LncRNA Information
ID	EL0653	Name	LINC00299	Aliases	C2orf46; NCRNA00299
Species	Homo sapiens	Chromosome	2	Start site	8007771
End site	8383621	Chain	minus	Exon NO.	9
Assembly	Ensembl Release 89	Class	lincRNA	NCBI accession	NR_034135
Ensembl	ENSG00000236790	Sequence

Disease
Disease	Method	Sample	Expression pattern	Dysfunction type	Description	PMID	Source
neurodevelopmental disabilities	DNA capture followed by next-generation sequencing	all tissues ,most abundantly in brain	N/A	N/A	these subjects with disruption of LINC00299 implicate this particular noncoding RNA in brain development and raise the possibility that, as a class, abnormalities of lincRNAs may play a significant role in human developmental disorders.	23217328
intellectual and developmental disability	N/A	N/A	N/A	mutation	Genetic variation in lncRNA genes causes disease and influences susceptibility	23791884	LncRNADisease