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XB-GENEPAGE-480637
chrd chordin, gene 1
Anatomical Phenotypes
Phenotypes manually curated with terms from the Xenopus phenotype ontology
covering anatomical, gene ontology, and neurobehavioral phenotypes.
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wholly ventralized embryo (3 sources), abnormally posterioralized embryo (1 source), abnormally ventralized embryo (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: chrd manipulated (6 sources), chrd assayed (76 sources) |
Computed annotations: chrd manipulated (1 source), chrd assayed (44 sources) |
Experiments (Reagents)
These are short form descriptions of experiments using reagents targeting
the gene of interest.
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Xla Wt + chrd.1 MO (3 sources), Xtr Wt + chrd.1 CRISPR (3 sources), Xtr Wt + rspo2 CRISPR + chrd.1 CRISPR (2 sources), Xla Wt + chrd MO + nog MO (1 source), Xla Wt + chrd MO + nog MO (1 source), Xla Wt + chrd.1 + animal cap explant (1 source) |
Monarch Ortholog Phenotypes
These phenotypes are associated with this gene with a has phenotype relation via Monarch.
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Mouse (78 sources): abnormal artery morphology, abnormal brachiocephalic trunk morphology, abnormal brain development, abnormal cardiovascular development, abnormal common carotid artery morphology, abnormal cranial ganglia morphology, abnormal ear development, abnormal ear position, abnormal embryonic tissue morphology, abnormal extraembryonic tissue morphology, [+] |