PRKAR1A

protein kinase cAMP-dependent type I regulatory subunit alpha
OMIM: 188830, ClinGen, DECIPHER

18 panels

Panel Reviews Mode of inheritance Details
18 panels

Green PRKAR1A in Mendeliome


Version 2.0

1 review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • Acrodysostosis 1, with or without hormone resistance, MIM# 101800
  • Carney complex, type 1, MIM# 160980
  • Myxoma, intracardiac, MIM# 255960
  • Pigmented nodular adrenocortical disease, primary, 1, MIM# 610489

Green PRKAR1A in Cancer Predisposition_Paediatric


Level 2: Cancer
Version 1.0

0 reviews Unknown
Sources
  • Victorian Clinical Genetics Services
  • Expert Review Green

Green PRKAR1A in Pseudohypoparathyroidism and Albright Hereditary Osteodystrophy


Level 2: Endocrine disorders
Version 1.0

1 review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • Acrodysostosis 1, with or without hormone resistance, MIM# 101800

Green PRKAR1A in Additional findings_Adult


Level 2: Screening
Version 2.0

1 review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Green
  • Expert list
Phenotypes
  • Carney complex, type 1, MIM# 160980

Green PRKAR1A in Intellectual disability syndromic and non-syndromic


Level 2: Neurology and neurodevelopmental disorders
Version 2.0

1 review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Green
  • Genetic Health Queensland
Phenotypes
  • Acrodysostosis 1, with or without hormone resistance, MIM#101800

Green PRKAR1A in Skeletal dysplasia

Level 3: Skeletal dysplasias
Level 2: Skeletal disorders
Version 1.0

1 review BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Illumina TruGenome Clinical Sequencing Services
  • UKGTN
  • Radboud University Medical Center, Nijmegen
  • Expert Review Green
  • NHS GMS
  • Expert list
  • Emory Genetics Laboratory
  • Victorian Clinical Genetics Services
Phenotypes
  • Pigmented nodular adrenocortical disease, primary, 1 610489
  • Acrodysostosis 1, with or without hormone resistance 101800
  • Myxoma, intracardiac 255960

Green PRKAR1A in Additional findings_Paediatric


Level 2: Screening
Version 1.0

0 reviews MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • BabySeq Category A gene
  • Expert Review Green
Phenotypes
  • Carney complex

Green PRKAR1A in Incidentalome_PREGEN_DRAFT


Version 1.0

0 reviews Unknown
Sources
  • NSW Health Pathology
  • Expert Review Green

Green PRKAR1A in Congenital hypothyroidism

Level 3: Thyroid disorders
Level 2: Endocrine disorders
Version 1.0

1 review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Genomics England PanelApp
  • Expert Review Green
Phenotypes
  • Acrodysostosis, mild hormone resistance (TSH, PTH, GPCR-cAMP signalling hormones
  • Acrodysostosis 1, with or without hormone resistance, 101800

Green PRKAR1A in Hand and foot malformations


Level 2: Dysmorphic and congenital abnormality syndromes
Version 1.0

0 reviews BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Sources
  • Expert list
  • Expert Review Green
Phenotypes
  • Myxoma, intracardiac 255960
  • Acrodysostosis 1, with or without hormone resistance 101800
  • Pigmented nodular adrenocortical disease, primary, 1 610489

Green PRKAR1A in Fetal anomalies


Version 2.0

1 review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Green
  • Genomics England PanelApp
  • Genetic Health Queensland
Phenotypes
  • Acrodysostosis 1, with or without hormone resistance, MIM#101800

Green PRKAR1A in Genomic newborn screening: BabyScreen+


Level 2: Screening
Version 2.0

1 review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Green
  • BabySeq Category A gene
Phenotypes
  • Carney complex, type 1, MIM# 160980
Tags
  • treatable
  • cancer

Green PRKAR1A in Schwannoma


Level 2: Cancer Predisposition
Version 2.0

1 review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Green
  • Expert Review
  • Expert list
Phenotypes
  • Schwannoma, MONDO:0002546
  • Carney complex type 1, MONDO:0008057
  • Carney complex, type 1, MIM#160980

Green PRKAR1A in Thyroid Cancer


Level 2: Cancer Predisposition
Version 2.0

1 review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Green
  • Expert Review
  • Expert list
Phenotypes
  • Thyroid cancer, MONDO:0002108
  • Thyroid gland follicular carcinoma, MONDO:0005034
  • Carney complex type 1, MONDO:0008057
  • Carney complex, type 1, MIM#160980

Green PRKAR1A in Pituitary Tumour


Level 2: Cancer Predisposition
Version 2.0

1 review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Green
  • Expert Review
  • Expert list
Phenotypes
  • Pituitary tumor, MONDO:0017611
  • Pituitary gland adenoma, MONDO:0006373
  • Carney complex type 1, MONDO:0008057
  • Carney complex, type 1, MIM#160980

Red PRKAR1A in Paraganglioma_phaeochromocytoma


Level 2: Cancer Predisposition
Version 2.0

1 review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Red
  • Literature
  • Expert Review
  • Expert list
Phenotypes
  • Paraganglioma, MONDO:0000448
  • Pheochromocytoma, MONDO:0008233
  • Carney complex, type 1, MIM#160980

Green PRKAR1A in Hereditary Pigmentary Disorders


Level 2: Dermatological disorders
Version 2.0

2 reviews MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Green
  • Expert list
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • Carney complex, type 1 MONDO:0008057

Green PRKAR1A in Primary nodular adrenocortical disease

Level 3: Adrenal disorders
Level 2: Endocrine disorders; Cancer Predisposition
Version 1.0

1 review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Green
  • Expert List
Phenotypes
  • Pigmented nodular adrenocortical disease, primary, 1, MONDO:0012509
  • Carney complex type 1, MONDO:0008057