencephaly	J:199856, J:220659
	exostosis	J:220659
	facial bone hypoplasia	J:220659
	forelimb oligodactyly	J:199856, J:220659
	fusion of atlas and occipital bones	J:220659
	heart hemorrhage	J:220659
	hydrops fetalis	J:220659
	lethality throughout fetal growth and development, complete penetrance	J:220659
	lethality throughout fetal growth and development, incomplete penetrance	J:199856
	maxilla hypoplasia	J:220659
	omphalocele	J:220659
	palatal shelf hypoplasia	J:220659
	polydactyly	J:199856, J:220659
	premaxilla hypoplasia	J:220659
	prenatal growth retardation	J:220659
	rib bifurcation	J:220659
	spina bifida	J:199856
Ift140tm1b(KOMP)Wtsi/Ift140tm1b(KOMP)Wtsi B6.B6N-Ift140tm1b(KOMP)Wtsi	embryonic lethality, complete penetrance	J:181533
Ift140tm1b(KOMP)Wtsi/Ift140tm1b(KOMP)Wtsi involves: C57BL/6N	abnormal hindlimb bud morphology	J:220659
	abnormal mouth morphology	J:220659
	embryonic lethality during organogenesis, complete penetrance	J:220659
	exencephaly	J:220659
Ift140tm1b(KOMP)Wtsi/Ift140tm1c(KOMP)Wtsi Tg(Hoxb7-cre)13Amc/? B6J.B6-Ift140tm1b(KOMP)Wtsi/Ift140tm1c(Komp)Wtsi Tg(Hoxb7-cre)13Amc	abnormal kidney collecting duct morphology	J:181533
	abnormal kidney morphology	J:181533
	abnormal kidney physiology	J:181533
	normal cellular phenotype	J:181533
	decreased kidney epithelial cell primary cilium length	J:181533
	dilated kidney collecting duct	J:181533
	increased kidney apoptosis	J:181533
	increased kidney cell proliferation	J:181533
	kidney cortex cyst	J:181533
	kidney cyst	J:181533
	kidney failure	J:181533
	kidney medulla cyst	J:181533
	renal fibrosis	J:181533
Ift140tm1c(KOMP)Wtsi/Ift140tm1c(KOMP)Wtsi Tg(Stra8-icre)1Reb/0 involves: C57BL/6N * FVB/NJ	abnormal manchette morphology	J:285527
	abnormal outer dense fiber morphology	J:285527
	abnormal sperm axoneme morphology	J:285527
	abnormal sperm end piece morphology	J:285527
	abnormal sperm fibrous sheath morphology	J:285527
	abnormal sperm flagellum morphology	J:285527
	abnormal sperm head morphology	J:285527
	abnormal sperm mitochondrial sheath morphology	J:285527
	abnormal sperm nucleus morphology	J:285527
	abnormal spermatid morphology	J:285527
	abnormal spermiation	J:285527
	abnormal spermiogenesis	J:285527
	asthenozoospermia	J:285527
	decreased sperm progressive motility	J:285527
	immotile sperm	J:285527
	impaired fertilization	J:285527
	kinked sperm flagellum	J:285527
	male infertility	J:285527
	oligozoospermia	J:285527
	normal reproductive system phenotype	J:285527
	short sperm flagellum	J:285527
	teratozoospermia	J:285527