Symbol Name ID |
Scyl2
SCY1-like 2 (S. cerevisiae) MGI:1289172 |
Darker colors indicate more annotations |
Human Phenotypes | Decreased fetal movement |
Feeding difficulties in infancy |
Disease(s) Associated with SCYL2 | ||
arthrogryposis multiplex congenita-4 |
Mouse Phenotypes | abnormal behavior |
absent gastric milk in neonates |
abnormal depression-related behavior |
limb grasping |
tremors |
decreased grip strength |
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Availability | Mouse Genotype | ||||||
Scyl2tm1.2Spel/Scyl2tm1.2Spel | |||||||
Scyl2tm1.1Spel/Scyl2tm1.1Spel Tg(Nes-cre)1Kln/0 (conditional) |
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 08/02/2024 MGI 6.24 |
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