Symbol Name ID |
Mocs2
molybdenum cofactor synthesis 2 MGI:1336894 |
Darker colors indicate more annotations |
Human Phenotypes | Microcephaly |
Spastic tetraplegia |
Opisthotonus |
Gliosis |
Peripheral demyelination |
Axonal loss |
Ventriculomegaly |
Thin corpus callosum |
Hypoplasia of the corpus callosum |
Cerebral atrophy |
Diffuse cerebral atrophy |
Myoclonic spasms |
Irritability |
Global developmental delay |
Seizure |
Bilateral tonic-clonic seizure |
Disease(s) Associated with MOCS2 | ||||||||||||||||
molybdenum cofactor deficiency type B |
Mouse Phenotypes | increased neuron apoptosis |
|
Availability | Mouse Genotype | |
Mocs2tm1(KOMP)Vlcg/Mocs2tm1(KOMP)Vlcg | ||
Mocs2tm1(KOMP)Vlcg/Mocs2+ |
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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