Carney Complex Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description An autosomal dominant disease characterized by myxomas, spotty pigmentation of the skin and endocrine overactivity. (Human Disease Ontology, DOID_0050471)
External Link https://www.disgenet.org/browser/0/1/0/C1837245
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Genes

77 genes associated with the disease Carney Complex in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
ACKR3 atypical chemokine receptor 3
ADO 2-aminoethanethiol (cysteamine) dioxygenase
ADRA1A adrenoceptor alpha 1A
ADRA2B adrenoceptor alpha 2B
AIP aryl hydrocarbon receptor interacting protein
APRT adenine phosphoribosyltransferase
ARR3 arrestin 3, retinal (X-arrestin)
ASMTL acetylserotonin O-methyltransferase-like
AZIN2 antizyme inhibitor 2
BRS3 bombesin-like receptor 3
CABLES1 Cdk5 and Abl enzyme substrate 1
CASR calcium-sensing receptor
CAT catalase
CAV1 caveolin 1, caveolae protein, 22kDa
CD19 CD19 molecule
CD247 CD247 molecule
CDKN1B cyclin-dependent kinase inhibitor 1B (p27, Kip1)
CETN1 centrin, EF-hand protein, 1
CTNNB1 catenin (cadherin-associated protein), beta 1, 88kDa
CXADR coxsackie virus and adenovirus receptor
CXCL2 chemokine (C-X-C motif) ligand 2
CXCR6 chemokine (C-X-C motif) receptor 6
CYP19A1 cytochrome P450, family 19, subfamily A, polypeptide 1
CYP2B6 cytochrome P450, family 2, subfamily B, polypeptide 6
CYP3A4 cytochrome P450, family 3, subfamily A, polypeptide 4
DICER1 dicer 1, ribonuclease type III
EDNRA endothelin receptor type A
GADL1 glutamate decarboxylase-like 1
GAL galanin/GMAP prepropeptide
GH1 growth hormone 1
GNA11 guanine nucleotide binding protein (G protein), alpha 11 (Gq class)
GNAS GNAS complex locus
GPR42 G protein-coupled receptor 42 (gene/pseudogene)
HCAR3 hydroxycarboxylic acid receptor 3
IGF1 insulin-like growth factor 1 (somatomedin C)
INHA inhibin, alpha
ITGA5 integrin, alpha 5 (fibronectin receptor, alpha polypeptide)
ITGAL integrin, alpha L (antigen CD11A (p180), lymphocyte function-associated antigen 1; alpha polypeptide)
ITGAV integrin, alpha V
ITGB2 integrin, beta 2 (complement component 3 receptor 3 and 4 subunit)
KCNJ2 potassium channel, inwardly rectifying subfamily J, member 2
KCNJ5 potassium channel, inwardly rectifying subfamily J, member 5
LPAR2 lysophosphatidic acid receptor 2
MAS1 MAS1 proto-oncogene, G protein-coupled receptor
MEN1 multiple endocrine neoplasia I
MFAP1 microfibrillar-associated protein 1
MPO myeloperoxidase
MSH2 mutS homolog 2
MTOR mechanistic target of rapamycin (serine/threonine kinase)
MYH8 myosin, heavy chain 8, skeletal muscle, perinatal
NR1I2 nuclear receptor subfamily 1, group I, member 2
NR1I3 nuclear receptor subfamily 1, group I, member 3
NR3C1 nuclear receptor subfamily 3, group C, member 1 (glucocorticoid receptor)
PDE11A phosphodiesterase 11A
POMC proopiomelanocortin
PRKACB protein kinase, cAMP-dependent, catalytic, beta
PRKAR1A protein kinase, cAMP-dependent, regulatory, type I, alpha
PRKAR1B protein kinase, cAMP-dependent, regulatory, type I, beta
PRL prolactin
PTBP2 polypyrimidine tract binding protein 2
PTEN phosphatase and tensin homolog
RCVRN recoverin
RET ret proto-oncogene
SDF4 stromal cell derived factor 4
SDHC succinate dehydrogenase complex, subunit C, integral membrane protein, 15kDa
SGSM3 small G protein signaling modulator 3
SLC8A1 solute carrier family 8 (sodium/calcium exchanger), member 1
SMARCA4 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 4
SMARCB1 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily b, member 1
SPG7 spastic paraplegia 7 (pure and complicated autosomal recessive)
SST somatostatin
SSTR4 somatostatin receptor 4
STK11 serine/threonine kinase 11
TRIM13 tripartite motif containing 13
UGT1A1 UDP glucuronosyltransferase 1 family, polypeptide A1
USP8 ubiquitin specific peptidase 8
WDR26 WD repeat domain 26