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XB-GENEPAGE-982218
slc39a14 solute carrier family 39 (zinc transporter), member 14
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.
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Computed annotations: slc39a14 assayed (1 source) |
Monarch Ortholog Phenotypes
These phenotypes are associated with this gene with a has phenotype relation via Monarch.
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Human (30 sources): Ankle clonus, Axial hypotonia, Babinski sign, Bradykinesia, Bulbar signs, Cerebellar atrophy, Cerebral atrophy, Developmental regression, Dyskinesia, Dystonia, [+] |
Mouse (34 sources): abnormal chondrocyte differentiation, abnormal gluconeogenesis, abnormal growth hormone level, abnormal liver zinc level, abnormal osteoblast physiology, craniofacial phenotype, decreased body size, decreased bone mineralization, decreased bone ossification, decreased bone stiffness, [+] |
View all ortholog results at Monarch |