cfl1 Phenotypes

Phenotypes

XB-GENEPAGE-1016480

Gene Symbol: cfl1 Gene Name: cofilin 1 (non-muscle)

Monarch Ortholog Phenotypes These phenotypes are associated with this gene with a has phenotype relation via Monarch.
Mouse (30 sources): abnormal axon extension, abnormal cardiac outflow tract development, abnormal cerebral cortex morphology, abnormal eye development, abnormal neural crest cell delamination, abnormal neural crest cell migration, abnormal neural plate morphology, abnormal neurite morphology, abnormal neuron differentiation, abnormal neuronal precursor proliferation, abnormal podocyte foot process morphology, abnormal response to injury, abnormal somite border morphology, abnormal somite development, absent head mesenchyme, decreased embryo size, decreased embryonic neuroepithelial cell proliferation, decreased embryonic neuroepithelium thickness, disheveled coat, increased circulating creatinine level, open neural tube, pericardial edema, podocyte microvillus transformation, postnatal lethality, incomplete penetrance, premature death, premature neuronal precursor differentiation, prenatal lethality, complete penetrance, preweaning lethality, complete penetrance, renal/urinary system phenotype, wavy neural tube [+]

Monarch Ortholog Phenotypes

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

Mouse (30 sources): abnormal axon extension, abnormal cardiac outflow tract development, abnormal cerebral cortex morphology, abnormal eye development, abnormal neural crest cell delamination, abnormal neural crest cell migration, abnormal neural plate morphology, abnormal neurite morphology, abnormal neuron differentiation, abnormal neuronal precursor proliferation, [+]