aldh7a1 Phenotypes

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Phenotypes

Gene Literature (2)

Nucleotides (215)

Interactants (100)

XB-GENEPAGE-492000

Gene Symbol: aldh7a1 Gene Name: aldehyde dehydrogenase 7 family member A1

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: aldh7a1 assayed (4 sources)

Monarch Ortholog Phenotypes These phenotypes are associated with this gene with a has phenotype relation via Monarch.
Human (21 sources): Abnormality of metabolism/homeostasis, Abnormality of movement, Bilateral tonic-clonic seizure, Cerebral cortical atrophy, Delayed speech and language development, EEG abnormality, Fetal distress, Generalized hypotonia, Generalized myoclonic seizure, Global developmental delay, Hepatomegaly, Hypotonia, Intellectual disability, Neonatal respiratory distress, Neurological speech impairment, Prenatal movement abnormality, Respiratory distress, Seizure, Status epilepticus, Strabismus, Ventriculomegaly [+]
Mouse (14 sources): abnormal amino acid level, abnormal vitamin level, behavior/neurological phenotype, decreased glycine level, decreased lysine level, increased circulating noradrenaline level, increased leucine level, increased ornithine level, increased phenylalanine level, increased proline level, increased serine level, no abnormal phenotype detected, oxidative stress, preweaning lethality, incomplete penetrance [+]
View all ortholog results at Monarch