mocs2 Phenotypes

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Phenotypes

Gene Literature (1)

Nucleotides (126)

Interactants (60)

XB-GENEPAGE-964467

Gene Symbol: mocs2 Gene Name: molybdenum cofactor synthesis 2

Expression Phenotypes Gene expression phenotype annotations where the gene of interest has been disrupted (manipulated) or is the gene assayed (assayed). Computed annotations are derived from differential expression analysis from Xenbase processed GEO data with the criteria of a TPM >= 1, FDR <= 0.05 and an absolute LogFC >= 2.
Computed annotations: mocs2 assayed (4 sources)

Monarch Ortholog Phenotypes These phenotypes are associated with this gene with a has phenotype relation via Monarch.
Human (31 sources): Axonal loss, Cerebral atrophy, Ectopia lentis, Feeding difficulties, Frontal bossing, Full cheeks, Gliosis, Growth delay, Hypertelorism, Hypoplasia of the corpus callosum, Hypouricemia, Increased urinary hypoxanthine level, Increased urinary taurine, Lens luxation, Long face, Long philtrum, Macrocephaly, Microcephaly, Molybdenum cofactor deficiency, Myoclonic spasms, Nystagmus, Opisthotonus, Peripheral demyelination, Seizure, Short nose, Spastic tetraplegia, Spasticity, Thick vermilion border, Ventriculomegaly, Xanthine nephrolithiasis, Xanthinuria [+]
Mouse (18 sources): abnormal blood homeostasis, abnormal kidney collecting duct morphology, abnormal kidney pelvis morphology, abnormal vibrissa morphology, curly vibrissae, cystolithiasis, decreased body length, decreased body size, erythrocyturia, flaky skin, increased circulating creatinine level, increased neuron apoptosis, increased startle reflex, postnatal lethality, complete penetrance, preweaning lethality, complete penetrance, slow postnatal weight gain, urinary bladder obstruction, weakness [+]
View all ortholog results at Monarch