Disease Annotation

Gene Info

  • Species:Human (Homo sapiens)
  • GeneID:10516
  • Symbol:FBLN5
  • Description:fibulin 5

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Disease_Term Source Rank Other Values
Cutis laxa, autosomal dominant 2, 614434 (3) OMIM high
  • Genome region :14q32.12
  • OMIM_ID :604580OMIM gene ID
  • OMIM_ID :614434OMIM phenotype ID
Neuropathy, hereditary, with or without age-related macular degeneration, 608895 (3) OMIM high
  • Genome region :14q32.12
  • OMIM_ID :604580OMIM gene ID
  • OMIM_ID :608895OMIM phenotype ID
Cutis laxa, autosomal recessive, type IA, 219100 (3) OMIM high
  • Genome region :14q32.12
  • OMIM_ID :219100OMIM phenotype ID
  • OMIM_ID :604580OMIM gene ID
Macular degeneration, age-related, 3, 608895 (3) OMIM high
  • Genome region :14q32.12
  • OMIM_ID :604580OMIM gene ID
  • OMIM_ID :608895OMIM phenotype ID
Height GWAS high