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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Scyl1
SCY1-like 1 (S. cerevisiae)
MGI:1931787
15 phenotypes from multigenic genotypes
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Allelic Composition
Genetic Background
Annotated Term Reference
Scyl1tm1.1Spel/Scyl1tm1.1Spel
Scyl3tm1.1Spel/Scyl3tm1.1Spel
involves: 129S6/SvEvTac * C57BL/6J
abnormal myelination J:262629
abnormal sciatic nerve morphology J:262629
decreased body height J:262629
decreased body size J:262629
decreased grip strength J:262629
decreased motor neuron number J:262629
decreased skeletal muscle fiber diameter J:262629
gliosis J:262629
motor neuron degeneration J:262629
paralysis J:262629
postnatal growth retardation J:262629
Scyl1tm1Spel/Scyl1tm1Spel
Tg(Ckmm-cre)5Khn/0
involves: 129S4/SvJae * 129S6/SvEvTac * C57BL/6J * FVB/N
normal behavior/neurological phenotype J:192445
normal muscle phenotype J:192445
normal nervous system phenotype J:192445

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
09/15/2026
MGI 6.29
The Jackson Laboratory