eftud2 Phenotypes

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Phenotypes

Gene Literature (2)

Nucleotides (304)

Interactants (119)

XB-GENEPAGE-972642

Gene Symbol: eftud2 Gene Name: elongation factor Tu GTP binding domain containing 2

Monarch Ortholog Phenotypes These phenotypes are associated with this gene with a has phenotype relation via Monarch.
Human (45 sources): Abnormal antihelix morphology, Abnormality of the outer ear, Absent tragus, Accessory oral frenulum, Anteverted nares, Atresia of the external auditory canal, Atrial septal defect, Choanal atresia, Cleft palate, Conductive hearing impairment, Deep philtrum, Delayed speech and language development, Downslanted palpebral fissures, Epicanthus, Esophageal atresia, Feeding difficulties, Feeding difficulties in infancy, Global developmental delay, Hypoplasia of the maxilla, Intellectual disability, Large earlobe, Low-set ears, Malar flattening, Mandibulofacial dysostosis, Microcephaly, Micrognathia, Microtia, Midface retrusion, Morphological abnormality of the middle ear, Overfolded helix, Preauricular skin tag, Preaxial hand polydactyly, Progressive microcephaly, Proximal placement of thumb, Respiratory distress, Secondary microcephaly, Seizure, Short nose, Short stature, Slender finger, Telecanthus, Trigonocephaly, Underdeveloped tragus, Upslanted palpebral fissure, Ventricular septal defect [+]
Mouse (13 sources): abnormal circulating cholesterol level, abnormal circulating total protein level, abnormal locomotor behavior, decreased circulating bilirubin level, decreased exploration in new environment, decreased grip strength, decreased large unstained cell number, decreased startle reflex, embryonic growth retardation, embryonic lethality at implantation, complete penetrance, neonatal lethality, incomplete penetrance, preweaning lethality, complete penetrance, reproductive system phenotype [+]
View all ortholog results at Monarch