PLS3

plastin 3
OMIM: 300131, Gene2Phenotype

8 panels

Panel Reviews Mode of inheritance Details
8 panels

Green PLS3 in Skeletal Dysplasia_Fetal


Level 2: Skeletal disorders
Version 0.223

review Unknown
Sources
  • Literature
  • Expert list
  • Victorian Clinical Genetics Services
  • Expert Review Green
  • Melbourne Genomics Health Alliance Perinatal Autopsy Flagship

Green PLS3 in Congenital diaphragmatic hernia


Level 2: Dysmorphic and congenital abnormality syndromes
Version 1.14

review X-LINKED: hemizygous mutation in males, biallelic mutations in females
Sources
  • Expert Review Green
  • Literature
Phenotypes
  • Diaphragmatic hernia 5, X-linked, MIM# 306950

Green PLS3 in Mendeliome


Version 1.1891

review X-LINKED: hemizygous mutation in males, biallelic mutations in females
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • Bone mineral density QTL18, osteoporosis - MIM#300910
  • Diaphragmatic hernia 5, X-linked, MIM# 306950

Green PLS3 in Osteogenesis Imperfecta and Osteoporosis


Level 2: Skeletal disorders
Version 0.114

review Unknown
Sources
  • Victorian Clinical Genetics Services
  • Expert Review Green

Green PLS3 in Skeletal dysplasia

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

review X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males)
Sources
  • Expert Review Green
  • Expert Review Green
  • Expert Review
  • NHS GMS
  • Victorian Clinical Genetics Services
Phenotypes
  • Bone mineral density QTL18, osteoporosis 300910

Green PLS3 in Fetal anomalies


Version 1.255

review X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males)
Sources
  • Expert Review Green
  • Literature
  • Expert list
Phenotypes
  • Bone mineral density QTL18, osteoporosis - MIM#300910
  • Diaphragmatic hernia 5, X-linked, MIM# 306950

Green PLS3 in BabyScreen+ newborn screening


Level 2: Screening
Version 1.113

review X-LINKED: hemizygous mutation in males, biallelic mutations in females
Sources
  • Expert Review Green
  • Expert list
Phenotypes
  • Bone mineral density QTL18, osteoporosis - MIM#300910
Tags
  • treatable
  • skeletal

Green PLS3 in Transplant Co-Morbidity Superpanel


Level 2: Screening
Version 0.18

review X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males)
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • Bone mineral density QTL18, osteoporosis