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Human Disease and Mouse Model Detail
Human Disease Pulmonary Fibrosis, Idiopathic; IPF
OMIM ID: 178500
Human Phenotype Ontology associations
Synonyms Fibrocystic Pulmonary Dysplasia; Fibrosing Alveolitis, Cryptogenic; Idiopathic Pulmonary Fibrosis, Familial
View all models View ALL (2) mouse models for this human disease.
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
     FOSL2 Fosl2* View 1 model HomoloGene and HGNC
TNF Tnf* View 1 model HomoloGene and HGNC
     MUC5B* Muc5b   HomoloGene and HGNC
SFTPA1*, SFTPA2* Sftpa1   HGNC
SFTPC* Sftpc   HomoloGene and HGNC
TERT* Tert   HomoloGene and HGNC
Transgenes and
other genome features
Transgenes and other genome features developed in mice to model this disease.

     Transgenes and Other Genome Features Mouse Models
  Tg(H2-K-Fosl2,EGFP)13Wag View 1 model
  Tg(SFTPC-Tnf)2Pva View 1 model
References Disease References using Mouse Models (2)

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