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 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