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Symbol Name ID |
Scyl2
SCY1-like 2 (S. cerevisiae) MGI:1289172 |
| Darker colors indicate more annotations |
| Human Phenotypes | Microcephaly |
Spasticity |
Frontal cortical atrophy |
Parietal cortical atrophy |
Agenesis of corpus callosum |
Areflexia |
Global developmental delay |
Seizure |
| Disease(s) Associated with SCYL2 | ||||||||
| arthrogryposis multiplex congenita-4 |
| Mouse Phenotypes | increased neuron apoptosis |
microgliosis |
decreased brain size |
decreased dentate gyrus size |
decreased hippocampus pyramidal cell number |
hippocampal neuron degeneration |
small hippocampus |
astrocytosis |
abnormal excitatory postsynaptic potential |
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| Availability | Mouse Genotype | |||||||||
| Scyl2tm1.1Spel/Scyl2tm1.1Spel Tg(Nes-cre)1Kln/0 (conditional) |
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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 05/14/2024 MGI 6.23 |
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