cwf19l1 Phenotypes

XB-GENEPAGE-995268

Gene Symbol: cwf19l1 Gene Name: CWF19 like cell cycle control factor 1

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: cwf19l1 assayed (1 source)

Monarch Ortholog Phenotypes These phenotypes are associated with this gene with a has phenotype relation via Monarch.
Human (30 sources): Abnormality of the distal phalanx of the thumb, Agenesis of corpus callosum, Babinski sign, Cerebellar hypoplasia, Cerebellar vermis hypoplasia, Clumsiness, Delayed speech and language development, Dysarthria, Dysmetria, Dystonia, Frequent falls, Gait ataxia, Generalized hypotonia, Global developmental delay, Horizontal nystagmus, Hyperreflexia, Hypotonia, Infantile muscular hypotonia, Intellectual disability, Intellectual disability, moderate, Intention tremor, Mild microcephaly, Monotonic speech, Nonprogressive cerebellar ataxia, Oculomotor apraxia, Slurred speech, Synophrys, Tremor, Truncal ataxia, Unsteady gait [+]
View all ortholog results at Monarch

Monarch Ortholog Phenotypes

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

Human (30 sources): Abnormality of the distal phalanx of the thumb, Agenesis of corpus callosum, Babinski sign, Cerebellar hypoplasia, Cerebellar vermis hypoplasia, Clumsiness, Delayed speech and language development, Dysarthria, Dysmetria, Dystonia, [+]