Gene: protein kinase, cAMP-dependent, regulatory, type I, alpha; PRKAR1A


Gene Symbol: PRKAR1A
OMIM: 188830
Chromosome location: 17q24.2

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Pigmented nodular adrenocortical disease, primary, 1 || c.709-7_709-2delTTTTTA

Phenotype:    Pigmented nodular adrenocortical disease, primary, 1
Dna Change:    c.709-7_709-2delTTTTTA
Protein Change:   
Mutation Type:    Deletion
Mutation Effect:    Splice site
Location:    intron 6
Transcript:    NM_002734.4

PopulationEthnic GroupRegionMutation FrquencyCoalescence TimeReference
FranceNANA12 patients/12 unrelated familiesNAGroussin L et al., 2006Groussin L, Horvath A, Jullian E, Boikos S, Rene-Corail F, Lefebvre H, Cephise-Velayoudom FL, Vantyghem MC, Chanson P, Conte-Devolx B, Lucas M, Gentil A, Malchoff CD, Tissier F, Carney JA, Bertagna X, Stratakis CA, Bertherat J, . A PRKAR1A mutation associated with primary pigmented nodular adrenocortical disease in 12 kindreds.. J. Clin. Endocrinol. Metab.. 2006; 91(5):1943-9

References

Groussin L, Horvath A, Jullian E, Boikos S, Rene-Corail F, Lefebvre H, Cephise-Velayoudom FL, Vantyghem MC, Chanson P, Conte-Devolx B, Lucas M, Gentil A, Malchoff CD, Tissier F, Carney JA, Bertagna X, Stratakis CA, Bertherat J, A PRKAR1A mutation associated with primary pigmented nodular adrenocortical disease in 12 kindreds.J. Clin. Endocrinol. Metab.. 2006; 91(5):1943-9