LTBP3

latent transforming growth factor beta binding protein 3
OMIM: 602090, Gene2Phenotype

9 panels

Panel Reviews Mode of inheritance Details
9 panels

Green LTBP3 in Skeletal Dysplasia_Fetal


Level 2: Skeletal disorders
Version 0.223

review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Green
  • Literature
Phenotypes
  • Geleophysic dysplasia 3 - MIM#617809

Green LTBP3 in Aortopathy_Connective Tissue Disorders


Level 2: Cardiovascular disorders
Version 1.85

review BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Other
Phenotypes
  • Thoracic aortic aneurysms and dissections

Green LTBP3 in Mendeliome


Version 1.1891

review BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • Dental anomalies and short stature, MIM# 601216
  • Geleophysic dysplasia 3, MIM# 617809
  • Thoracic aneurysm

Green LTBP3 in Skeletal dysplasia

Level 3: Skeletal dysplasias
Level 2: Skeletal disorders
Version 0.285

review MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Sources
  • Expert Review Green
  • Expert Review Green
  • Literature
  • NHS GMS
  • Victorian Clinical Genetics Services
Phenotypes
  • Dental anomalies and short stature 610216
  • Geleophysic dysplasia 3 617809
  • Geleophysic dysplasia 3 617809

Green LTBP3 in Mackenzie's Mission_Reproductive Carrier Screening


Level 2: Screening
Version 0.109

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Mackenzie's Mission
Phenotypes
  • Tooth agenesis, selective, 6, 613097 (3)

Green LTBP3 in Amelogenesis imperfecta


Level 2: Skeletal disorders
Version 1.10

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Genomics England PanelApp
Phenotypes
  • Dental anomalies and short stature, 601216
  • Amelogenesis Imperfecta
  • syndromic AI with brachyolmia

Green LTBP3 in Hand and foot malformations


Level 2: Dysmorphic and congenital abnormality syndromes
Version 0.74

Component of the following Super Panels:

  • Limb and Digital Malformations SuperPanel
  • review MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
    Sources
    • Expert list
    • Expert Review Green
    • Expert Review Green
    • Victorian Clinical Genetics Services
    Phenotypes
    • Geleophysic dysplasia 3 617809
    • Dental anomalies and short stature 610216

    Green LTBP3 in Fetal anomalies


    Version 1.255

    review BOTH monoallelic and biallelic, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • Genomics England PanelApp
    Phenotypes
    • Dental anomalies and short stature, MIM# 601216
    • Geleophysic dysplasia 3, MIM# 617809
    • Thoracic aneurysm

    Green LTBP3 in Prepair 1000+


    Level 2: Screening
    Version 1.9

    review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • Mackenzie's Mission
    Phenotypes
    • Tooth agenesis, selective, 6, 613097 (3)