prmt7 Phenotypes

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Phenotypes

Gene Literature (3)

Nucleotides (187)

Interactants (34)

XB-GENEPAGE-974625

Gene Symbol: prmt7 Gene Name: protein arginine methyltransferase 7

Monarch Ortholog Phenotypes These phenotypes are associated with this gene with a has phenotype relation via Monarch.
Human (31 sources): Anteverted nares, Astigmatism, Brachydactyly, Broad nasal tip, Deeply set eye, Delayed ability to walk, Delayed myelination, Delayed speech and language development, Depressed nasal bridge, Epicanthus, Frontal bossing, Generalized hypotonia, Global developmental delay, High palate, Intellectual disability, Long philtrum, Malar flattening, Microcephaly, Obesity, Pseudohypoparathyroidism, Retrognathia, Seizure, Short metacarpal, Short metatarsal, Short neck, Short palpebral fissure, Short stature, Strabismus, Thin vermilion border, Underdeveloped supraorbital ridges, Wide nasal bridge [+]
Mouse (30 sources): abnormal aortic valve morphology, abnormal cervical rib, abnormal coronary sinus connection, abnormal ductus venosus valve morphology, abnormal ductus venosus valve topology, abnormal hypoglossal nerve topology, abnormal inferior vena cava valve morphology, abnormal liver vasculature morphology, abnormal myoblast differentiation, abnormal response to injury, abnormal thymus topology, abnormal vitelline vein connection, abnormal vitelline vein topology, absent segment of posterior cerebral artery, blood in lymph vessels, decreased birth weight, decreased erythrocyte cell number, decreased lean body mass, decreased satellite cell number, decreased skeletal muscle weight, dual inferior vena cava, early cellular replicative senescence, embryo tumor, heterochrony, impaired skeletal muscle regeneration, increased epididymal fat pad weight, increased trigeminal neuroma incidence, retroesophageal right subclavian artery, subcutaneous edema, thoracoschisis [+]
View all ortholog results at Monarch