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XB-GENEPAGE-966777
jmjd6 jumonji domain containing 6
Anatomical Phenotypes
Phenotypes manually curated with terms from the Xenopus phenotype ontology
covering anatomical, gene ontology, and neurobehavioral phenotypes.
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| abnormal incomplete closing of the neural tube (1 source), abnormally incomplete structure of head (1 source), decreased length of anterior-posterior axis (1 source), decreased size of the head (1 source) |
| 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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| Manual annotations: jmjd6 manipulated (5 sources) |
| Computed annotations: jmjd6 assayed (1 source) |
| Experiments (Reagents)
These are short form descriptions of experiments using reagents targeting
the gene of interest.
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| Xla Wt + jmjd6 MO (3 sources), Xla Wt + jmjd6 MO + tcf7l1 MO (1 source), Xla Wt + jmjd6 MO + tcf7l1 MO (1 source), Xla Wt + tcf7l1 + jmjd6 MO (1 source) |
| Monarch Ortholog Phenotypes
These phenotypes are associated with this gene with a has phenotype relation via Monarch.
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| Mouse (17 sources): abnormal erythropoiesis, abnormal kidney development, abnormal macrophage activation involved in immune response, abnormal retina blood vessel morphology, abnormal retina vasculature morphology, abnormal sinus arrhythmia, cellular phenotype, decreased circulating iron level, fetal growth retardation, increased startle reflex, [+] |