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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Ift88tm1.1Bky
targeted mutation 1.1, Bradley K Yoder
MGI:3710186
Summary 5 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Ift88tm1.1Bky/Ift88tm1.1Bky involves: 129P2/OlaHsd MGI:7519154
ht2
Ift88tm1Rpw/Ift88tm1.1Bky involves: 129 * 129P2/OlaHsd MGI:3710955
ht3
Ift88cbbs/Ift88tm1.1Bky involves: 129P2/OlaHsd * 129S4/SvJae * C57BL/6 MGI:3823202
cn4
Ift88tm1Bky/Ift88tm1.1Bky involves: 129P2/OlaHsd MGI:3710954
cn5
Ift88tm1Bky/Ift88tm1.1Bky
Tg(Prrx1-cre)1Cjt/?
involves: 129P2/OlaHsd * C57BL/6J * SJL/J MGI:3710956


Genotype
MGI:7519154
hm1
Allelic
Composition
Ift88tm1.1Bky/Ift88tm1.1Bky
Genetic
Background
involves: 129P2/OlaHsd
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Ift88tm1.1Bky mutation (0 available); any Ift88 mutation (48 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• embryos are arrested at stage E9.5

embryo

cardiovascular system

homeostasis/metabolism

cellular




Genotype
MGI:3710955
ht2
Allelic
Composition
Ift88tm1Rpw/Ift88tm1.1Bky
Genetic
Background
involves: 129 * 129P2/OlaHsd
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Ift88tm1.1Bky mutation (0 available); any Ift88 mutation (48 available)
Ift88tm1Rpw mutation (0 available); any Ift88 mutation (48 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
nervous system
• at E11.5, the neural tube is misaligned
• at E11.5, the neural tube is not closed

cardiovascular system
• at E11.5, the cardiac sac balloons

embryo
• at E11.5, the neural tube is misaligned
• at E11.5, the neural tube is not closed




Genotype
MGI:3823202
ht3
Allelic
Composition
Ift88cbbs/Ift88tm1.1Bky
Genetic
Background
involves: 129P2/OlaHsd * 129S4/SvJae * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Ift88cbbs mutation (0 available); any Ift88 mutation (48 available)
Ift88tm1.1Bky mutation (0 available); any Ift88 mutation (48 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
nervous system
• enlarged midbrain
• at E11.5, the telencephalon is shortened along its rostral-caudal axis compared to in wild-type mice
• at E11.5, the dorsal telencephalic midline is barely invaginated, the cortical ventricular zone is reduced to a thin strip, and the medial and lateral ganglionic eminences are reduced in size

cardiovascular system
• 3 of 7 mice exhibit a rightward-looping heart tube

vision/eye
• bilaterally in all mice




Genotype
MGI:3710954
cn4
Allelic
Composition
Ift88tm1Bky/Ift88tm1.1Bky
Genetic
Background
involves: 129P2/OlaHsd
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Ift88tm1.1Bky mutation (0 available); any Ift88 mutation (48 available)
Ift88tm1Bky mutation (1 available); any Ift88 mutation (48 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
limbs/digits/tail
• at E11.5, the ventral (but not the dorsal) ectoderm of the limb bud is nearly devoid of cilia
• however, normal limbs form

embryo
• at E11.5, the ventral (but not the dorsal) ectoderm of the limb bud is nearly devoid of cilia
• however, normal limbs form




Genotype
MGI:3710956
cn5
Allelic
Composition
Ift88tm1Bky/Ift88tm1.1Bky
Tg(Prrx1-cre)1Cjt/?
Genetic
Background
involves: 129P2/OlaHsd * C57BL/6J * SJL/J
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Ift88tm1.1Bky mutation (0 available); any Ift88 mutation (48 available)
Ift88tm1Bky mutation (1 available); any Ift88 mutation (48 available)
Tg(Prrx1-cre)1Cjt mutation (2 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
skeleton
• at E18.5, mice display varying severities of endochondral bone defects in all long bones with dramatic reduction in overall length
• mice lack expression of an osteoblast-specific marker (alkaline phosphates) in the perichondrium
• cells adjacent to the perichondrium resemble chondrocytes rather than osteoblast
• at E18.5, proliferating chondrocytes in the growth region of the tibia are round and flat
• at E18.5, only small cilia are occasionally observed on chondrocytes of the developing tibia
• at E18.5, ectopic chondrocytes are seen in the perichondrium
• at E18.5, perichondrial cells are disorganized, do not adopt the characteristic flattened morphology and are not evenly distributed along the bone
• at E18.5, bone collar formation is absent in the tibia
• at E18.5, some cells in the perichondrium appear to be differentiating into chondrocytes rather than into osteoblasts
• at E18.5, bone vascularization is delayed and hypertrophic cells persist
• at E18.5, the growth region of the tibia contains only a small disorganized area of round and flat proliferating chondrocytes
• at E18.5, the growth region of the tibia contains only a small disorganized area of round and flat proliferating chondrocytes
• only some regions of the tibia contain mineralized bone

limbs/digits/tail
• at E11.5, very few cells with cilia are present in the limb mesenchyme
• however, cilia of the overlying ectoderm is normal
• at E18.5, mice have 8 or more non-patterned digits on their forelimbs while each hindlimb has a single extra preaxial digit (typically a duplication of digit 1)
• at E13.5 and P11, all four limbs are shortened in the proximodistal axis
• however, limb patterning is normal

growth/size/body
• mice are smaller postnatally

embryo
• at E11.5, very few cells with cilia are present in the limb mesenchyme
• however, cilia of the overlying ectoderm is normal





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last database update
11/12/2024
MGI 6.24
The Jackson Laboratory