Monosomy Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description one chromosome missing from an otherwise diploid chromosome set (Mammalian Phenotype Ontology, MP_0004026)
External Link https://www.disgenet.org/browser/0/1/0/C0795878
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Genes

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

Symbol Name
ABL1 ABL proto-oncogene 1, non-receptor tyrosine kinase
ANPEP alanyl (membrane) aminopeptidase
BCL2 B-cell CLL/lymphoma 2
CD27 CD27 molecule
CD55 CD55 molecule, decay accelerating factor for complement (Cromer blood group)
CD69 CD69 molecule
CTNNA3 catenin (cadherin-associated protein), alpha 3
CTNND2 catenin (cadherin-associated protein), delta 2
ERBB2 erb-b2 receptor tyrosine kinase 2
ERG v-ets avian erythroblastosis virus E26 oncogene homolog
ESD esterase D
GPRC5D G protein-coupled receptor, class C, group 5, member D
IGH immunoglobulin heavy locus
KRAS Kirsten rat sarcoma viral oncogene homolog
MAF v-maf avian musculoaponeurotic fibrosarcoma oncogene homolog
MTTP microsomal triglyceride transfer protein
NF2 neurofibromin 2 (merlin)
NRAS neuroblastoma RAS viral (v-ras) oncogene homolog
PDGFB platelet-derived growth factor beta polypeptide
PDGFRB platelet-derived growth factor receptor, beta polypeptide
SAMD9L sterile alpha motif domain containing 9-like
SEMA5A sema domain, seven thrombospondin repeats (type 1 and type 1-like), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 5A
SHANK3 SH3 and multiple ankyrin repeat domains 3
SMARCB1 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily b, member 1
SOX11 SRY (sex determining region Y)-box 11
SRSF2 serine/arginine-rich splicing factor 2
ZAP70 zeta-chain (TCR) associated protein kinase 70kDa