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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID 		Ift172
intraflagellar transport 172
MGI:2682064
98 phenotypes from 6 alleles in 10 genetic backgrounds
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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
Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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Send questions and comments to User Support. 		last database update
12/10/2024
MGI 6.24 		The Jackson Laboratory