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Human Disease and Mouse Model Detail
Human Disease Hyperlysinemia, Type I
OMIM ID: 238700
Human Phenotype Ontology associations
Synonyms Alpha-Aminoadipic Semialdehyde Synthase Deficiency; Hyperlysinemia; L-Lysine:NAD-Oxido-Reductase Deficiency; Lysine Intolerance; Lysine:Alpha-Ketoglutarate Reductase Deficiency
Genes and
mouse models
Mutations in human and/or mouse homologs are associated with this disease

      *Disease is associated/modeled with this Gene or a homolog. More...
      Human Homologs Mouse Homologs Mouse Models Homology Source
     AASS* Aass   HomoloGene and HGNC

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
MGI 6.07
The Jackson Laboratory