rhobtb2 Phenotypes

Phenotypes

XB-GENEPAGE-964294

Gene Symbol: rhobtb2 Gene Name: Rho related BTB domain containing 2

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.
Computed annotations: rhobtb2 assayed (4 sources)

Monarch Ortholog Phenotypes These phenotypes are associated with this gene with a has phenotype relation via Monarch.
Human (25 sources): Abnormal facial shape, Absent speech, Cerebellar hypoplasia, Cerebral cortical atrophy, Chorea, Delayed myelination, Depressed nasal bridge, Developmental regression, Dystonia, Epicanthus, Generalized hypotonia, Global developmental delay, Hemiparesis, Hypoplasia of the corpus callosum, Inability to walk, Intellectual disability, Limb hypertonia, Macrotia, Microcephaly, Micrognathia, Seizure, Smooth philtrum, Status epilepticus, Thin upper lip vermilion, Ventriculomegaly [+]
View all ortholog results at Monarch

Monarch Ortholog Phenotypes

These phenotypes are associated with this gene with a has phenotype relation via Monarch.

Human (25 sources): Abnormal facial shape, Absent speech, Cerebellar hypoplasia, Cerebral cortical atrophy, Chorea, Delayed myelination, Depressed nasal bridge, Developmental regression, Dystonia, Epicanthus, [+]