slc35a3.1 Phenotypes

Phenotypes

XB-GENEPAGE-1011520

Gene Symbol: slc35a3.1 Gene Name: 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.
Computed annotations: slc35a3.1 assayed (4 sources)

Monarch Ortholog Phenotypes These phenotypes are associated with this gene with a has phenotype relation via Monarch.
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, Hypotonia, Intellectual disability, Intellectual disability, mild, Intellectual disability, moderate, Intellectual disability, severe, Knee dislocation, Microcephaly, Microretrognathia, Scoliosis, Seizure [+]
View all ortholog results at Monarch

Monarch Ortholog Phenotypes

These phenotypes are associated with this gene with a has phenotype relation via Monarch.

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, [+]