DCK, deoxycytidine kinase, 1633

N. diseases: 102; N. variants: 6
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs9993633
rs9993633
Entrez Id: 1633;92597
Gene Symbol: DCK;MOB1B
DCK;MOB1B
CUI: C1836232
Disease:
ACQUIRED IMMUNODEFICIENCY SYNDROME, PROGRESSION TO
A 0.700 GeneticVariation GWASCAT Association Between Single-Nucleotide Polymorphisms in HLA Alleles and Human Immunodeficiency Virus Type 1 Viral Load in Demographically Diverse, Antiretroviral Therapy-Naive Participants From the Strategic Timing of AntiRetroviral Treatment Trial. 31219150 2019
dbSNP: rs9993633
rs9993633
Entrez Id: 1633;92597
Gene Symbol: DCK;MOB1B
DCK;MOB1B
CUI: C1836233
Disease:
AIDS, PROGRESSION TO
A 0.700 GeneticVariation GWASCAT Association Between Single-Nucleotide Polymorphisms in HLA Alleles and Human Immunodeficiency Virus Type 1 Viral Load in Demographically Diverse, Antiretroviral Therapy-Naive Participants From the Strategic Timing of AntiRetroviral Treatment Trial. 31219150 2019
dbSNP: rs9993633
rs9993633
Entrez Id: 1633;92597
Gene Symbol: DCK;MOB1B
DCK;MOB1B
CUI: C1836231
Disease:
HIV-1, RESISTANCE TO
A 0.700 GeneticVariation GWASCAT Association Between Single-Nucleotide Polymorphisms in HLA Alleles and Human Immunodeficiency Virus Type 1 Viral Load in Demographically Diverse, Antiretroviral Therapy-Naive Participants From the Strategic Timing of AntiRetroviral Treatment Trial. 31219150 2019
dbSNP: rs9993633
rs9993633
Entrez Id: 1633;92597
Gene Symbol: DCK;MOB1B
DCK;MOB1B
CUI: C1836230
Disease:
HUMAN IMMUNODEFICIENCY VIRUS TYPE 1, SUSCEPTIBILITY TO
A 0.700 GeneticVariation GWASCAT Association Between Single-Nucleotide Polymorphisms in HLA Alleles and Human Immunodeficiency Virus Type 1 Viral Load in Demographically Diverse, Antiretroviral Therapy-Naive Participants From the Strategic Timing of AntiRetroviral Treatment Trial. 31219150 2019
dbSNP: rs9993633
rs9993633
Entrez Id: 1633;92597
Gene Symbol: DCK;MOB1B
DCK;MOB1B
CUI: C0376705
Disease:
Viral Load result
A 0.700 GeneticVariation GWASCAT Association Between Single-Nucleotide Polymorphisms in HLA Alleles and Human Immunodeficiency Virus Type 1 Viral Load in Demographically Diverse, Antiretroviral Therapy-Naive Participants From the Strategic Timing of AntiRetroviral Treatment Trial. 31219150 2019
dbSNP: rs9997790
rs9997790
Entrez Id: 1633;92597
Gene Symbol: DCK;MOB1B
DCK;MOB1B
CUI: C1304746
Disease:
RDW - Red blood cell distribution width result
0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs9997790
rs9997790
Entrez Id: 1633;92597
Gene Symbol: DCK;MOB1B
DCK;MOB1B
CUI: C0427460
Disease:
Red cell distribution width determination
0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs2306744
rs2306744
Entrez Id: 1633;92597
Gene Symbol: DCK;MOB1B
DCK;MOB1B
CUI: C1167791
Disease:
Skin toxicity
0.010 GeneticVariation BEFREE In addition, variant alleles of CDA rs532545 and rs602950 were related to skin toxicity (p = .031, p = .049) and mucositis to DCK rs2306744 minor allele (p = .046). 28573946 2017
dbSNP: rs2306744
rs2306744
Entrez Id: 1633;92597
Gene Symbol: DCK;MOB1B
DCK;MOB1B
CUI: C0521585
Disease:
Gastrointestinal mucositis
0.010 GeneticVariation BEFREE In addition, variant alleles of CDA rs532545 and rs602950 were related to skin toxicity (p = .031, p = .049) and mucositis to DCK rs2306744 minor allele (p = .046). 28573946 2017
dbSNP: rs4694362
rs4694362
Entrez Id: 1633
Gene Symbol: DCK
DCK
CUI: C0040034
Disease:
Thrombocytopenia
0.010 GeneticVariation BEFREE Other toxicities associated to variant alleles were hepatotoxicity to NT5C2 rs11598702 (p = .032), lung toxicity (p = .031) and thrombocytopenia to DCK rs4694362 (p = .046). 28573946 2017
dbSNP: rs4643786
rs4643786
Entrez Id: 1633
Gene Symbol: DCK
DCK
CUI: C0023467
Disease:
Leukemia, Myelocytic, Acute
0.010 GeneticVariation BEFREE DCK rs4643786 may serve as an independent predictor of drug response and AML outcome. 27548009 2016
dbSNP: rs67437265
rs67437265
Entrez Id: 1633
Gene Symbol: DCK
DCK
CUI: C1832661
Disease:
ANOPHTHALMIA AND PULMONARY HYPOPLASIA
0.010 GeneticVariation BEFREE Furthermore, 5 single-nucleotide polymorphisms (C1205T, A9846G, A70G, C356G, and C364T) of the dCK gene were detected in PDAC cells by PCR amplification and sequencing.The dCK protein expression was found to be negatively correlated with age (P = 0.006), but correlated positively with overall survival (OS) (P = 0.000) and disease-free survival (DFS) (P = 0.003). 26962792 2016
dbSNP: rs67437265
rs67437265
Entrez Id: 1633
Gene Symbol: DCK
DCK
CUI: C0023467
Disease:
Leukemia, Myelocytic, Acute
0.010 GeneticVariation BEFREE rs4643786 showed strong linkage disequilibrium with rs67437265. rs4643786 CT heterozygotes showed significantly higher complete remission rate (p = 0.028), superior overall survival (p = 0.006) and relapse-free survival (p = 0.020) than wild-type TT homozygotes. rs4643786 polymorphism was an independent predictor for AML prognosis. 27548009 2016
dbSNP: rs4643786
rs4643786
Entrez Id: 1633
Gene Symbol: DCK
DCK
CUI: C3839868
Disease:
Cytogenetically normal acute myeloid leukemia
0.010 GeneticVariation BEFREE We analyzed polymorphisms in genes encoding cytidine deaminase (CDA 79A>C rs2072671 and -451C>T rs532545), 5'-nucleotidase (cN-II 7A>G rs10883841), and deoxycytidine kinase (DCK 3'UTR 948T>C rs4643786) in 205 de novo NK-AML patients. 23873772 2013