ift52 Phenotypes

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Phenotypes

Gene Literature (4)

Nucleotides (111)

Interactants (51)

XB-GENEPAGE-982456

Gene Symbol: ift52 Gene Name: intraflagellar transport 52

Monarch Ortholog Phenotypes These phenotypes are associated with this gene with a has phenotype relation via Monarch.
Human (54 sources): Abnormal dental enamel morphology, Abnormal diaphysis morphology, Abnormal fingernail morphology, Abnormality of the dentition, Abnormal metaphysis morphology, Abnormal toenail morphology, Anteverted nares, Brachydactyly, Carious teeth, Clinodactyly of the 5th finger, Cone-shaped epiphyses of the phalanges of the hand, Craniosynostosis, Depressed nasal bridge, Disproportionate short-limb short stature, Dolichocephaly, Epicanthus, Everted lower lip vermilion, Finger syndactyly, Flat acetabular roof, Frontal bossing, Full cheeks, High forehead, High hypermetropia, Hypermetropia, Hypodontia, Hypoplasia of the corpus callosum, Hypotelorism, Low-set ears, Microdontia, Midface retrusion, Motor delay, Myopia, Narrow chest, Nystagmus, obsolete Joint hyperflexibility, Osteoporosis, Pectus excavatum, Postaxial polydactyly, Prominent occiput, Protuberant abdomen, Respiratory distress, Rhizomelia, Sandal gap, Short distal phalanx of finger, Short metacarpal, Short metatarsal, Short phalanx of finger, Short stature, Short thorax, Sparse hair, Taurodontia, Telecanthus, Widely spaced teeth, Wide nasal bridge [+]
Mouse (9 sources): abnormal embryo size, abnormal embryo turning, abnormal forebrain development, abnormal heart looping, abnormal midbrain development, abnormal visceral yolk sac morphology, embryonic lethality during organogenesis, complete penetrance, increased exploration in new environment, preweaning lethality, complete penetrance
View all ortholog results at Monarch