About Help FAQ

Symbol
Name
ID

Scyl2
SCY1-like 2 (S. cerevisiae)
MGI:1289172

Phenotype annotations related to behavior/neurological

Darker colors indicate more annotations

Human Phenotypes	Decreased fetal movement	Feeding difficulties in infancy
Disease(s) Associated with SCYL2	Decreased fetal movement	Feeding difficulties in infancy
arthrogryposis multiplex congenita-4

Mouse Phenotypes		abnormal behavior	absent gastric milk in neonates	abnormal depression-related behavior	limb grasping	tremors	decreased grip strength
Availability	Mouse Genotype	abnormal behavior	absent gastric milk in neonates	abnormal depression-related behavior	limb grasping	tremors	decreased grip strength
	Scyl2^tm1.2Spel/Scyl2^tm1.2Spel
	Scyl2^tm1.1Spel/Scyl2^tm1.1Spel Tg(Nes-cre)1Kln/0 (conditional)

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)
Citing These Resources Funding Information Warranty Disclaimer, Privacy Notice, Licensing, & Copyright Send questions and comments to User Support.	last database update 04/30/2024 MGI 6.23