aldh1l2 Phenotypes

Phenotypes

XB-GENEPAGE-5820494

Gene Symbol: aldh1l2 Gene Name: aldehyde dehydrogenase 1 family member L2

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: aldh1l2 assayed (3 sources)

Monarch Ortholog Phenotypes These phenotypes are associated with this gene with a has phenotype relation via Monarch.
Mouse (18 sources): abnormal amino acid level, abnormal enzyme/coenzyme level, abnormal folic acid level, abnormal vitamin C level, behavior/neurological phenotype, cardiovascular system phenotype, decreased cystathionine level, decreased cysteine level, decreased fatty acid beta-oxidation, decreased glutathione level, endocrine/exocrine gland phenotype, growth/size/body region phenotype, immune system phenotype, liver/biliary system phenotype, nervous system phenotype, renal/urinary system phenotype, reproductive system phenotype, respiratory system phenotype [+]

Monarch Ortholog Phenotypes

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

Mouse (18 sources): abnormal amino acid level, abnormal enzyme/coenzyme level, abnormal folic acid level, abnormal vitamin C level, behavior/neurological phenotype, cardiovascular system phenotype, decreased cystathionine level, decreased cysteine level, decreased fatty acid beta-oxidation, decreased glutathione level, [+]