CAV1

caveolin 1
OMIM: 601047, Gene2Phenotype

6 panels

Panel Reviews Mode of inheritance Details
6 panels

Green CAV1 in Interstitial Lung Disease


Level 2: Respiratory disorders
Version 1.0

review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Green
  • Expert list
Phenotypes
  • Pulmonary hypertension, primary, 3, MIM# 615343
  • Lipodystrophy, familial partial, type 7, MIM# 606721

Green CAV1 in Lipodystrophy_Lipoatrophy


Level 2: Dysmorphic and congenital abnormality syndromes
Version 1.17

review BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • Lipodystrophy, familial partial, type 7, autosomal dominant MIM# 606721
  • Lipodystrophy, congenital generalized, type 3, autosomal recessive, MIM# 612526

Green CAV1 in Mendeliome


Version 1.1891

review BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • Lipodystrophy, familial partial, type 7, autosomal dominant MIM# 606721
  • Lipodystrophy, congenital generalized, type 3, autosomal recessive, MIM# 612526

Red CAV1 in Monogenic Diabetes


Level 2: Endocrine disorders
Version 0.134

Component of the following Super Panels:

  • Metabolic Disorders Superpanel
  • review BOTH monoallelic and biallelic, autosomal or pseudoautosomal
    Sources
    • Expert Review Red
    Phenotypes
    • Lipodystrophy, congenital generalized, type 3, 612526
    • Partial lipodystrophy, congenital cataracts, and neurodegeneration syndrome

    Green CAV1 in Pulmonary Arterial Hypertension


    Level 2: Cardiovascular disorders
    Version 1.39

    review MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
    Sources
    • Expert Review Green
    • Expert list
    Phenotypes
    • Pulmonary hypertension, primary, 3 MIM#615343

    Green CAV1 in BabyScreen+ newborn screening


    Level 2: Screening
    Version 1.113

    review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • Expert list
    Phenotypes
    • Lipodystrophy, congenital generalized, type 3, MIM# 612526
    Tags
    • treatable
    • metabolic