myl7 Phenotypes

Phenotypes

XB-GENEPAGE-964040

Gene Symbol: myl7 Gene Name: myosin light chain 7

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: myl7 assayed (2 sources)

Monarch Ortholog Phenotypes These phenotypes are associated with this gene with a has phenotype relation via Monarch.
Mouse (20 sources): abnormal atrioventricular cushion morphology, abnormal cardiac epithelial to mesenchymal transition, abnormal cardiac outflow tract development, abnormal heart looping, abnormal heart rate, abnormal heart tube morphology, abnormal intersomitic vessel morphology, abnormal myocardial fiber morphology, abnormal vasculogenesis, abnormal visceral yolk sac morphology, abnormal vitelline vascular remodeling, absent vitelline blood vessels, dilated heart left ventricle, embryonic growth arrest, embryonic growth retardation, embryonic lethality during organogenesis, complete penetrance, enlarged heart atrium, pericardial edema, trabecula carnea hypoplasia, ventricle myocardium hypoplasia [+]

Monarch Ortholog Phenotypes

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

Mouse (20 sources): abnormal atrioventricular cushion morphology, abnormal cardiac epithelial to mesenchymal transition, abnormal cardiac outflow tract development, abnormal heart looping, abnormal heart rate, abnormal heart tube morphology, abnormal intersomitic vessel morphology, abnormal myocardial fiber morphology, abnormal vasculogenesis, abnormal visceral yolk sac morphology, [+]