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XB-GENEPAGE-987891
slc43a2 solute carrier family 43 (amino acid system L transporter), member 2
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: slc43a2 assayed (15 sources) |
| Monarch Ortholog Phenotypes
These phenotypes are associated with this gene with a has phenotype relation via Monarch.
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| Mouse (11 sources): abnormal amino acid level, abnormal amniotic fluid composition, abnormal intestinal absorption, abnormal placental transport, decreased fasting circulating glucose level, decreased fetal weight, fetal growth retardation, increased circulating carnitine level, increased fatty acids level, postnatal lethality, complete penetrance, [+] |