Symbol Name ID |
Mocs2
molybdenum cofactor synthesis 2 MGI:1336894 |
Darker colors indicate more annotations |
Human Phenotypes | Hypertonia |
Spastic tetraplegia |
Opisthotonus |
Hypotonia |
Disease(s) Associated with MOCS2 | ||||
molybdenum cofactor deficiency type B |
Mouse Phenotypes | muscle weakness |
|
Availability | Mouse Genotype | |
Mocs2tm1(KOMP)Vlcg/Mocs2tm1(KOMP)Vlcg |
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 04/09/2024 MGI 6.23 |
|
|