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XB-GENEPAGE-1001231
p3h2 prolyl 3-hydroxylase 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.
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| Computed annotations: p3h2 assayed (5 sources) |
| Monarch Ortholog Phenotypes
These phenotypes are associated with this gene with a has phenotype relation via Monarch.
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| Human (5 sources): Cataract, High myopia, Lens subluxation, Peripheral vitreoretinal degeneration, Retinal detachment |
| Mouse (7 sources): abnormal circulating potassium level, abnormal snout morphology, abnormal thrombosis, embryonic lethality during organogenesis, complete penetrance, embryonic lethality, incomplete penetrance, prolonged RR interval, skeleton phenotype |
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View all ortholog results at Monarch |