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XB-GENEPAGE-484662
prrx1 paired related homeobox 1
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.
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Computed annotations: prrx1 assayed (2 sources) |
Monarch Ortholog Phenotypes
These phenotypes are associated with this gene with a has phenotype relation via Monarch.
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Human (28 sources): Abnormal cranial nerve morphology, Abnormality of the orbital region, Abnormality of the outer ear, Absent nares, Agenesis of corpus callosum, Aglossia, Aplasia/Hypoplasia involving the nose, Aplasia/Hypoplasia of the cerebellum, Aplasia/Hypoplasia of the eyebrow, Cleft palate, [+] |
Mouse (46 sources): abnormal Meckel's cartilage morphology, abnormal artery morphology, abnormal cranium morphology, abnormal fetal ductus arteriosus morphology, abnormal forelimb zeugopod morphology, abnormal hindlimb zeugopod morphology, abnormal incudostapedial joint morphology, abnormal incus morphology, abnormal long bone hypertrophic chondrocyte zone, abnormal lung vasculature morphology, [+] |
View all ortholog results at Monarch |