Nefh Phenotype Annotations - Multigenic Genotypes

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Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Nefh
neurofilament, heavy polypeptide
MGI:97309

10 phenotypes from multigenic genotypes

Allelic Composition Genetic Background	Annotated Term	Reference
Nefh^tm1Dwc/Nefh^tm1Dwc Nefm^tm1Jpj/Nefm^tm1Jpj involves: 129S1/Sv * 129X1/SvJ	abnormal axonal transport	J:112938
Nefh^tm1Jpj/Nefh^tm1Jpj Nefm^tm1Jpj/Nefm^tm1Jpj involves: 129S1/Sv * 129X1/SvJ * C57BL/6	abnormal axon morphology	J:56931
	abnormal neuron morphology	J:56931
	abnormal ventral spinal root morphology	J:56931
	decreased motor neuron number	J:56931
Nefh^tm1Ral/Nefh^tm1Ral Nefm^tm1Ral/Nefm^tm1Ral involves: 129S1/Sv * 129X1/SvJ	abnormal axon morphology	J:77656
	axon degeneration	J:77656
	hindlimb paralysis	J:77656
Nefh^tm2Dwc/Nefh^tm2Dwc Nefm^tm1Mvr/Nefm^tm1Mvr involves: 129S1/Sv * 129X1/SvJ	abnormal action potential	J:87156
	abnormal axon morphology	J:87156
	normal behavior/neurological phenotype	J:87156
	normal nervous system phenotype	J:87156

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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