dph1 Phenotypes

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Phenotypes

Gene Literature (1)

Nucleotides (119)

Interactants (21)

XB-GENEPAGE-963021

Gene Symbol: dph1 Gene Name: diphthamide biosynthesis 1

Monarch Ortholog Phenotypes These phenotypes are associated with this gene with a has phenotype relation via Monarch.
Human (22 sources): Abnormality of the dentition, Abnormality of the kidney, Cerebellar vermis hypoplasia, Craniosynostosis, Dandy-Walker malformation, Depressed nasal bridge, Downslanted palpebral fissures, Epicanthus, Global developmental delay, Hypertelorism, Hypoplastic toenails, Intellectual disability, Low-set ears, Micrognathia, Prominent forehead, Scaphocephaly, Short stature, Sparse eyebrow, Sparse eyelashes, Sparse hair, Trigonocephaly, Ventricular septal defect [+]
Mouse (31 sources): abnormal craniofacial bone morphology, abnormal embryo turning, abnormal eye pigmentation, abnormal hepatoblast morphology, abnormal lung development, abnormal secondary palate development, abnormal skeleton development, abnormal somite development, absent palatine bone, craniofacial phenotype, decreased body size, decreased cranium length, decreased fetal weight, decreased fibroblast proliferation, decreased sensitivity to induced cell death, embryonic growth retardation, embryonic lethality during organogenesis, incomplete penetrance, embryonic lethality, complete penetrance, fetal growth retardation, increased nucleated erythrocyte cell number, increased tumor incidence, lethality at weaning, complete penetrance, mandible hypoplasia, neonatal lethality, complete penetrance, palatal shelves fail to meet at midline, postnatal lethality, incomplete penetrance, primary atelectasis, short Meckel's cartilage, short mandible, small cranium, thick lung-associated mesenchyme [+]
View all ortholog results at Monarch