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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Idua
iduronidase, alpha-L
MGI:96418
113 phenotypes from 5 alleles in 7 genetic backgrounds
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Allelic Composition
Genetic Background
Annotated Term Reference
Iduaem1Btlr/Iduam1Btlr
C57BL/6J-Iduaem1Btlr/Iduam1Btlr/Btlr
decreased bone trabecular spacing J:309727
increased bone mineral density J:309727
increased bone trabecula number J:309727
increased trabecular bone volume J:309727
Iduam1Btlr/Iduam1Btlr
C57BL/6J-Iduam1Btlr/Btlr
increased bone mineral density J:309727
Iduatm1.1Kmke/Iduatm1.1Kmke
B6.129-Iduatm1.1Kmke
abnormal foam cell morphology J:155619
abnormal lysosome morphology J:155619
abnormal zygomatic bone morphology J:155619
broad snout J:155619
decreased percent body fat/body weight J:155619
increased bone mineral density of femur J:155619
increased diameter of femur J:155619
increased urine glycosaminoglycan level J:155619
premature death J:155619
short femur J:155619
Iduatm1Clk/Iduatm1Clk
B6.129-Iduatm1Clk/J
abnormal learning/memory/conditioning J:130215
abnormal long-term spatial reference memory J:130215
abnormal response to novel object J:130215
abnormal spatial learning J:130215
decreased locomotor activity J:130215
decreased startle reflex J:130215
decreased survivor rate J:130215
increased anxiety-related response J:130215
increased body weight J:130215
increased urine glycosaminoglycan level J:130215
Iduatm1Clk/Iduatm1Clk
involves: 129S1/Sv * 129X1/SvJ
abnormal axial skeleton morphology J:47999
abnormal chondrocyte morphology J:39522
abnormal digit morphology J:39522
abnormal eye morphology J:47999
abnormal gait J:47999
abnormal limb morphology J:47999
abnormal long bone diaphysis morphology J:47999
abnormal long bone hypertrophic chondrocyte zone J:47999
abnormal long bone morphology J:47999
abnormal neuron morphology J:39522, J:47999
abnormal Purkinje cell morphology J:39522
abnormal rib morphology J:39522, J:47999
abnormal tibia morphology J:47999
abnormal vertebrae morphology J:47999
broad face J:39522
congestive heart failure J:47999
decreased locomotor activity J:47999
disheveled coat J:47999
hip dislocation J:47999
increased autopod size J:39522
increased cranium width J:47999
increased osteoblast cell number J:47999
increased urine glycosaminoglycan level J:39522
kyphosis J:47999
lysosomal protein accumulation J:39522
ocular hypertelorism J:47999
pale liver J:39522
postnatal growth retardation J:47999
premature death J:47999
prominent nasal bridge J:47999
Purkinje cell degeneration J:47999
short snout J:47999
sparse hair J:47999
Iduatm1Clk/Iduatm1Clk
involves: 129S1/Sv * 129X1/SvJ * C57BL/6
abnormal circulating enzyme level J:138341
Iduatm1Efn/Iduatm1Efn
involves: C57BL/6
abnormal aorta elastic fiber morphology J:101932
abnormal aorta smooth muscle morphology J:101932
abnormal aortic valve morphology J:101932
abnormal avoidance learning behavior J:107064
abnormal basicranium morphology J:117424
abnormal cardiac muscle relaxation J:101932
abnormal cerebellar cortex morphology J:81974
abnormal cervical vertebrae morphology J:117424
abnormal circadian behavior J:101932
abnormal circadian regulation of heart rate J:101932
abnormal circadian temperature homeostasis J:101932
abnormal craniofacial morphology J:117424
abnormal endocardium morphology J:101932
abnormal external auditory canal morphology J:117424
abnormal foramen magnum morphology J:117424
abnormal heart electrocardiography waveform feature J:101932
abnormal heart left ventricle outflow tract morphology J:101932
abnormal heart ventricle morphology J:101932
abnormal incisor morphology J:117424
abnormal inner ear morphology J:123676
abnormal lysosome morphology J:123676
abnormal mandibular condyloid process morphology J:117424
abnormal metabolism J:101932
abnormal microglial cell morphology J:81974
abnormal microglial cell physiology J:81974
abnormal mitral valve morphology J:101932
abnormal myocardial fiber morphology J:101932
abnormal myocardium layer morphology J:101932
abnormal QRS complex J:101932
abnormal tricuspid valve morphology J:101932
abnormal zygomatic arch morphology J:117424
aortic valve regurgitation J:101932
cochlear ganglion degeneration J:123676
cochlear hair cell degeneration J:123676
deafness J:123676
decreased body temperature J:101932
decreased cardiac output J:101932
decreased heart rate variability J:101932
decreased ventricle muscle contractility J:101932
decreased vertical activity J:107064
enlarged aortic valve J:101932
enlarged heart J:101932
enlarged mitral valve J:101932
enlarged tricuspid valve J:101932
increased collagen deposition in the muscles J:101932
increased heart left ventricle posterior wall thickness J:101932
increased heart left ventricle septal wall thickness J:101932
increased heart left ventricle wall thickness J:101932
increased heart weight J:101932
increased or absent threshold for auditory brainstem response J:123676
increased susceptibility to otitis media J:123676
increased systemic arterial systolic blood pressure J:101932
mitral valve regurgitation J:101932
organ of Corti degeneration J:123676
premature death J:101932
prolonged P wave J:101932
prolonged QRS complex duration J:101932
sensorineural hearing loss J:123676
spiral ligament degeneration J:123676
thick aortic valve cusps J:101932
thick interventricular septum J:101932

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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last database update
04/16/2024
MGI 6.23
The Jackson Laboratory