Related LncRNAs
ID	lncRNA Name	Disease	Method	Sample	Expression pattern	Dysfunction type	Description	PMID	Source
EL0289	CDKN2B-AS1	myocardial infarction	N/A	N/A	N/A	mutation	Association identified by GWAS.	17478679	LncRNADisease
EL0289	CDKN2B-AS1	myocardial infarction	N/A	N/A	N/A	mutation	association identified by GWAS (rs4977574, A>G).	19198609	LncRNADisease
EL0869	MIAT	myocardial infarction	N/A	N/A	N/A	mutation	In vitro functional analyses revealed that the minor variant of one SNP in exon 5 increased transcriptional level of MIAT. Moreover, unidentified nuclear protein(s) bound more intensely to risk allele than non-risk allele. These results indicate that the altered expression of MIAT by the SNP may play some role in the pathogenesis of MI.	17066261	LncRNADisease
EL0869	MIAT	myocardial infarction	N/A	N/A	N/A	mutation	SNPs associated with myocardial infarction localized to a haplotype block that encompassed the last 3 exons of MIAT.	20951849	LncRNADisease
EL0869	MIAT	myocardial infarction	N/A	N/A	N/A	mutation	MIAT lincRNA Variants Confer Susceptibility to Myocardial Infarction	23104877	LncRNADisease
EL0869	MIAT	myocardial infarction	N/A	N/A	N/A	regulation	A myocardial infarction-associated transcript (MIAT), also known as RNCR2 or Gomafu, is a long intergenic non-coding RNA that presents many genetic variants implicated in different processes. A large scale case-control association study regarding cardiovascular disease demonstrates that a MIAT variant (rs2301523) confers susceptibility to myocardial infarction.	24113581	LncRNADisease