Disease Annotation

Gene Info

  • Species:Human (Homo sapiens)
  • GeneID:658
  • Symbol:BMPR1B
  • Description:bone morphogenetic protein receptor type 1B

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Disease_Term Source Rank Other Values
Brachydactyly, type A1, D, 616849 (3) OMIM high
  • Genome region :4q22.3
  • OMIM_ID :603248OMIM gene ID
  • OMIM_ID :616849OMIM phenotype ID
Acromesomelic dysplasia, Demirhan type, 609441 (3) OMIM high
  • Genome region :4q22.3
  • OMIM_ID :603248OMIM gene ID
  • OMIM_ID :609441OMIM phenotype ID
Brachydactyly, type A2, 112600 (3) OMIM high
  • Genome region :20p12.3
  • Genome region :20q11.22
  • Genome region :4q22.3
  • OMIM_ID :112261OMIM gene ID
  • OMIM_ID :112600OMIM phenotype ID
  • OMIM_ID :601146OMIM gene ID
  • OMIM_ID :603248OMIM gene ID
Amyotrophic lateral sclerosis (sporadic) GWAS high
Attention deficit hyperactivity disorder GWAS high