pofut1 Phenotypes

XB-GENEPAGE-979242

Gene Symbol: pofut1 Gene Name: protein O-fucosyltransferase 1

Monarch Ortholog Phenotypes These phenotypes are associated with this gene with a has phenotype relation via Monarch.
Human (4 sources): Follicular hyperkeratosis, Hyperkeratotic papule, Hypomelanotic macule, Reticular hyperpigmentation
Mouse (38 sources): abnormal atrioventricular cushion morphology, abnormal bronchiole epithelium morphology, abnormal cardiac epithelial to mesenchymal transition, abnormal dorsal-ventral polarity of the somites, abnormal heart development, abnormal mammary gland growth during pregnancy, abnormal somite development, abnormal somite shape, abnormal somite size, abnormal vasculogenesis, abnormal vertebral column morphology, abnormal vitelline vasculature morphology, absent club cells, absent intersomitic vessels, absent vertebral spinous process, absent vitelline blood vessels, decreased birth body size, decreased body length, decreased body size, decreased embryo size, distended pericardium, embryo phenotype, embryonic growth retardation, embryonic lethality during organogenesis, embryonic lethality during organogenesis, complete penetrance, epidermal cyst, failure of heart looping, fused somites, increased solitary pulmonary neuroendocrine cell number, kinked neural tube, kinked tail, myocardial trabeculae hypoplasia, postnatal lethality, incomplete penetrance, premature death, prenatal lethality, reproductive system phenotype, respiratory system phenotype, short tail [+]
View all ortholog results at Monarch