PanelApp
  1. Genes and Genomic Entities
  2. BMP7

BMP7

bone morphogenetic protein 7
OMIM: 112267, Gene2Phenotype

4 panels

Panel Reviews Mode of inheritance Details
4 panels

Red BMP7 in Congenital anomalies of the kidney and urinary tract (CAKUT) Nonsyndromic


Level 2: Renal and urinary tract disorders
Version 0.127

Component of the following Super Panels:

  • Congenital abnormalities of the kidneys and urinary tract (CAKUT)_SuperPanel
  • Kidneyome_SuperPanel

    		•  2 reviews MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Red
    • Expert list
    Phenotypes
    • Congenital abnormalities of the kidneys and urinary tract

    Red BMP7 in Craniosynostosis


    Level 2: Dysmorphic and congenital abnormality syndromes
    Version 1.72

    		1 review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Red
    • Literature
    Phenotypes
    • Non-syndromic metopic craniosynostosis

    Red BMP7 in Differences of Sex Development


    Level 2: Dysmorphic and congenital abnormality syndromes
    Version 1.24

    		1 review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Red
    • Literature
    Phenotypes
    • Mayer-Rokitansky-Küster-Hauser syndrome (MRKHS)

    Red BMP7 in Mendeliome


    Version 1.3512

    		2 reviews MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Red
    • Literature
    Phenotypes
    • Congenital anomaly of kidney and urinary tract, MONDO:0019719, BMP7-related
    • Isolated craniosynostosis, MONDO:0015337, BMP7-related
    • Mayer-Rokitansky-Kuster-Hauser syndrome, MONDO:0017771, BMP7-related