slc31a1 Phenotypes

Phenotypes

XB-GENEPAGE-994881

Gene Symbol: slc31a1 Gene Name: solute carrier family 31 (copper transporter), member 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: slc31a1 assayed (5 sources)

Monarch Ortholog Phenotypes These phenotypes are associated with this gene with a has phenotype relation via Monarch.
Mouse (23 sources): abnormal Reichert's membrane morphology, abnormal basement membrane morphology, abnormal embryonic neuroepithelium morphology, abnormal embryonic tissue morphology, abnormal liver copper level, abnormal mesenchyme morphology, abnormal mesoderm development, absent allantois, absent mesoderm, decreased Reichert's membrane thickness, decreased brain copper level, decreased circulating copper level, decreased embryo size, decreased liver iron level, decreased spleen weight, delayed neural tube closure, embryonic lethality during organogenesis, complete penetrance, failure of initiation of embryo turning, hemosiderosis, kinked vibrissae, postnatal lethality, incomplete penetrance, prenatal lethality, incomplete penetrance, thin endoderm [+]

Monarch Ortholog Phenotypes

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

Mouse (23 sources): abnormal Reichert's membrane morphology, abnormal basement membrane morphology, abnormal embryonic neuroepithelium morphology, abnormal embryonic tissue morphology, abnormal liver copper level, abnormal mesenchyme morphology, abnormal mesoderm development, absent allantois, absent mesoderm, decreased Reichert's membrane thickness, [+]