104 phenotypes from 4 alleles in 10 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Kif3a2a/Kif3a2a involves: C3HeB/FeJ * C57BL/6J	abnormal left-right axis patterning	J:98216
	abnormal spinal cord morphology	J:98216
	embryonic lethality during organogenesis, complete penetrance	J:98216
Kif3atm1Gsn/Kif3a+ involves: 129S1/Sv * 129X1/SvJ	abnormal embryo turning	J:54575
	abnormal heart looping	J:54575
	decreased embryo size	J:54575
	pericardial edema	J:54575
Kif3atm1Gsn/Kif3atm1Gsn involves: 129S1/Sv * 129X1/SvJ	abnormal direction of heart looping	J:54575
	abnormal embryo turning	J:54575
	abnormal heart looping	J:54575
	abnormal left-right axis patterning	J:54575
	abnormal limb development	J:54575
	abnormal neural tube closure	J:54575
	abnormal primitive node morphology	J:54575
	absent embryonic cilia	J:54575
	caudal body truncation	J:54575
	decreased embryo size	J:54575
	delayed heart looping	J:54575
	embryonic lethality during organogenesis, complete penetrance	J:54575
	pericardial edema	J:54575
	situs inversus	J:54575
	small pharyngeal arch	J:54575
Kif3atm1Gsn/Kif3atm2Gsn involves: 129S1/Sv * 129X1/SvJ * C57BL/6J * SJL/J	decreased body size	J:117033
	decreased length of long bones	J:117033
	decreased long bone epiphyseal plate size	J:117033
	disorganized long bone epiphyseal plate	J:117033
	polydactyly	J:117033
	short limbs	J:117033
Kif3atm1Gsn/Kif3atm2Gsn Tg(Cdh16-cre)91Igr/0 involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * ICR	absent kidney epithelial cell primary cilium	J:83293
	enlarged kidney	J:83293
	increased blood urea nitrogen level	J:83293
	increased kidney apoptosis	J:83293
	kidney cortex cyst	J:83293
	kidney cyst	J:83293
	kidney failure	J:83293
	kidney medulla cyst	J:83293
	lethargy	J:83293
	polycystic kidney	J:83293
	postnatal growth retardation	J:83293
	renal interstitial fibrosis	J:83293
	renal tubule atrophy	J:83293
Kif3atm1Gsn/Kif3atm2Gsn Tg(FOXJ1-cre/ERT2)1Blh/0 involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * DBA	abnormal brain morphology	J:174694
Kif3atm1Gsn/Kif3atm2Gsn Tg(Msx2-cre)5Rem/? involves: 129S1/Sv * 129X1/SvJ	abnormal limb bud morphology	J:117033
Kif3atm1Noh/Kif3atm1Noh involves: 129S4/SvJae * C57BL/6J	abnormal developmental patterning	J:55332
	abnormal direction of heart looping	J:55332
	abnormal heart looping	J:55332
	abnormal left-right axis patterning	J:55332
	abnormal mesoderm development	J:55332
	abnormal somite development	J:55332
	absent embryonic cilia	J:55332
	absent nodal flow	J:55332
	decreased embryo size	J:55332
	distended pericardium	J:55332
	embryonic lethality during organogenesis, complete penetrance	J:55332
	hydrocephaly	J:55332
	incomplete embryo turning	J:55332
	myocardium hypoplasia	J:55332
	neural tube degeneration	J:55332
	pericardial effusion	J:55332
	wavy neural tube	J:55332
Kif3atm2Gsn/Kif3atm2Gsn H2az2Tg(Wnt1-cre)11Rth/H2az2+ involves: 129S1/Sv * 129X1/SvJ * C57BL/6J * CBA/J	abnormal basisphenoid bone morphology	J:158523
	abnormal cranial neural crest cell morphology	J:158523
	abnormal craniofacial bone morphology	J:158523
	abnormal craniofacial development	J:158523
	abnormal cranium morphology	J:158523
	abnormal frontal bone morphology	J:158523
	abnormal maxilla morphology	J:158523
	abnormal nasal bone morphology	J:158523
	abnormal nasal septum morphology	J:158523
	abnormal palatine bone morphology	J:158523
	abnormal premaxilla morphology	J:158523
	absent corpus callosum	J:158523
	absent mandibular condyloid process	J:158523
	absent mandibular ramus	J:158523
	anterior cranium occultum	J:158523
	broad frontonasal prominence	J:158523
	cleft secondary palate	J:158523
	increased cranial neural crest cell proliferation	J:158523
	ocular hypertelorism	J:158523
	short mandible	J:158523
Kif3atm2Gsn/Kif3atm2Gsn Tg(Col2a1-cre)1Bhr/? involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * SJL	abnormal actin cytoskeleton morphology	J:121342
	abnormal chondrocyte morphology	J:121342
	abnormal long bone epiphyseal plate morphology	J:121342
	abnormal long bone epiphyseal plate proliferative zone	J:121342
	abnormal long bone epiphysis morphology	J:121342
	abnormal long bone hypertrophic chondrocyte zone	J:121342
	abnormal rib morphology	J:121342
	decreased length of long bones	J:121342
	disproportionate dwarf	J:121342
	spina bifida occulta	J:121342
	thoracic vertebral fusion	J:121342
Kif3atm2Gsn/Kif3atm2Gsn Tg(Col2a1-cre)10Amc/0 involves: 129S1/Sv * 129X1/SvJ * C57BL/6	abnormal basicranium morphology	J:140779
	abnormal endochondral bone ossification	J:140779
	disorganized long bone epiphyseal plate	J:140779
	disproportionate dwarf	J:140779
	polycystic kidney	J:140779
Kif3atm2Gsn/Kif3atm2Gsn Tg(NEUROG3-cre)1Herr/0 involves: 129S1/Sv * 129X1/SvJ * C57BL/6	abnormal cauda epididymis morphology	J:210780
	abnormal epididymis morphology	J:210780
	abnormal manchette disassembly	J:210780
	abnormal manchette morphology	J:210780
	abnormal manchette perinuclear ring morphology	J:210780
	abnormal outer dense fiber morphology	J:210780
	abnormal sperm axoneme morphology	J:210780
	abnormal sperm fibrous sheath morphology	J:210780
	abnormal sperm flagellum morphology	J:210780
	abnormal sperm head morphology	J:210780
	abnormal sperm mitochondrial sheath morphology	J:210780
	abnormal sperm nucleus morphology	J:210780
	abnormal spermatid morphology	J:210780
	abnormal spermatogenesis	J:210780
	decreased epididymis weight	J:210780
	decreased testis weight	J:210780
	ectopic manchette	J:210780
	elongated manchette	J:210780
	male infertility	J:210780
	oligozoospermia	J:210780
Kif3atm2Gsn/Kif3atm2Gsn Tg(Rbp3-cre)528Jxm/0 involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA	abnormal photoreceptor inner segment morphology	J:63427
	retina photoreceptor degeneration	J:63427
	short photoreceptor inner segment	J:63427
	short photoreceptor outer segment	J:63427