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Symbol
Name
ID

Mocs2
molybdenum cofactor synthesis 2
MGI:1336894

Phenotype annotations related to nervous system

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	increased neuron apoptosis
	Mocs2^{tm1(KOMP)Vlcg}/Mocs2^{tm1(KOMP)Vlcg}
	Mocs2^{tm1(KOMP)Vlcg}/Mocs2⁺

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)
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