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CDKN2A and diabetes mellitus are reported together in 5 articles.

Gene

CDKN2A

HGNC
HGNC:1787
48articles
48mentions
0variants with confirmed gene link
Most co-reported phenotypes (articles)
2,156articles
2,156mentions
12co-reported genes shown
Most co-reported genes (articles)

Counts are literature co-mentions in SaudiVarKB, not clinical or causal assertions. Gene details: HGNC; variant status: ClinVar via dbSNP.

Publications

5 records shown · first 60

Association Between CDKAL1, HHEX, CDKN2A/2B and IGF2BP2 Gene Polymorphisms and Susceptibility to Type 2 Diabetes in Uttarakhand, India.

PMID 33442279 | PMCID PMC7797276 | DOI 10.2147/DMSO.S284998 · Diabetes, metabolic syndrome and obesity : targets and therapy · 2021 · 9 validated mentions
TypeEntitySource evidenceConfidenceExtractor
geneCDKN2A“Association Between CDKAL1, HHEX, CDKN2A/2B and IGF2BP2 Gene Polymorphisms and Susceptibility to Type 2 Diabetes in Uttarakhand, India.”0.98hgnc_dict_v1
phenotypediabetes mellitus“Association Between CDKAL1, HHEX, CDKN2A/2B and IGF2BP2 Gene Polymorphisms and Susceptibility to Type 2 Diabetes in Uttarakhand, India.”0.93phenotype_alias_lexicon_v2
geneCDKAL1“Association Between CDKAL1, HHEX, CDKN2A/2B and IGF2BP2 Gene Polymorphisms and Susceptibility to Type 2 Diabetes in Uttarakhand, India.”0.98hgnc_dict_v1
geneHHEX“Association Between CDKAL1, HHEX, CDKN2A/2B and IGF2BP2 Gene Polymorphisms and Susceptibility to Type 2 Diabetes in Uttarakhand, India.”0.98hgnc_dict_v1

Genetics and genomics studies in type 2 diabetes: A brief review of the current scenario in the Arab region.

PMID 31336532 | DOI 10.1016/j.dsx.2019.03.017 · Diabetes & metabolic syndrome · 2019 · 18 validated mentions
TypeEntitySource evidenceConfidenceExtractor
geneCDKN2A“Studies from Egypt, Iraq, Jordan, Oman, Qatar, Saudi Arabia, Tunisia, and United Arab Emirates had been explored studying the associations of GIPR, ADIPOQ, FTO, (GRCh38.p12), MLXIP, AKNAD1, KCNJ11 CDKAL1, CDKN2A/2B, TCF7L2, ACE, SNAP25, ELMO1, VDR, KCTD8, GABRA4 and PRKD1 genes with T2D development.”0.98hgnc_dict_v1
phenotypediabetes mellitus“Genetics and genomics studies in type 2 diabetes: A brief review of the current scenario in the Arab region.”0.93phenotype_alias_lexicon_v2
geneGIPR“Studies from Egypt, Iraq, Jordan, Oman, Qatar, Saudi Arabia, Tunisia, and United Arab Emirates had been explored studying the associations of GIPR, ADIPOQ, FTO, (GRCh38.p12), MLXIP, AKNAD1, KCNJ11 CDKAL1, CDKN2A/2B, TCF7L2, ACE, SNAP25, ELMO1, VDR, KCTD8, GABRA4 and PRKD1 genes with T2D development.”0.98hgnc_dict_v1
geneADIPOQ“Studies from Egypt, Iraq, Jordan, Oman, Qatar, Saudi Arabia, Tunisia, and United Arab Emirates had been explored studying the associations of GIPR, ADIPOQ, FTO, (GRCh38.p12), MLXIP, AKNAD1, KCNJ11 CDKAL1, CDKN2A/2B, TCF7L2, ACE, SNAP25, ELMO1, VDR, KCTD8, GABRA4 and PRKD1 genes with T2D development.”0.98hgnc_dict_v1
TypeEntitySource evidenceConfidenceExtractor
geneCDKN2A“A fourth cluster (TCF7L2, SLC30A8, HHEX/IDE, CDKAL1, CDKN2A/2B) was defined by loci influencing insulin processing and secretion without a detectable change in fasting glucose levels.”0.98hgnc_dict_v1
phenotypediabetes mellitus“Impact of type 2 diabetes susceptibility variants on quantitative glycemic traits reveals mechanistic heterogeneity.”0.93phenotype_alias_lexicon_v2
genePPARG“The first cluster (PPARG, KLF14, IRS1, GCKR) was characterized by primary effects on insulin sensitivity.”0.98hgnc_dict_v1
geneKLF14“The first cluster (PPARG, KLF14, IRS1, GCKR) was characterized by primary effects on insulin sensitivity.”0.98hgnc_dict_v1
TypeEntitySource evidenceConfidenceExtractor
geneCDKN2A“CONCLUSIONS: We have shown for the first time that variants at WFS1, JAZF1, SLC30A8, CDKN2A/B, TCF7L2, KCNQ1, HMG20A, HNF4A and DUSP9 are associated with T2D in the Saudi population.”0.98hgnc_dict_v1
phenotypediabetes mellitus“Assessing the contribution of 38 genetic loci to the risk of type 2 diabetes in the Saudi Arabian Population.”0.93phenotype_alias_lexicon_v2
geneHNF4A“The effect sizes of these loci were comparable to those previously identified in other populations with the exception of HNF4A, which showed a trend for larger effect size in our study population (OR = 1·27) compared to that reported in South Asian populations (OR = 1·09; I(2) = 65·9).”0.98hgnc_dict_v1
geneSLC30A8“Analysis of a subgroup of subjects with BMI≤30 resulted in two additional loci (SLC30A8; P = 0·03, HMG20A; P = 0·02) showing significant association with T2D.”0.98hgnc_dict_v1
TypeEntitySource evidenceConfidenceExtractor
geneCDKN2A“Meanwhile PPARG-2 Pro12Ala, CDKN2A/2B rs10811661, IGF2BP2 rs4402960, HHEX rs7923837, CDKAL1 rs7754840, EXT2 rs1113132 and SLC30A8 rs13266634 were found to have no significant association with T2D among Arabs.”0.98hgnc_dict_v1
phenotypediabetes mellitus“ACE I/D and MTHFR C677T polymorphisms are significantly associated with type 2 diabetes in Arab ethnicity: a meta-analysis.”0.93phenotype_alias_lexicon_v2
geneACE“ACE I/D and MTHFR C677T polymorphisms are significantly associated with type 2 diabetes in Arab ethnicity: a meta-analysis.”0.98hgnc_dict_v1
geneMTHFR“ACE I/D and MTHFR C677T polymorphisms are significantly associated with type 2 diabetes in Arab ethnicity: a meta-analysis.”0.98hgnc_dict_v1