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XB-GENEPAGE-1011520
slc35a3.1 solute carrier family 35 (UDP-N-acetylglucosamine (UDP-GlcNAc) transporter), member A3, gene 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: slc35a3.1 assayed (4 sources) |
Monarch Ortholog Phenotypes
These phenotypes are associated with this gene with a has phenotype relation via Monarch.
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Human (20 sources): Arthrogryposis multiplex congenita, Autistic behavior, Camptodactyly of finger, Flexion contracture, Generalized hypotonia, Generalized non-motor (absence) seizure, Global developmental delay, Hammertoe, Hip dislocation, Hip dysplasia, [+] |
View all ortholog results at Monarch |