irx5 iroquois homeobox 5
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: irx5 assayed (9 sources)|
|Monarch Ortholog Phenotypes
These phenotypes are associated with this gene with a has phenotype relation via Monarch.
Human (39 sources):
Abnormality of the outer ear,
Atrial septal defect,
Down-sloping shoulders, Dysphagia, High myopia, High palate, Hip dysplasia, Hypertelorism, Hypochromic anemia, Hypodontia, Hypoparathyroidism, Long philtrum, Long toe, Low posterior hairline, Low-set ears, Microcytic anemia, Micrognathia, Mitral regurgitation, Moderate global developmental delay, Osteopenia, Pectus excavatum, Preauricular skin tag, Sensorineural hearing impairment, Short 2nd finger, Smooth philtrum, Sparse lateral eyebrow, Syndactyly, Tapered finger, Webbed neck, Wide mouth, Wide nasal bridge[+]
|Mouse (2 sources): abnormal retina cone bipolar cell morphology, decreased body size|
View all ortholog results at Monarch