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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID 		Fgfr3
fibroblast growth factor receptor 3
MGI:95524
229 phenotypes from 24 alleles in 23 genetic backgrounds
Export: Excel File
Allelic Composition
Genetic Background		 Annotated Term Reference
Fgfr3m1J/Fgfr3m1J
CByJ.Cg-Fgfr3m1J/GrsrJ 		abnormal tail morphology J:178517
abnormal tail position or orientation J:178517
kyphoscoliosis J:178517
kyphosis J:178517
male infertility J:178517
scoliosis J:178517
Fgfr3tm1.1Aomw/Fgfr3+
129S6.129P2-Fgfr3tm1.1Aomw 		abnormal cochlear outer hair cell morphology J:143356
abnormal craniofacial morphology J:143356, J:144356
abnormal cranium morphology J:144356
abnormal Deiters cell morphology J:143356
abnormal maxillary zygomatic process morphology J:144356
abnormal neurocranium morphology J:144356
abnormal organ of Corti morphology J:143356
abnormal organ of Corti supporting cell differentiation J:143356
abnormal palatine bone horizontal plate morphology J:144356
abnormal patterning of the organ of Corti J:143356
abnormal pillar cell morphology J:143356
abnormal sagittal suture morphology J:144356
abnormal snout morphology J:144356
abnormal zygomatic bone morphology J:144356
decreased body size J:144356
decreased bone mineral density of femur J:144356
decreased femur compact bone thickness J:144356
delayed bone ossification J:144356
domed cranium J:144356
impaired hearing J:143356
increased or absent threshold for auditory brainstem response J:143356
malocclusion J:144356
short snout J:144356
small interparietal bone J:144356
small occipital bone J:144356
thin frontal bone J:144356
thin parietal bone J:144356
Fgfr3tm1.1Aomw/Fgfr3+
B6.129P2-Fgfr3tm1.1Aomw 		abnormal coronal suture morphology J:144356
abnormal cranial suture morphology J:144356
abnormal craniofacial morphology J:143356, J:144356
abnormal cranium morphology J:144356
abnormal foramen magnum morphology J:144356
abnormal lambdoid suture morphology J:144356
abnormal neurocranium morphology J:144356
abnormal occipital bone morphology J:144356
abnormal premaxilla morphology J:144356
abnormal snout morphology J:144356
decreased cranium height J:144356
enlarged interparietal bone J:144356
impaired hearing J:143356
increased or absent threshold for auditory brainstem response J:143356
malocclusion J:144356
short snout J:144356
synostosis J:144356
thin frontal bone J:144356
thin parietal bone J:144356
Fgfr3tm1.1Aomw/Fgfr3+
C.129P2-Fgfr3tm1.1Aomw 		abnormal craniofacial morphology J:143356
normal craniofacial phenotype J:144356
impaired hearing J:143356
increased or absent threshold for auditory brainstem response J:143356
Fgfr3tm1.1Aomw/Fgfr3+
CBACa.129P2-Fgfr3tm1.1Aomw 		abnormal cranium morphology J:144356
abnormal snout morphology J:144356
normal craniofacial phenotype J:143356, J:144356
impaired hearing J:143356
increased or absent threshold for auditory brainstem response J:143356
malocclusion J:144356
short snout J:144356
Fgfr3tm1.1Aomw/Fgfr3tm1.1Aomw
129S6.129P2-Fgfr3tm1.1Aomw 		abnormal cochlear outer hair cell morphology J:143356
abnormal craniofacial morphology J:143356, J:144356
abnormal cranium morphology J:144356
abnormal Deiters cell morphology J:143356
abnormal maxillary zygomatic process morphology J:144356
abnormal neurocranium morphology J:144356
abnormal organ of Corti morphology J:143356
abnormal organ of Corti supporting cell differentiation J:143356
abnormal palatine bone horizontal plate morphology J:144356
abnormal patterning of the organ of Corti J:143356
abnormal pillar cell morphology J:143356
abnormal premaxilla morphology J:144356
abnormal sagittal suture morphology J:144356
abnormal snout morphology J:144356
abnormal zygomatic bone morphology J:144356
decreased body size J:144356
decreased bone mineral density of femur J:144356
decreased cranium height J:144356
decreased femur compact bone thickness J:144356
delayed bone ossification J:144356
domed cranium J:144356
impaired hearing J:143356
increased cranium width J:144356
increased or absent threshold for auditory brainstem response J:143356
malocclusion J:144356
maxillary retrognathia J:144356
ocular hypertelorism J:144356
short nasal bone J:144356
short snout J:144356
small interparietal bone J:144356
small occipital bone J:144356
thin frontal bone J:144356
thin parietal bone J:144356
Fgfr3tm1.1Aomw/Fgfr3tm1.1Aomw
B6.129P2-Fgfr3tm1.1Aomw 		abnormal craniofacial morphology J:143356, J:144356
abnormal cranium morphology J:144356
abnormal snout morphology J:144356
impaired hearing J:143356
increased or absent threshold for auditory brainstem response J:143356
malocclusion J:144356
short snout J:144356
Fgfr3tm1.1Aomw/Fgfr3tm1.1Aomw
C.129P2-Fgfr3tm1.1Aomw 		abnormal craniofacial morphology J:143356
normal craniofacial phenotype J:144356
Fgfr3tm1.1Aomw/Fgfr3tm1.1Aomw
CBACa.129P2-Fgfr3tm1.1Aomw 		abnormal craniofacial morphology J:143356, J:144356
abnormal cranium morphology J:144356
abnormal snout morphology J:144356
impaired hearing J:143356
increased or absent threshold for auditory brainstem response J:143356
malocclusion J:144356
short snout J:144356
Fgfr3tm1.1Iwa/Fgfr3+
involves: 129S6/SvEvTac * FVB/N * NIH Black Swiss 		abnormal chondrocyte differentiation J:70061
abnormal chondrocyte morphology J:70061
abnormal chondrocyte proliferation J:70061
abnormal costal cartilage morphology J:70061
abnormal epiphyseal plate morphology J:70061
abnormal hyaline cartilage morphology J:70061
abnormal long bone epiphyseal plate morphology J:70061
abnormal long bone epiphyseal plate proliferative zone J:70061
abnormal long bone hypertrophic chondrocyte zone J:70061
abnormal spine curvature J:70061
abnormal sternum ossification J:70061
decreased length of long bones J:70061
delayed bone ossification J:70061
disproportionate dwarf J:70061
increased hyoid bone size J:70061
malocclusion J:70061
premature death J:70061
round head J:70061
short limbs J:70061
small thoracic cage J:70061
Fgfr3tm1.1Iwa/Fgfr3tm1.1Iwa
involves: 129S6/SvEvTac * FVB/N * NIH Black Swiss 		prenatal lethality, complete penetrance J:70061
Fgfr3tm1.1Iwa/Fgfr3tm1.1Iwa
involves: 129S6/SvEvTac * NIH Black Swiss * CD-1 * FVB/N 		prenatal lethality, complete penetrance J:70061
Fgfr3tm1Cxd/Fgfr3+
involves: 129S6/SvEvTac * NIH Black Swiss 		decreased body size J:52438
decreased body weight J:52438
short tail J:52438
Fgfr3tm1Cxd/Fgfr3tm1Cxd
involves: 129S6/SvEvTac * NIH Black Swiss 		abnormal chondrocyte morphology J:52438
abnormal long bone epiphyseal plate morphology J:52438
abnormal long bone epiphyseal plate proliferative zone J:52438
abnormal skeleton morphology J:52438
decreased body weight J:52438
decreased width of hypertrophic chondrocyte zone J:52438
disproportionate dwarf J:52438
increased long bone epiphyseal plate size J:52438
megacephaly J:52438
short femur J:52438
short humerus J:52438
short tail J:52438
short vertebral body J:52438
short vertebral column J:52438
Fgfr3tm1Dor/Fgfr3tm1Dor
C3.129S6(B6)-Fgfr3tm1Dor 		abnormal intervertebral disk morphology J:244595
abnormal trabecular bone morphology J:244595
abnormal vertebrae morphology J:244595
decreased bone mineral density J:244595
decreased bone volume J:244595
kyphoscoliosis J:244595
Fgfr3tm1Dor/Fgfr3tm1Dor
CBACa.129S6(B6)-Fgfr3tm1Dor 		abnormal cochlear hair cell morphology J:117235
abnormal cochlear sensory epithelium morphology J:117235
abnormal pillar cell differentiation J:117235
absent pillar cells J:117235
absent tunnel of Corti J:117235
increased cochlear outer hair cell number J:117235
increased Deiters cell number J:117235
increased or absent threshold for auditory brainstem response J:117235
sensorineural hearing loss J:117235
Fgfr3tm1Dor/Fgfr3tm1Dor
involves: 129S6/SvEvTac 		abnormal axial skeleton morphology J:109505
abnormal long bone epiphyseal plate morphology J:109505
increased width of hypertrophic chondrocyte zone J:109505
long femur J:109505
long humerus J:109505
long radius J:109505
long ulna J:109505
normal nervous system phenotype J:118802, J:122940
Fgfr3tm1Dor/Fgfr3tm1Dor
involves: 129S6/SvEvTac * C57BL/6 		abnormal axial skeleton morphology J:32991
abnormal cochlea morphology J:32991
abnormal cochlear OHC efferent innervation pattern J:32991
abnormal cochlear outer hair cell morphology J:32991
abnormal femur morphology J:32991
abnormal humerus morphology J:32991
abnormal long bone hypertrophic chondrocyte zone J:32991
abnormal long bone morphology J:32991
abnormal organ of Corti morphology J:32991
abnormal pillar cell differentiation J:32991
abnormal rib morphology J:32991
absent gastric milk in neonates J:32991
absent pillar cells J:32991
absent tunnel of Corti J:32991
bowed femur J:32991
bowed humerus J:32991
deafness J:32991
decreased body weight J:32991
enlarged vertebral body J:32991
increased Deiters cell number J:32991
increased long bone epiphyseal plate size J:32991
increased or absent threshold for auditory brainstem response J:32991
increased width of hypertrophic chondrocyte zone J:32991
kinked tail J:32991
kyphosis J:32991
long femur J:32991
postnatal lethality, incomplete penetrance J:32991
premature death J:32991
scoliosis J:32991
sensorineural hearing loss J:32991
small thoracic cavity J:32991
Fgfr3tm1Led/Fgfr3tm1Led
involves: 129S6/SvEvTac 		abnormal axial skeleton morphology J:32105
abnormal epiphyseal plate morphology J:32105
abnormal femur morphology J:32105
abnormal fibula morphology J:32105
abnormal gait J:32105
abnormal long bone epiphyseal plate proliferative zone J:32105
abnormal long bone hypertrophic chondrocyte zone J:32105
abnormal long bone morphology J:32105
abnormal spine curvature J:32105
abnormal tail morphology J:32105
abnormal thoracic vertebrae morphology J:32105
abnormal tibia morphology J:32105
abnormal vertebrae morphology J:32105
abnormal vertebral epiphyseal plate morphology J:32105
bowed femur J:32105
decreased body size J:32105
elongated vertebral body J:32105
increased bone ossification J:32105
increased diameter of femur J:32105
increased long bone epiphyseal plate size J:32105
increased osteoclast cell number J:32105
increased width of hypertrophic chondrocyte zone J:32105
kyphoscoliosis J:32105
kyphosis J:32105
large femur head J:32105
lethality at weaning, incomplete penetrance J:32105
long femur J:32105
long humerus J:32105
long tail J:32105
respiratory distress J:32105
scoliosis J:32105
wavy tail J:32105
Fgfr3tm1Llm/Fgfr3+
involves: 129S2/SvPas 		abnormal cervical vertebrae morphology J:203653
abnormal endochondral bone ossification J:203653
abnormal epiphyseal plate morphology J:203653
abnormal head size J:203653
abnormal intramembranous bone ossification J:203653
abnormal long bone hypertrophic chondrocyte zone J:203653
decreased body length J:203653
decreased body weight J:203653
disproportionate dwarf J:203653
domed cranium J:203653
foramen magnum stenosis J:203653
prognathia J:203653
short femur J:203653
short lumbar vertebrae J:203653
short tail J:203653
short tibia J:203653
small snout J:203653
vertebral compression J:203653
Fgfr3tm1Llm/Fgfr3+
involves: 129S2/SvPas * C57BL/6J 		abnormal cochlea morphology J:147208
abnormal cochlear outer hair cell morphology J:147208
abnormal Deiters cell morphology J:147208
abnormal epiphyseal plate morphology J:147208
abnormal foramen magnum morphology J:147208
abnormal incus morphology J:147208
abnormal malleus morphology J:147208
abnormal middle ear ossicle morphology J:147208
abnormal organ of Corti morphology J:147208
abnormal skeleton morphology J:147208
abnormal stapes morphology J:147208
abnormal temporal bone morphology J:147208
bowed fibula J:147208
bowed radius J:147208
bowed tibia J:147208
bowed ulna J:147208
deafness J:147208
decreased body length J:147208
decreased chondrocyte number J:147208
decreased cranium height J:147208
decreased length of long bones J:147208
domed cranium J:147208
increased or absent threshold for auditory brainstem response J:147208
megacephaly J:147208
midface hypoplasia J:147208
premature death J:147208
prognathia J:147208
short basicranium J:147208
short femur J:147208
short ribs J:147208
small caudal vertebrae J:147208
Fgfr3tm1Schl/Fgfr3tm1Schl
involves: 129S1/Sv * CD-1 * FVB/N 		normal skeleton phenotype J:142946
Fgfr3tm1Wei/Fgfr3tm1Wei
involves: 129S1/Sv * 129X1/SvJ * MF1 		abnormal long bone morphology J:54829
bowed femur J:54829
increased long bone epiphyseal plate size J:54829
kinked tail J:54829
kyphosis J:54829
long femur J:54829
long tail J:54829
Fgfr3tm2Cxd/Fgfr3tm2Cxd
involves: 129S6/SvEvTac * NIH Black Swiss 		no abnormal phenotype detected J:52438
Fgfr3tm2Llm/Fgfr3+
Tg(Col2a1-cre)1Bhr/?
involves: 129S2/SvPas * C57BL/6 * SJL 		abnormal axial skeleton morphology J:183772
abnormal bone mineralization J:183772
abnormal bone structure J:183772
abnormal craniofacial bone morphology J:183772
abnormal long bone epiphyseal ossification zone morphology J:183772
abnormal long bone epiphyseal plate morphology J:183772
abnormal long bone epiphyseal plate proliferative zone J:183772
abnormal long bone epiphysis morphology J:183772
abnormal long bone morphology J:183772
abnormal skeleton development J:183772
abnormal thoracic cage morphology J:183772
abnormal trabecular bone morphology J:183772
decreased body size J:183772
decreased length of long bones J:183772
decreased width of hypertrophic chondrocyte zone J:183772
delayed bone ossification J:183772
domed cranium J:183772
increased osteoclast cell number J:183772
short ribs J:183772
Fgfr3tm2Llm/Fgfr3+
Tg(CMV-cre)1Ipc/?
involves: 129S2/SvPas * C57BL/6 * SJL 		abnormal axial skeleton morphology J:183772
abnormal bone mineralization J:183772
abnormal bone structure J:183772
abnormal craniofacial bone morphology J:183772
abnormal long bone epiphyseal ossification zone morphology J:183772
abnormal long bone epiphysis morphology J:183772
abnormal long bone morphology J:183772
abnormal skeleton development J:183772
abnormal thoracic cage morphology J:183772
abnormal trabecular bone morphology J:183772
decreased body size J:183772
decreased length of long bones J:183772
domed cranium J:183772
increased osteoclast cell number J:183772
short ribs J:183772
Fgfr3tm2Llm/Fgfr3+
Tg(Col1a1-cre)1Kry/0
involves: 129S2/SvPas * C57BL/6 * FVB 		normal skeleton phenotype J:183772
Fgfr3tm2Schl/Fgfr3tm2Schl
involves: 129S1/Sv * CD-1 * FVB/N 		abnormal axial skeleton morphology J:142946
abnormal bone structure J:142946
abnormal long bone epiphyseal plate morphology J:142946
abnormal long bone epiphyseal plate proliferative zone J:142946
abnormal long bone morphology J:142946
abnormal tail morphology J:142946
abnormal trabecular bone morphology J:142946
decreased bone mineral density J:142946
decreased compact bone thickness J:142946
increased width of hypertrophic chondrocyte zone J:142946
kinked tail J:142946
kyphosis J:142946
long femur J:142946
long humerus J:142946
long limbs J:142946
long tail J:142946
long tibia J:142946
long ulna J:142946
Fgfr3tm2Wei/Fgfr3+
involves: 129S1/Sv * 129X1/SvJ * MF1 		abnormal cranium morphology J:54829
abnormal foramen magnum morphology J:54829
abnormal long bone epiphyseal plate proliferative zone J:54829
abnormal maxilla morphology J:54829
abnormal parietal bone morphology J:54829
decreased long bone epiphyseal plate size J:54829
decreased width of hypertrophic chondrocyte zone J:54829
disorganized long bone epiphyseal plate J:54829
disproportionate dwarf J:54829
kyphosis J:54829
long incisors J:54829
malocclusion J:54829
misaligned incisors J:54829
round head J:54829
short frontal bone J:54829
short nasal bone J:54829
short tibia J:54829
Fgfr3tm3.1Cxd/Fgfr3+
involves: 129S6/SvEvTac 		abnormal cranium morphology J:69849
abnormal long bone epiphyseal plate morphology J:69849
abnormal synchondrosis J:69849
decreased cranium height J:69849
disproportionate dwarf J:69849
domed cranium J:69849
increased cranium width J:69849
megacephaly J:69849
short tail J:69849
Fgfr3tm3.1Cxd/Fgfr3tm3.1Cxd
involves: 129S6/SvEvTac 		abnormal bone ossification J:69849
abnormal cranium morphology J:69849
abnormal long bone epiphyseal plate morphology J:69849
abnormal long bone epiphyseal plate proliferative zone J:69849
abnormal long bone metaphysis morphology J:69849
abnormal long bone morphology J:69849
abnormal osteoclast physiology J:69849
abnormal trabecular bone morphology J:69849
decreased bone mineral density J:69849
decreased chondrocyte proliferation J:69849
decreased cranium height J:69849
decreased width of hypertrophic chondrocyte zone J:69849
delayed bone ossification J:69849
delayed endochondral bone ossification J:69849
disorganized long bone epiphyseal plate J:69849
disproportionate dwarf J:69849
domed cranium J:69849
enhanced osteoblast differentiation J:69849
increased cranium width J:69849
megacephaly J:69849
premature cranial synchondrosis closure J:69849
short basicranium J:69849
short femur J:69849
short humerus J:69849
short tail J:69849
small presphenoid bone J:69849
small vertebrae J:69849
Fgfr3tm3.1Llm/Fgfr3+
involves: C57BL/6N 		abnormal annulus fibrosus morphology J:338859
abnormal chondrocyte differentiation J:338859
abnormal compact bone lamellar structure J:338859
abnormal compact bone morphology J:338859
abnormal cranium morphology J:338859
abnormal endochondral bone ossification J:338859
abnormal foramen magnum morphology J:338859
abnormal long bone epiphyseal ossification zone morphology J:338859
abnormal skeleton morphology J:338859
abnormal trabecular bone morphology J:338859
abnormal vertebrae morphology J:338859
abnormal vertebral body morphology J:338859
decreased body length J:338859
decreased body size J:338859
decreased body weight J:338859
decreased bone mineral density of vertebrae J:338859
decreased bone stiffness J:338859
decreased bone strength J:338859
decreased bone trabecula number J:338859
decreased bone volume J:338859
decreased cranium length J:338859
decreased energy dissipated prior to femur fracture J:338859
decreased femur maximal load J:338859
decreased femur yield load J:338859
decreased length of long bones J:338859
decreased trabecular bone thickness J:338859
decreased vertebra maximal load J:338859
decreased vertebra stiffness J:338859
decreased width of hypertrophic chondrocyte zone J:338859
disorganized long bone epiphyseal plate J:338859
domed cranium J:338859
fragile skeleton J:338859
increased bone trabecular spacing J:338859
increased compact bone thickness J:338859
increased compact bone volume J:338859
increased cranium width J:338859
premature cranial synchondrosis closure J:338859
premature sphenooccipital synchondrosis closure J:338859
prognathia J:338859
short basicranium J:338859
short femur J:338859
short tibia J:338859
short vertebral body J:338859
Fgfr3tm3Cxd/Fgfr3tm3Cxd
involves: 129S6/SvEvTac 		abnormal behavior J:69849
abnormal breathing pattern J:69849
abnormal postnatal growth/weight/body size J:69849
abnormal skeleton morphology J:69849
lethality at weaning, complete penetrance J:69849
Fgfr3tm4.1Cxd/Fgfr3+
involves: 129S6/SvEvTac 		abnormal spine curvature J:70061
bowed tibia J:70061
bowed ulna J:70061
increased diameter of long bones J:70061
perinatal lethality, complete penetrance J:70061
round head J:70061
short limbs J:70061
Fgfr3tm4.1Cxd/Fgfr3+
involves: 129S6/SvEvTac * NIH Black Swiss 		abnormal bone ossification J:63198
abnormal chondrocyte differentiation J:63198
abnormal costal cartilage morphology J:63198
abnormal long bone diaphysis morphology J:63198
abnormal long bone epiphyseal plate morphology J:63198
abnormal long bone epiphyseal plate proliferative zone J:63198
abnormal long bone hypertrophic chondrocyte zone J:63198
abnormal long bone morphology J:63198
abnormal osteoblast physiology J:63198
abnormal spine curvature J:63198
abnormal thoracic cage shape J:63198
abnormal ulna morphology J:63198
bowed ulna J:63198
decreased length of long bones J:63198
failure of sternum ossification J:63198
impaired lung alveolus development J:63198
increased chondrocyte proliferation J:63198
increased diameter of long bones J:63198
increased fibroblast proliferation J:63198
normal mortality/aging J:70061
neonatal lethality, complete penetrance J:63198
round head J:63198
short femur J:63198
short humerus J:63198
short limbs J:63198
short tibia J:63198
short ulna J:63198
small thoracic cage J:63198
wide sternum J:63198
Fgfr3tm4Cxd/Fgfr3+
Tg(Col2a1-cre)1Bhr/0
involves: 129S6/SvEvTac * C57BL/6 * NIH Black Swiss * SJL 		abnormal skeleton morphology J:63198
impaired lung alveolus development J:63198
neonatal lethality, incomplete penetrance J:63198
Fgfr3tm4Cxd/Fgfr3+
Tg(Upk2-cre)6Xrw/0
involves: 129S6/SvEvTac * FVB/N 		normal neoplasm J:174242
Fgfr3tm5.1Cxd/Fgfr3+
involves: 129S6/SvEvTac 		abnormal chondrocyte differentiation J:67780
abnormal chondrocyte morphology J:67780
abnormal cranium morphology J:67780
abnormal long bone epiphyseal plate morphology J:67780
abnormal long bone epiphyseal plate proliferative zone J:67780
abnormal long bone hypertrophic chondrocyte zone J:67780
bowed fibula J:67780
bowed tibia J:67780
decreased cranium height J:67780
decreased length of long bones J:67780
decreased long bone epiphyseal plate size J:67780
decreased width of hypertrophic chondrocyte zone J:67780
disorganized long bone epiphyseal plate J:67780
disproportionate dwarf J:67780
domed cranium J:67780
increased cranium width J:67780
long incisors J:67780
male infertility J:67780
premature cranial synchondrosis closure J:67780
premature death J:67780
premature endochondral bone ossification J:67780
reduced female fertility J:67780
short basicranium J:67780
short femur J:67780
short tail J:67780
Fgfr3tm5Cxd/Fgfr3tm5Cxd
involves: 129S6/SvEvTac 		abnormal behavior J:67780
abnormal breathing pattern J:67780
abnormal postnatal growth/weight/body size J:67780
abnormal skeleton morphology J:67780
lethality at weaning, complete penetrance J:67780
Fgfr3tm6.2Cxd/Fgfr3tm6.2Cxd
involves: 129S6/SvEvTac * FVB/N 		decreased bone mineral density J:161199
long femur J:161199
Fgfr3tm6Cxd/Fgfr3tm6Cxd
involves: 129S6/SvEvTac 		abnormal chondrocyte physiology J:161199
kinked tail J:161199
Tg(Col2a1-Fgfr3/GH)ADor/Tg(Col2a1-Fgfr3/GH)ADor
FVB/N-Tg(Col2a1-Fgfr3/GH)ADor 		proportional dwarf J:50292
Tg(Col2a1-Fgfr3/GH)BDor/0
FVB/N-Tg(Col2a1-Fgfr3/GH)BDor 		abnormal appendicular skeleton morphology J:50292
abnormal chondrocyte physiology J:50292
abnormal craniofacial bone morphology J:50292
abnormal limb bone morphology J:50292
abnormal long bone epiphyseal ossification zone morphology J:50292
abnormal long bone epiphyseal plate proliferative zone J:50292
abnormal osteoclast differentiation J:50292
abnormal perichondrium morphology J:50292
abnormal vertebrae development J:50292
abnormal vertebrae morphology J:50292
absent vertebral spinous process J:50292
axial skeleton hypoplasia J:50292
decreased length of long bones J:50292
decreased long bone epiphyseal plate size J:50292
decreased width of hypertrophic chondrocyte zone J:50292
delayed endochondral bone ossification J:50292
domed cranium J:50292
kyphosis J:50292
proportional dwarf J:50292
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
04/16/2024
MGI 6.23 		The Jackson Laboratory