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Human Disease and Mouse Model Detail
Human Disease Peroxisome Biogenesis Disorder 1B; PBD1B
OMIM ID: 601539
Synonyms Adrenoleukodystrophy, Autosomal Neonatal; Infantile Phytanic Acid Storage Disease; Peroxisome Biogenesis Disorder; Peroxisome Biogenesis Disorder (nald/Ird); Peroxisome Biogenesis Disorder (neonatal Adrenoleukodystrophy/Infantile Refsum Disease); Refsum Disease, Infantile
Genes and
mouse models
Mutations in human and/or mouse homologs are associated with this disease

      *Gene is associated with the disease in this species
      Mouse Homologs Human Homologs Mouse Models Mouse : Human
Homology Class
     Pex1 PEX1*   1:1 Homology

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
07/23/2014
MGI 5.19
The Jackson Laboratory