LncRNA Information
ID EL0346 Name DLG2-AS1 Aliases DLG2-AS; DLG2AS; PSZA11q14; SZ-1
Species Homo sapiens Chromosome 11 Start site 84594424
End site 84604599 Chain plus Exon NO. N/A
Assembly GRCh38.p7 Class N/A NCBI accession N/A
Ensembl N/A Sequence N/A


Disease
Disease Method Sample Expression pattern Dysfunction type Description PMID Source
schizophrenia N/A N/A N/A locus These results suggest that PSZA11q14 may be considered a candidate gene for schizophrenia acting as an antisense regulator of DLG-2, which controls assembling functional N-methyl-D-aspartate (NMDA) receptors. 13130513 LncRNADisease
myotonic dystrophy type 1 N/A N/A N/A mutation The mutant DMPK transcript causes myotonic dystrophy type 1 (DM1), which is encoded by a protein-coding gene containing a CUG expansion repeat in its 3'-untranslated region. 19909263 LncRNADisease
heart failure N/A N/A N/A expression it is clear that Nkx2-5 is a genetic modifier of myotonic muscular dystrophy RNA toxicity and indicates important functionality of this 3'UTR, independent of its mRNA, in heart dysfunction. 23104877 LncRNADisease