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XB-GENEPAGE-487370
snai2 snail family transcriptional repressor 2
Anatomical Phenotypes
Phenotypes manually curated with terms from the Xenopus phenotype ontology
covering anatomical, gene ontology, and neurobehavioral phenotypes.
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abnormal cell migration in neural crest (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: snai2 manipulated (5 sources), snai2 assayed (102 sources) |
Computed annotations: snai2 assayed (9 sources) |
Experiments (Reagents)
These are short form descriptions of experiments using reagents targeting
the gene of interest.
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Xla Wt + snai2 MO (2 sources), Xla Wt + hmga2 + snai2 (1 source), Xla Wt + snai2 (1 source), Xla Wt + dnsnai2 (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): Abnormality of calvarial morphology, Abnormality of the ear, Abnormality of the kidney, Abnormality of the pulmonary artery, Absent pigmentation of the ventral chest, Aganglionic megacolon, Ataxia, Congenital sensorineural hearing impairment, Hearing impairment, Heterochromia iridis, [+] |
Mouse (24 sources): abnormal T cell differentiation, abnormal cardiac epithelial to mesenchymal transition, abnormal fetal atrioventricular canal morphology, abnormal hematopoietic system morphology/development, circling, decreased atrioventricular cushion size, decreased body size, decreased forehead pigmentation, decreased hematocrit, decreased hemoglobin content, [+] |
View all ortholog results at Monarch |