Related LncRNAs
ID	lncRNA Name	Disease	Method	Sample	Expression pattern	Dysfunction type	Description	PMID	Source
EL0289	CDKN2B-AS1	Stroke	N/A	N/A	N/A	expression	Significantly reduced expression of all INK4/ARF transcripts (p15(INK4b), p16(INK4a), ARF and ANRIL) was found in PBTL of individuals harboring a common SNP (rs10757278) associated with increased risk of coronary artery disease, stroke and aortic aneurysm.	19343170	LncRNADisease
EL0289	CDKN2B-AS1	Stroke	N/A	N/A	N/A	mutation	Risk SNPs (rs3217992, A>G;rs1063192, C>T) for coronary disease, stroke, diabetes, melanoma, and glioma were all associated with allelic expression of ANRIL.	20386740	LncRNADisease Lnc2Cancer
EL0289	CDKN2B-AS1	Stroke	N/A	N/A	N/A	mutation	Variants (rs3217992, A>G;rs1063192, C>T) on chromosome 9p21.3 correlated with ANRIL expression contribute to stroke risk and recurrence in a large prospective stroke population.	22034006	LncRNADisease
EL0289	CDKN2B-AS1	Stroke	N/A	N/A	N/A	mutation	Moreover, genome-wide association studies have demonstrated that the 9p21 genomic locus is a hotspot for the risk of stroke, glioma, plexiform neurofibroma and other disorders	22814587	LncRNADisease
EL0289	CDKN2B-AS1	Stroke	N/A	N/A	N/A	expression	Genetic variants that affect the expression of the ANRIL transcript have been correlated with stroke risk and recurrence in a large prospective study	22817756	LncRNADisease
EL0289	CDKN2B-AS1	Stroke	N/A	N/A	N/A	mutation	Genetic variation in lncRNA genes causes disease and influences susceptibility	23791884	LncRNADisease
EL0289	CDKN2B-AS1	Stroke	N/A	N/A	N/A	expression	Levels of CDKN2B-AS1/ANRIL in human carotid atherosclerotic plaques and peripheral blood T lymphocytes are linked to rates of ischemic and hemorrhagic stroke.	24145019	LncRNADisease