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Summary Expression Phenotypes Gene Literature (9) GO Terms (29) Nucleotides (232) Proteins (66) Interactants (236) Wiki
XB-GENEPAGE-950754

chd2     chromodomain helicase DNA binding protein 2

Anatomical Phenotypes
Phenotypes manually curated with terms from the Xenopus phenotype ontology covering anatomical, gene ontology, and neurobehavioral phenotypes.
abnormal cell migration in neural crest (1 source), abnormally localised neural progenitor cell (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: chd2 manipulated (2 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.
autism spectrum disorder (1AP source, 1 EP source)
Experiments (Reagents)
These are short form descriptions of experiments using reagents targeting the gene of interest.
Xtr Wt + chd2 CRISPR (1 source), Xtr Wt + chd2 MO (1 source)
Monarch Ortholog Phenotypes
These phenotypes are associated with this gene with a has phenotype relation via Monarch.
Human (55 sources): Abnormal brain FDG positron emission tomography, Abnormal brainstem morphology, Abnormality of the dentition, Abnormal periventricular white matter morphology, Aggressive behavior, Ataxia, Atonic seizure, Atypical absence seizure, Atypical behavior, Autistic behavior, [+]
Mouse (45 sources): abnormal blood cell morphology/development, abnormal body length, abnormal bone mineralization, abnormal erythropoiesis, abnormal grip strength, abnormal kidney morphology, abnormal prepulse inhibition, cardiac fibrosis, cortical renal glomerulopathies, decreased birth body size, [+]

View all ortholog results at Monarch