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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Wld
wallerian degeneration
MGI:98952
12 phenotypes from multigenic genotypes
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Allelic Composition
Genetic Background
Annotated Term Reference
Cmtm5tm1d(KOMP)Wtsi/Cmtm5tm1d(KOMP)Wtsi
Wlds/+
B6(Cg)-Wlds Cmtm5tm1d(KOMP)Wtsi
abnormal axon morphology J:327261
Nmnat2Gt(EUCE0262a08)Hmgu/Nmnat2Gt(EUCE0262a08)Hmgu
Wlds/+
involves: 129P2/OlaHsd * C57BL/6J * C57BL/6Ola
normal behavior/neurological phenotype J:200901
normal muscle phenotype J:200901
neonatal lethality, complete penetrance J:200901
normal nervous system phenotype J:200901
normal renal/urinary system phenotype J:200901
Nmnat2Gt(EUCE0262a08)Hmgu/Nmnat2Gt(EUCE0262a08)Hmgu
Wlds/Wlds
involves: 129P2/OlaHsd * C57BL/6J * C57BL/6Ola
no abnormal phenotype detected J:200901
Tg(SOD1*G93A)1Gur/0
Wlds/+
involves: C57BL/6J * C57BL/6Ola * SJL/J
abnormal motor neuron innervation pattern J:105092
decreased motor neuron number J:105092
decreased sensory neuron number J:105092
premature death J:105092
slow Wallerian degeneration J:105092
Tg(SOD1*G93A)1Gur/0
Wlds/Wlds
involves: C57BL/6J * C57BL/6Ola * SJL/J
premature death J:105092

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
04/30/2024
MGI 6.23
The Jackson Laboratory