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XB-GENEPAGE-853094
alx1 ALX 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: alx1 assayed (8 sources) |
Monarch Ortholog Phenotypes
These phenotypes are associated with this gene with a has phenotype relation via Monarch.
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Human (33 sources): Absent eyebrow, Agenesis of corpus callosum, Aplasia/Hypoplasia of the frontal sinuses, Bifid nose, Brachycephaly, Brachydactyly, Camptodactyly of finger, Cataract, Cleft palate, Conductive hearing impairment, [+] |
Mouse (24 sources): abnormal nasal capsule morphology, abnormal palatine bone morphology, abnormal pectoral girdle bone morphology, absent gastric milk in neonates, absent interparietal bone, absent neurocranium, absent presphenoid bone, craniofacial phenotype, decreased cranium length, eyelids open at birth, [+] |
View all ortholog results at Monarch |