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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID 		Nefh
neurofilament, heavy polypeptide
MGI:97309
11 phenotypes from 5 alleles in 5 genetic backgrounds
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Allelic Composition
Genetic Background		 Annotated Term Reference
Nefhtm1.1(KOMP)Vlcg/Nefhtm1.1(KOMP)Vlcg
C57BL/6N-Nefhtm1.1(KOMP)Vlcg/J 		decreased mean corpuscular hemoglobin concentration J:211773
increased circulating alanine transaminase level J:211773
Nefhtm1Dwc/Nefhtm1Dwc
involves: 129S1/Sv * 129X1/SvJ * C57BL/6J 		abnormal axon extension J:77654
abnormal motor neuron morphology J:77654
abnormal sensory neuron morphology J:77654
Nefhtm1Jpj/Nefhtm1Jpj
involves: 129S1/Sv * 129X1/SvJ * C57BL/6 		abnormal axon morphology J:56931
abnormal ventral spinal root morphology J:56931
Nefhtm1Ral/Nefh+
either: (involves: 129S1/Sv * 129X1/SvJ * C57BL/6) or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * Swiss Webster) 		abnormal axon morphology J:78119
Nefhtm1Ral/Nefhtm1Ral
either: (involves: 129S1/Sv * 129X1/SvJ * C57BL/6) or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * Swiss Webster) 		abnormal axon morphology J:78119
normal nervous system phenotype J:78119
Nefhtm1Ral/Nefhtm1Ral
involves: 129S1/Sv * 129X1/SvJ 		abnormal axon morphology J:77656
axon degeneration J:77656
Nefhtm2Dwc/Nefhtm2Dwc
involves: 129S1/Sv * 129X1/SvJ 		abnormal neuron differentiation J:87156
normal behavior/neurological phenotype J:87156
normal nervous system phenotype J:87156
Nefhtm2Dwc/Nefhtm2Dwc
involves: 129S1/Sv * 129X1/SvJ * C57BL/6J 		abnormal axon morphology J:78725
normal nervous system phenotype J:78725
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
11/12/2024
MGI 6.24 		The Jackson Laboratory