Familial Atypical Mole Melanoma Syndrome Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
External Link https://www.disgenet.org/browser/0/1/0/C2314896
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Genes

26 genes associated with the disease Familial Atypical Mole Melanoma Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
ACD adrenocortical dysplasia homolog (mouse)
BAP1 BRCA1 associated protein-1 (ubiquitin carboxy-terminal hydrolase)
BRCA2 breast cancer 2, early onset
CDK2 cyclin-dependent kinase 2
CDK4 cyclin-dependent kinase 4
CDKN2A cyclin-dependent kinase inhibitor 2A
CDKN2B cyclin-dependent kinase inhibitor 2B (p15, inhibits CDK4)
CHRM1 cholinergic receptor, muscarinic 1
HPRT1 hypoxanthine phosphoribosyltransferase 1
HRAS Harvey rat sarcoma viral oncogene homolog
IFNA1 interferon, alpha 1
IFNA13 interferon, alpha 13
IFNA17 interferon, alpha 17
IFNA2 interferon, alpha 2
MC1R melanocortin 1 receptor (alpha melanocyte stimulating hormone receptor)
MGMT O-6-methylguanine-DNA methyltransferase
MITF microphthalmia-associated transcription factor
MYCL v-myc avian myelocytomatosis viral oncogene lung carcinoma derived homolog
NPPA natriuretic peptide A
POT1 protection of telomeres 1
PTH parathyroid hormone
TERF2IP telomeric repeat binding factor 2, interacting protein
TERT telomerase reverse transcriptase
TP53 tumor protein p53
TYR tyrosinase
XPA xeroderma pigmentosum, complementation group A