Entry |
|
Name |
Mutation-inactivated PRKAR1A to ACTH-cortisol signaling pathway
|
Definition |
(PRKAR1A*+PRKACA) -> (NR5A1,NR4A1,SP1,PBX1,CREB) => (STAR,CYP11B1) -> Cortisol |
Expanded |
(5573v1+5566) -> (2516,3164,6667,5087,10488,1385,1386,1388,148327,468,64764,84699,90993,9586) => (6770,1584) -> C00735 |
Class |
|
Type |
Variant
|
Pathway |
|
Disease |
H00260 | Pigmented micronodular adrenocortical disease |
|
Gene |
5573 | PRKAR1A; protein kinase cAMP-dependent type I regulatory subunit alpha |
5566 | PRKACA; protein kinase cAMP-activated catalytic subunit alpha |
2516 | NR5A1; nuclear receptor subfamily 5 group A member 1 |
3164 | NR4A1; nuclear receptor subfamily 4 group A member 1 |
6667 | SP1; Sp1 transcription factor |
5087 | PBX1; PBX homeobox 1 |
10488 | CREB3; cAMP responsive element binding protein 3 |
1385 | CREB1; cAMP responsive element binding protein 1 |
1386 | ATF2; activating transcription factor 2 |
1388 | ATF6B; activating transcription factor 6 beta |
148327 | CREB3L4; cAMP responsive element binding protein 3 like 4 |
468 | ATF4; activating transcription factor 4 |
64764 | CREB3L2; cAMP responsive element binding protein 3 like 2 |
84699 | CREB3L3; cAMP responsive element binding protein 3 like 3 |
90993 | CREB3L1; cAMP responsive element binding protein 3 like 1 |
9586 | CREB5; cAMP responsive element binding protein 5 |
6770 | STAR; steroidogenic acute regulatory protein |
1584 | CYP11B1; cytochrome P450 family 11 subfamily B member 1 |
|
Variant |
5573v1 (PRKAR1A*) PRKAR1A mutation
|
Metabolite |
|
Reference |
|
Authors |
Bonnet-Serrano F, Bertherat J |
Title |
Genetics of tumors of the adrenal cortex. |
Journal |
|
Reference |
|
Authors |
Lodish M, Stratakis CA |
Title |
A genetic and molecular update on adrenocortical causes of Cushing syndrome. |
Journal |
|
Reference |
|
Authors |
Lacroix A, Feelders RA, Stratakis CA, Nieman LK |
Title |
Cushing's syndrome. |
Journal |
|
Reference |
|
Authors |
Duan K, Gomez Hernandez K, Mete O |
Title |
Clinicopathological correlates of adrenal Cushing's syndrome. |
Journal |
|
LinkDB |
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