GNAS

GNAS complex locus
OMIM: 139320, Gene2Phenotype

17 panels

Panel Reviews Mode of inheritance Details
17 panels

Green GNAS in Brain Calcification


Level 2: Neurology and neurodevelopmental disorders
Version 1.96

Component of the following Super Panels:

  • Progressive Neurological Conditions
  • review MONOALLELIC, autosomal or pseudoautosomal, paternally imprinted (maternal allele expressed)
    Sources
    • Expert Review Green
    • Expert list
    Phenotypes
    • Pseudohypoparathyroidism Ib, MIM# 603233

    Amber GNAS in Craniosynostosis


    Level 2: Dysmorphic and congenital abnormality syndromes
    Version 1.68

    review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Amber
    • Expert list
    Phenotypes
    • Pseudohypoparathyroidism type 1a, MIM# 103580
    • Craniosynostosis

    Green GNAS in Mendeliome


    Version 1.1891

    review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Green
    • Victorian Clinical Genetics Services
    Phenotypes
    • Osseous heteroplasia, progressive (166350) AD
    • Pituitary adenoma 3, multiple types, somatic (617686)
    • Pseudohypoparathyroidism Ia (103580) AD
    • Pseudohypoparathyroidism Ib (603233) AD
    • Pseudohypoparathyroidism Ic (612462) AD
    • Pseudopseudohypoparathyroidism (612463)

    Green GNAS in Pseudohypoparathyroidism and Albright Hereditary Osteodystrophy


    Level 2: Endocrine disorders
    Version 0.13

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

    Green GNAS in Calcium and Phosphate disorders


    Level 2: Renal and urinary tract disorders; Endocrine disorders
    Version 1.24

    review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Green
    • Expert list
    Phenotypes
    • Pseudohypoparathyroidism Ia, MIM# 103580

    Green GNAS in Intellectual disability syndromic and non-syndromic


    Level 2: Neurology and neurodevelopmental disorders
    Version 0.6063

    review MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
    Sources
    • Expert Review Green
    • Genetic Health Queensland
    Phenotypes
    • Pseudohypoparathyroidism Ia (103580)
    • Pseudohypoparathyroidism Ib (603233)
    • Pseudohypoparathyroidism Ic (612462)
    • Pseudopseudohypoparathyroidism (612463)

    Green GNAS in Skeletal dysplasia

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

    review MONOALLELIC, autosomal or pseudoautosomal, paternally imprinted (maternal allele expressed)
    Sources
    • Expert Review Green
    • Expert Review Green
    • NHS GMS
    • Emory Genetics Laboratory
    • Victorian Clinical Genetics Services
    Phenotypes
    • Pseudohypoparathyroidism Ia 103580
    • ACTH-independent macronodular adrenal hyperplasia 219080 IC
    • Pseudohypoparathyroidism Ib 603233
    • Pseudopseudohypoparathyroidism 612463
    • McCune-Albright syndrome, somatic, mosaic 174800
    • Pseudohypoparathyroidism Ic 612462
    • Osseous heteroplasia, progressive 166350

    Green GNAS in Primary Ovarian Insufficiency_Premature Ovarian Failure

    Level 3: Gonadal and sex development disorders
    Level 2: Endocrine disorders
    Version 0.328

    review Not set
    Sources
    • Expert Review Green
    • Royal Melbourne Hospital

    Green GNAS in Additional findings_Paediatric


    Level 2: Screening
    Version 0.278

    review Unknown
    Sources
    • BabySeq Category A gene
    • Expert Review Green
    Phenotypes
    • Pseudopseudohypoparathyroidism
    • Pseudohypoparathyroidism

    Green GNAS in Congenital hypothyroidism

    Level 3: Thyroid disorders
    Level 2: Endocrine disorders
    Version 0.43

    review MONOALLELIC, autosomal or pseudoautosomal, paternally imprinted (maternal allele expressed)
    Sources
    • Expert Review Green
    • Genomics England PanelApp
    Phenotypes
    • Pseudohypoparathyroidism Ia, MIM#103580 (Hypothyroidism)

    Green GNAS in Mosaic skin disorders


    Level 2: Dermatological disorders
    Version 1.12

    Component of the following Super Panels:

  • Vascular Malformations SuperPanel
  • review MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
    Sources
    • Expert Review Green
    • Genomics England PanelApp
    • NHS GMS
    Phenotypes
    • McCune-Albright syndrome
    Tags
    • somatic

    Green GNAS in Imprinting disorders


    Version 1.3

    review MONOALLELIC, autosomal or pseudoautosomal, paternally imprinted (maternal allele expressed)
    Sources
    • Expert Review Green
    • Genomics England PanelApp
    Phenotypes
    • Affected tissue: kidney, bone, brain
    • pseudopseudohypoparathyroidism
    • Phenotype resulting from under expression: Pseudohypoparathyroidism Type 1a, MIM# 103580
    • Albright hereditary osteodystrophy

    Green GNAS 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, paternally imprinted (maternal allele expressed)
    Sources
    • Expert list
    • Expert Review Green
    Phenotypes
    • McCune-Albright syndrome, somatic, mosaic 174800
    • ACTH-independent macronodular adrenal hyperplasia 219080 IC
    • Osseous heteroplasia, progressive 166350
    • Pseudohypoparathyroidism Ic 612462
    • Pseudopseudohypoparathyroidism 612463
    • Pseudohypoparathyroidism Ia 103580
    • Pseudohypoparathyroidism Ib 603233

    Green GNAS in Fetal anomalies


    Version 1.255

    review MONOALLELIC, autosomal or pseudoautosomal, paternally imprinted (maternal allele expressed)
    Sources
    • Expert Review Green
    • Genomics England PanelApp
    Phenotypes
    • Pseudohypoparathyroidism Ia, MIM# 103580

    Green GNAS in Severe early-onset obesity


    Level 2: Endocrine disorders
    Version 1.10

    review MONOALLELIC, autosomal or pseudoautosomal, paternally imprinted (maternal allele expressed)
    Sources
    • Expert Review Green
    • Genomics England PanelApp
    Phenotypes
    • Pseudohypoparathyroidism Ia, MIM# 103580
    • Pseudohypoparathyroidism Ic, MIM# 612462
    • Pseudopseudohypoparathyroidism, MIM# 612463

    Green GNAS in BabyScreen+ newborn screening


    Level 2: Screening
    Version 1.113

    review MONOALLELIC, autosomal or pseudoautosomal, paternally imprinted (maternal allele expressed)
    Sources
    • Expert Review Green
    • BabySeq Category A gene
    Phenotypes
    • Pseudopseudohypoparathyroidism
    • Pseudohypoparathyroidism
    Tags
    • treatable
    • endocrine

    Green GNAS in Renal Tubulopathies and related disorders


    Level 2: Renal and urinary tract disorders
    Version 1.14

    Component of the following Super Panels:

  • Kidneyome_SuperPanel
  • review MONOALLELIC, autosomal or pseudoautosomal, paternally imprinted (maternal allele expressed)
    Sources
    • Expert Review Green
    • Expert list
    • Expert Review Green
    • Expert list
    Phenotypes
    • Pseudohypoparathyroidism Ic (612462) AD
    • Pituitary adenoma 3, multiple types, somatic (617686)
    • Pseudohypoparathyroidism Ia (103580) AD
    • Pseudohypoparathyroidism Ib (603233) AD
    • Osseous heteroplasia, progressive (166350) AD
    • Pseudopseudohypoparathyroidism (612463)