loxl3 Phenotypes

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Phenotypes

Gene Literature (1)

Nucleotides (79)

Interactants (16)

XB-GENEPAGE-5825438

Gene Symbol: loxl3 Gene Name: lysyl oxidase like 3

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: loxl3 assayed (3 sources)

Monarch Ortholog Phenotypes These phenotypes are associated with this gene with a has phenotype relation via Monarch.
Human (18 sources): Abnormality of epiphysis morphology, Amblyopia, Astigmatism, Cataract, Cleft palate, Epiphyseal dysplasia, Flat face, Genu valgum, Irregular vertebral endplates, Malar flattening, Micrognathia, Myopia, Platyspondyly, Retinal detachment, Sensorineural hearing impairment, Short stature, Vitreoretinopathy, obsolete Joint hyperflexibility [+]
Mouse (18 sources): abnormal chest morphology, abnormal craniofacial morphology, abnormal palate development, abnormal pulmonary alveolus morphology, abnormal spine curvature, abnormal vertebral body development, abnormal vertebral body morphology, abnormal vertebral column morphology, abnormal vomer bone morphology, cardiovascular system phenotype, failure of palatal shelf elevation, integument phenotype, neonatal lethality, incomplete penetrance, palatal shelves fail to meet at midline, postnatal lethality, complete penetrance, respiratory system phenotype, short mandible, vision/eye phenotype [+]
View all ortholog results at Monarch