emg1 Phenotypes

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Phenotypes

Gene Literature (0)

Nucleotides (182)

Interactants (22)

XB-GENEPAGE-958955

Gene Symbol: emg1 Gene Name: EMG1 N1-specific pseudouridine methyltransferase

Monarch Ortholog Phenotypes These phenotypes are associated with this gene with a has phenotype relation via Monarch.
Human (21 sources): Abnormal cardiovascular system morphology, Abnormal joint morphology, Abnormal lung lobation, Camptodactyly of finger, Clinodactyly of the 5th finger, Cryptorchidism, Feeding difficulties in infancy, Joint stiffness, Microcephaly, Micrognathia, Orofacial cleft, Prominent nose, Rocker bottom foot, Seizure, Severe global developmental delay, Severe intrauterine growth retardation, Severe postnatal growth retardation, Short stature, Sloping forehead, Small for gestational age, Ventriculomegaly [+]
Mouse (26 sources): abnormal circulating aspartate transaminase level, abnormal embryo size, abnormal nucleolus morphology, abnormal placenta labyrinth morphology, abnormal preimplantation embryo development, abnormal retina inner nuclear layer morphology, abnormal retina outer nuclear layer morphology, abnormal telencephalon development, absent blastocoele, absent inner cell mass, decreased cell proliferation, decreased circulating aspartate transaminase level, decreased embryo size, decreased erythrocyte cell number, decreased startle reflex, decreased total retina thickness, embryonic growth arrest, embryonic growth retardation, embryonic lethality before implantation, complete penetrance, embryonic lethality during organogenesis, complete penetrance, embryonic lethality prior to organogenesis, incomplete rostral neuropore closure, increased apoptosis, open neural tube, preweaning lethality, complete penetrance, wavy neural tube [+]
View all ortholog results at Monarch