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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID 		Cfap276
cilia and flagella associated protein 276
MGI:1922754
28 phenotypes from 3 alleles in 3 genetic backgrounds
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Allelic Composition
Genetic Background		 Annotated Term Reference
Cfap276em1Fuxi/Cfap276+
C57BL/6J-Cfap276em1Fuxi 		abnormal action potential J:283448
abnormal gait J:283448
abnormal internode morphology J:283448
abnormal myelin sheath morphology J:283448
abnormal sciatic nerve morphology J:283448
axon degeneration J:283448
decreased body weight J:283448
decreased grip strength J:283448
demyelination J:283448
impaired coordination J:283448
increased myelin sheath thickness J:283448
limb grasping J:283448
paraparesis J:283448
short stride length J:283448
skeletal muscle atrophy J:283448
Cfap276em1Fuxi/Cfap276em1Fuxi
C57BL/6J-Cfap276em1Fuxi 		abnormal gait J:283448
abnormal internode morphology J:283448
abnormal myelin sheath morphology J:283448
abnormal sciatic nerve morphology J:283448
axon degeneration J:283448
decreased body weight J:283448
decreased grip strength J:283448
demyelination J:283448
impaired coordination J:283448
increased myelin sheath thickness J:283448
limb grasping J:283448
paraparesis J:283448
short stride length J:283448
skeletal muscle atrophy J:283448
Cfap276em1Osb/Cfap276em1Osb
involves: C57BL/6NJcl * DBA/2NJcl 		reproductive system phenotype J:348435
Cfap276em2.1Fuxi/Cfap276+
involves: C57BL/6J 		abnormal action potential J:295996
abnormal internode morphology J:295996
abnormal myelin sheath morphology J:295996
abnormal physical strength J:295996
decreased grip strength J:295996
decreased motor neuron number J:295996
decreased nerve conduction velocity J:295996
demyelination J:295996
hyporesponsive to tactile stimuli J:295996
impaired coordination J:295996
increased myelin sheath thickness J:295996
limb grasping J:295996
short stride length J:295996
skeletal muscle fiber atrophy J:295996
Cfap276em2.1Fuxi/Cfap276em2.1Fuxi
involves: C57BL/6J 		abnormal action potential J:295996
abnormal embryo development J:295996
abnormal gait J:295996
abnormal internode morphology J:295996
abnormal motor capabilities/coordination/movement J:295996
abnormal physical strength J:295996
abnormal placenta morphology J:295996
abnormal sciatic nerve morphology J:295996
axon degeneration J:295996
decreased embryo size J:295996
decreased grip strength J:295996
decreased motor neuron number J:295996
decreased nerve conduction velocity J:295996
demyelination J:295996
embryonic lethality, incomplete penetrance J:295996
hyporesponsive to tactile stimuli J:295996
impaired coordination J:295996
impaired embryo implantation J:295996
increased myelin sheath thickness J:295996
limb grasping J:295996
muscular atrophy J:295996
short stride length J:295996
skeletal muscle fiber atrophy J:295996
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
11/19/2024
MGI 6.24 		The Jackson Laboratory