98 phenotypes from 6 alleles in 10 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Ift172avc1/Ift172avc1 involves: C57BL/6J	abnormal cilium morphology	J:175371
	abnormal kidney morphology	J:175371
	abnormal motile primary cilium morphology	J:175371
	abnormal renal glomerulus morphology	J:175371
	abnormal trachea morphology	J:175371
	anal atresia	J:175371
	atrioventricular septal defect	J:175371
	normal cardiovascular system phenotype	J:175371
	cleft secondary palate	J:175371
	decreased length of long bones	J:175371
	enlarged brain ventricles	J:175371
	esophageal atresia	J:175371
	esophagus hypoplasia	J:175371
	esophagus stenosis	J:175371
	hydrocephaly	J:175371
	perinatal lethality, complete penetrance	J:175371
	preaxial polydactyly	J:175371
	short femur	J:175371
	short fibula	J:175371
	short humerus	J:175371
	short radius	J:175371
	short snout	J:175371
	short tibia	J:175371
	short ulna	J:175371
Ift172avc1/Ift172avc1 involves: C57BL/6J * FVB/N	complete atrioventricular septal defect	J:163196
	increased heart atrium size	J:163196
	increased heart ventricle size	J:163196
	perinatal lethality	J:163196
	preaxial polydactyly	J:163196
Ift172avc1/Ift172wim involves: C57BL/6J	abnormal cardiovascular system morphology	J:175371
	abnormal cilium morphology	J:175371
	abnormal craniofacial morphology	J:175371
	abnormal limb morphology	J:175371
	abnormal motile primary cilium morphology	J:175371
Ift172tm1.1Rama/Ift172tm1.1Rama Tg(Rho-icre)1Ck/0 involves: 129X1/SvJ * C57BL/6 * SJL	abnormal electroretinogram waveform feature	J:262800
	abnormal photoreceptor outer segment disc membrane morphology	J:262800
	abnormal photoreceptor outer segment morphology	J:262800
	decreased b-wave amplitude	J:262800
	disorganized photoreceptor outer segment	J:262800
	photoreceptor outer segment degeneration	J:262800
	retina degeneration	J:262800
	retina outer nuclear layer degeneration	J:262800
	short photoreceptor outer segment	J:262800
Ift172tm1.1Rama/Ift172tm1.1Rama Tg(Stra8-icre)1Reb/0 involves: 129 * 129S4/SvJaeSor * C57BL/6 * FVB/NJ	abnormal acrosome morphology	J:302808
	abnormal cauda epididymis morphology	J:302808
	abnormal centrosome morphology	J:302808
	abnormal outer dense fiber morphology	J:302808
	abnormal seminiferous tubule morphology	J:302808
	abnormal sperm axoneme morphology	J:302808
	abnormal sperm flagellum morphology	J:302808
	abnormal sperm head morphology	J:302808
	abnormal sperm midpiece morphology	J:302808
	abnormal sperm physiology	J:302808
	abnormal spermatid morphology	J:302808
	abnormal spermiation	J:302808
	abnormal spermiogenesis	J:302808
	asthenozoospermia	J:302808
	decreased litter size	J:302808
	ectopic manchette	J:302808
	elongated manchette	J:302808
	kinked sperm flagellum	J:302808
	oligozoospermia	J:302808
	reduced male fertility	J:302808
	small seminiferous tubules	J:302808
	teratozoospermia	J:302808
Ift172tm1.1Rama/Ift172tm1.2Rama Tg(Prrx1-cre)1Cjt/0 involves: 129S4/SvJaeSor * 129X1/SvJ * C57BL/6 * SJL/J	polydactyly	J:156426
	short limbs	J:156426
Ift172tm1.2Rama/Ift172tm1.2Rama involves: 129S4/SvJaeSor * 129X1/SvJ * BALB/c * C57BL/6	abnormal embryo development	J:156426
	abnormal neural tube morphology	J:156426
	prenatal lethality, complete penetrance	J:156426
Ift172tm1Lmgd/Ift172tm1Lmgd involves: 129S1/Sv * 129X1/SvJ * C57BL/6	abnormal brain development	J:143572
	abnormal cardiac outflow tract development	J:143572
	abnormal diencephalon morphology	J:143572
	abnormal direction of heart looping	J:143572
	abnormal embryonic neuroepithelium morphology	J:143572
	abnormal left-right axis patterning	J:143572
	abnormal mesendoderm development	J:143572
	abnormal rhombomere morphology	J:143572
	abnormal telencephalon morphology	J:143572
	anophthalmia	J:143572
	decreased heart right ventricle size	J:143572
	edema	J:143572
	embryonic lethality during organogenesis, complete penetrance	J:143572
	exencephaly	J:143572
	hemorrhage	J:143572
	holoprosencephaly	J:143572
	open neural tube	J:143572
	polydactyly	J:143572
Ift172tm2b(EUCOMM)Hmgu/Ift172+ C57BL/6N-Ift172tm2b(EUCOMM)Hmgu/Bay	abnormal digit morphology	J:211773
	abnormal retina blood vessel morphology	J:211773
Ift172tm2b(EUCOMM)Hmgu/Ift172tm2b(EUCOMM)Hmgu C57BL/6N-Ift172tm2b(EUCOMM)Hmgu/Bay	abnormal allantois morphology	J:211773
	abnormal embryo development	J:211773
	abnormal embryo turning	J:211773
	abnormal heart morphology	J:211773
	abnormal neural tube closure	J:211773
	abnormal pericardium morphology	J:211773
	abnormal pharyngeal arch morphology	J:211773
	edema	J:211773
	embryonic growth retardation	J:211773
	embryonic lethality prior to tooth bud stage	J:211773
	hemorrhage	J:211773
	preweaning lethality, complete penetrance	J:211773
Ift172wim/Ift172wim C3.B6J-Ift172wim	abnormal direction of heart looping	J:86437
	abnormal floor plate morphology	J:86437
	absent embryonic cilia	J:86437
	embryonic lethality during organogenesis, complete penetrance	J:86437
	open neural tube	J:86437
Ift172wim/Ift172wim 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
	exencephaly	J:98216
Ift172wim/Ift172wim involves: C57BL/6J	abnormal cilium morphology	J:138139