cdh11 Phenotypes

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Phenotypes

Gene Literature (26)

Nucleotides (168)

Interactants (365)

XB-GENEPAGE-483598

Gene Symbol: cdh11 Gene Name: cadherin 11

Anatomical Phenotypes Phenotypes manually curated with terms from the Xenopus phenotype ontology covering anatomical, gene ontology, and neurobehavioral phenotypes.
absent branchial arch skeleton (1 source), decreased cell migration in branchial crest (1 source), decreased cell migration in cranial neural crest (1 source), decreased cell migration in hyoid crest (1 source), decreased cell migration in mandibular crest (1 source), decreased size of the chondrocranium (1 source), decreased size of the filopodium (1 source)

Expression Phenotypes Gene expression phenotype annotations where the gene of interest has been disrupted (manipulated) or is the gene assayed (assayed). Computed annotations are derived from differential expression analysis from Xenbase processed GEO data with the criteria of a TPM >= 1, FDR <= 0.05 and an absolute LogFC >= 2.
Computed annotations: cdh11 assayed (5 sources)

Experiments (Reagents) These are short form descriptions of experiments using reagents targeting the gene of interest.
Xla Wt + cdh11 MO (2 sources), Xla Wt + cdh11 MO + neural crest explant (1 source)

Monarch Ortholog Phenotypes These phenotypes are associated with this gene with a has phenotype relation via Monarch.
Human (88 sources): Abnormal dentin morphology, Abnormal sella turcica morphology, Abnormality of the cervical spine, Abnormality of the dentition, Abnormality of the shape of the midface, Abnormality of the vertebral column, Abnormality of the vertebral spinous processes, Absent external genitalia, Absent nipple, Advanced pneumatization of the mastoid process, Amelia involving the lower limbs, Anal stenosis, Anteriorly placed anus, Anteverted nares, Attached earlobe, Bifid scrotum, Bifid uvula, Bladder exstrophy, Blepharochalasis, Brachycephaly, Brachydactyly, Broad forehead, Broad nasal tip, Broad philtrum, Carious teeth, Cataract, Craniosynostosis, Cryptorchidism, Cutaneous syndactyly, Delayed eruption of teeth, Dental malocclusion, Depressed nasal bridge, Downslanted palpebral fissures, Downturned corners of mouth, Exodeviation, Eyelid coloboma, Facial asymmetry, Flat face, Glaucoma, Global developmental delay, High forehead, High palate, Highly arched eyebrow, Hypertelorism, Hypoplasia of the maxilla, Intellectual disability, Intellectual disability, moderate, Large earlobe, Long philtrum, Low hanging columella, Low-set ears, Malar flattening, Mandibular prognathia, Megalocornea, Microcephaly, Micropenis, Midface retrusion, Mixed hearing impairment, Multiple impacted teeth, Narrow forehead, Pectus excavatum, Penoscrotal hypospadias, Periorbital wrinkles, Phthisis bulbi, Pointed chin, Posteriorly rotated ears, Premature loss of teeth, Proptosis, Rootless teeth, Seizure, Short neck, Short philtrum, Strabismus, Submucous cleft hard palate, Synophrys, Telecanthus, Thick eyebrow, Thick lower lip vermilion, Thickened calvaria, Thin upper lip vermilion, Thin vermilion border, Thoracolumbar kyphoscoliosis, Umbilical hernia, Unilateral cleft palate, Upper limb peromelia, Ureteral stenosis, Wide intermamillary distance, Wide nasal bridge [+]
Mouse (1 source): embryo phenotype
View all ortholog results at Monarch