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XB-GENEPAGE-942747
sdr16c5 short chain dehydrogenase/reductase family 16C member 5
Anatomical Phenotypes
Phenotypes manually curated with terms from the Xenopus phenotype ontology
covering anatomical, gene ontology, and neurobehavioral phenotypes.
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| decreased length of anterior-posterior axis (5 sources), abnormally anteriorly mislocalised eye (4 sources), abnormally incomplete structure of head (4 sources), absent eye (4 sources), fused eyes (4 sources), abnormal NAD-retinol dehydrogenase activity (1 source), abnormal bending of tail (1 source), abnormal development of somite (1 source), abnormal development of tail (1 source), abnormal neural tube closure (1 source), abnormally irregular spatial pattern of somite (1 source), abnormally posterioralized embryo (1 source), decreased size of the eye (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: sdr16c5 manipulated (6 sources) |
| Experiments (Reagents)
These are short form descriptions of experiments using reagents targeting
the gene of interest.
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| Xla Wt + sdr16c5 MO (6 sources), Xla Wt + sdr16c5 MO (2 sources), Xla Wt + aldh1a2 + sdr16c5 + retinol (1 source), Xla Wt + aldh1a2 + sdr16c5 + retinol (1 source), Xla Wt + sdr16c5 (1 source), Xla Wt + sdr16c5 + retinol (1 source), Xla Wt + sdr16c5 + retinol (1 source), Xla Wt + sdr16c5 + retinol (1 source) |