Congenital Cytomegalovirus Infection Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
External Link https://www.disgenet.org/browser/0/1/0/C0158945
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Genes

24 genes associated with the disease Congenital Cytomegalovirus Infection in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
CXCR4 chemokine (C-X-C motif) receptor 4
DYRK1A dual-specificity tyrosine-(Y)-phosphorylation regulated kinase 1A
DYRK1B dual-specificity tyrosine-(Y)-phosphorylation regulated kinase 1B
ERVW-1 endogenous retrovirus group W, member 1
GJB2 gap junction protein, beta 2, 26kDa
GJB6 gap junction protein, beta 6, 30kDa
GPT glutamic-pyruvate transaminase (alanine aminotransferase)
IL1B interleukin 1, beta
ITGB2 integrin, beta 2 (complement component 3 receptor 3 and 4 subunit)
KLRC4-KLRK1 KLRC4-KLRK1 readthrough
KLRK1 killer cell lectin-like receptor subfamily K, member 1
KMT2A lysine (K)-specific methyltransferase 2A
LRP2 low density lipoprotein receptor-related protein 2
MCF2L MCF.2 cell line derived transforming sequence-like
NDUFS4 NADH dehydrogenase (ubiquinone) Fe-S protein 4, 18kDa (NADH-coenzyme Q reductase)
NHS Nance-Horan syndrome (congenital cataracts and dental anomalies)
RMND1 required for meiotic nuclear division 1 homolog (S. cerevisiae)
RNASET2 ribonuclease T2
SLC26A4 solute carrier family 26 (anion exchanger), member 4
TLR2 toll-like receptor 2
TLR4 toll-like receptor 4
TLR9 toll-like receptor 9
TNF tumor necrosis factor
TYRP1 tyrosinase-related protein 1