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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Fign
fidgetin
MGI:1890647
46 phenotypes from 2 alleles in 5 genetic backgrounds
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Allelic Composition
Genetic Background
Annotated Term Reference
Fignfi/Fignfi
involves: 129P2/OlaHsd * 129S1/SvImJ * C57BL/6
cleft secondary palate J:116474
Fignfi/Fignfi
involves: 129S1/SvImJ * C57BL/6
cleft secondary palate J:116474
Fignfi/Fignfi
mixed
abnormal acetabular fossa morphology J:13048
abnormal cell cycle J:5736
abnormal cerebellar lobule formation J:13048
abnormal cornea morphology J:13048
abnormal craniofacial bone morphology J:13048
abnormal locomotor coordination J:13035
abnormal mandible morphology J:13048
abnormal maternal nurturing J:13035
abnormal membranous labyrinth morphology J:13048
abnormal otic capsule morphology J:13048
abnormal pelvic girdle bone morphology J:13048
abnormal pterygoid process morphology J:13048
abnormal retinal development J:5736
abnormal retinal progenitor cell morphology J:5736
absent lacrimal glands J:13048
absent lateral semicircular canal J:13048
absent mandibular canal J:13048
absent mandibular foramen J:13048
absent mental foramen J:13048
absent semicircular canals J:13048
absent subarcuate fossa J:13048
bidirectional circling J:13035
conjunctivitis J:13035
corneal opacity J:13035
corneal vascularization J:13035
deafness J:13035, J:13048
decreased body weight J:13035
eye inflammation J:13035
fused tarsal bones J:13048
Harderian gland hypertrophy J:13048
head shaking J:13035
normal hearing/vestibular/ear phenotype J:13048
hip dislocation J:13048
impaired coordination J:13035
increased startle reflex J:13035
increased susceptibility to age-related hearing loss J:13035
Meibomian gland hypertrophy J:13048
microphthalmia J:13048
polydactyly J:13035
postnatal growth retardation J:13035
reduced fertility J:13035
small lens J:13048
Figntm1Frk/Fignfi
involves: 129S1/Sv * 129X1SvJ * C57BL/6J
abnormal semicircular canal morphology J:64964
absent semicircular canals J:64964
head shaking J:64964
microphthalmia J:64964
Figntm1Frk/Figntm1Frk
B6.129-Figntm1Frk/Frk
head shaking J:64964
microphthalmia J:64964
postnatal lethality, incomplete penetrance J:64964
prenatal lethality, incomplete penetrance J:64964

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
11/12/2019
MGI 6.14
The Jackson Laboratory