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Summary Expression Phenotypes Gene Literature (3) GO Terms (11) Nucleotides (300) Proteins (41) Interactants (80) Wiki
XB-GENEPAGE-5741890

rmnd5a     required for meiotic nuclear division 5 homolog A

Anatomical Phenotypes
Phenotypes manually curated with terms from the Xenopus phenotype ontology covering anatomical, gene ontology, and neurobehavioral phenotypes.
decreased size of the forebrain (4 sources), abnormal eye (2 sources), abnormal Meckel's cartilage (1 source), abnormal anterior-posterior axis, curved lateral (1 source), abnormal brain (1 source), abnormal branchial basket (1 source), abnormal ceratohyal morphology (1 source), abnormal eye primordium (1 source), abnormal forebrain (1 source), abnormal head morphology (1 source), abnormal left side (1 source), abnormal neural tube (1 source), abnormal neural tube morphology (1 source), abnormal optic vesicle (1 source), abnormal palatoquadrate (1 source), decreased size of the Meckel's cartilage (1 source), decreased size of the ceratohyal (1 source), decreased size of the eye (1 source), decreased size of the head region (1 source), decreased size of the optic vesicle (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.
Manual annotations: rmnd5a manipulated (12 sources)
Diseases
Diseases from the human disease ontology (DO) manually associated with phenotypes from disease models. Sources are grouped by anatomical (AP) and expression (EP) phenotypes.
microphthalmia (1AP source, 1 EP source), neural tube defect (1AP source, 1 EP source)
Experiments (Reagents)
These are short form descriptions of experiments using reagents targeting the gene of interest.
Xla Wt + rmnd5a MO (13 sources), Xla Wt + rmnd5a MO (8 sources)