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MALAT1 and diabetes mellitus are reported together in 4 articles.

Gene

MALAT1

HGNC
HGNC:29665
32articles
32mentions
2variants with confirmed gene link
Most co-reported phenotypes (articles)
Reported variants (articles · ClinVar status)
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

4 records shown · first 60
TypeEntitySource evidenceConfidenceExtractor
geneMALAT1“Associations of MALAT1 rs619586/rs3200401 and ANRIL rs10965215/rs10738605 polymorphisms with type 2 diabetes and diabetic nephropathy risk in an Egyptian population.”0.98hgnc_dict_v1
phenotypediabetes mellitus“Associations of MALAT1 rs619586/rs3200401 and ANRIL rs10965215/rs10738605 polymorphisms with type 2 diabetes and diabetic nephropathy risk in an Egyptian population.”0.93phenotype_alias_lexicon_v2
variantrs619586“Associations of MALAT1 rs619586/rs3200401 and ANRIL rs10965215/rs10738605 polymorphisms with type 2 diabetes and diabetic nephropathy risk in an Egyptian population.”0.90hgvs_regex_v1
variantrs3200401“Associations of MALAT1 rs619586/rs3200401 and ANRIL rs10965215/rs10738605 polymorphisms with type 2 diabetes and diabetic nephropathy risk in an Egyptian population.”0.90hgvs_regex_v1

Bridging autoimmunity and epigenetics: The influence of lncRNA MALAT1.

PMID 38199135 | DOI 10.1016/j.prp.2023.155041 · Pathology, research and practice · 2024 · 8 validated mentions
TypeEntitySource evidenceConfidenceExtractor
geneMALAT1“Bridging autoimmunity and epigenetics: The influence of lncRNA MALAT1.”0.98hgnc_dict_v1
phenotypediabetes mellitus“This review aims to elucidate the complex role of MALAT1 in autoimmune disorders, encompassing rheumatoid arthritis, multiple sclerosis, inflammatory bowel disease (Crohn's disease and ulcerative colitis), type 1 diabetes, systemic lupus erythematosus, and psoriasis.”0.93phenotype_alias_lexicon_v2
phenotypeinflammatory bowel disease“This review aims to elucidate the complex role of MALAT1 in autoimmune disorders, encompassing rheumatoid arthritis, multiple sclerosis, inflammatory bowel disease (Crohn's disease and ulcerative colitis), type 1 diabetes, systemic lupus erythematosus, and psoriasis.”0.98phenotype_alias_lexicon_v2
phenotypeulcerative colitis“This review aims to elucidate the complex role of MALAT1 in autoimmune disorders, encompassing rheumatoid arthritis, multiple sclerosis, inflammatory bowel disease (Crohn's disease and ulcerative colitis), type 1 diabetes, systemic lupus erythematosus, and psoriasis.”0.98phenotype_alias_lexicon_v2

Circulating long non-coding RNAs NKILA, NEAT1, MALAT1, and MIAT expression and their association in type 2 diabetes mellitus.

PMID 33436407 | PMCID PMC7805373 | DOI 10.1136/bmjdrc-2020-001821 · BMJ open diabetes research & care · 2021 · 6 validated mentions
TypeEntitySource evidenceConfidenceExtractor
geneMALAT1“Circulating long non-coding RNAs NKILA, NEAT1, MALAT1, and MIAT expression and their association in type 2 diabetes mellitus.”0.98hgnc_dict_v1
phenotypediabetes mellitus“Circulating long non-coding RNAs NKILA, NEAT1, MALAT1, and MIAT expression and their association in type 2 diabetes mellitus.”0.98phenotype_alias_lexicon_v2
geneNKILA“Circulating long non-coding RNAs NKILA, NEAT1, MALAT1, and MIAT expression and their association in type 2 diabetes mellitus.”0.98hgnc_dict_v1
geneNEAT1“Circulating long non-coding RNAs NKILA, NEAT1, MALAT1, and MIAT expression and their association in type 2 diabetes mellitus.”0.98hgnc_dict_v1

Long Non-Coding RNAs Gene Variants as Molecular Markers for Diabetic Retinopathy Risk and Response to Anti-VEGF Therapy.

PMID 34429633 | PMCID PMC8374537 | DOI 10.2147/PGPM.S322463 · Pharmacogenomics and personalized medicine · 2021 · 5 validated mentions
TypeEntitySource evidenceConfidenceExtractor
geneMALAT1“PURPOSE: For the first time, we aimed to evaluate the association of four lncRNAs TUG1 (rs7284767G/A), MIAT (rs1061540T/C), MALAT1 (rs3200401C/T), and SENCR (rs12420823C/T) variants with susceptibility to diabetic retinopathy (DR), disease severity, and early therapeutic response to intravitreous anti-vascular endothelial growth factor aflibercept therapy.”0.98hgnc_dict_v1
phenotypediabetes mellitus“PATIENTS AND METHODS: This case-control study enrolled 126 adult patients with type 2 diabetes.”0.93phenotype_alias_lexicon_v2
geneTUG1“PURPOSE: For the first time, we aimed to evaluate the association of four lncRNAs TUG1 (rs7284767G/A), MIAT (rs1061540T/C), MALAT1 (rs3200401C/T), and SENCR (rs12420823C/T) variants with susceptibility to diabetic retinopathy (DR), disease severity, and early therapeutic response to intravitreous anti-vascular endothelial growth factor aflibercept therapy.”0.98hgnc_dict_v1
geneMIAT“PURPOSE: For the first time, we aimed to evaluate the association of four lncRNAs TUG1 (rs7284767G/A), MIAT (rs1061540T/C), MALAT1 (rs3200401C/T), and SENCR (rs12420823C/T) variants with susceptibility to diabetic retinopathy (DR), disease severity, and early therapeutic response to intravitreous anti-vascular endothelial growth factor aflibercept therapy.”0.98hgnc_dict_v1