LncRNA Information
ID EL0878 Name MIR17HG Aliases C13orf25; FGLDS2; LINC00048; MIHG1; MIRH1; MIRHG1; NCRNA00048; miR-17-92
Species Homo sapiens Chromosome 13 Start site 91347820
End site 91354579 Chain plus Exon NO. 2
Assembly Ensembl Release 89 Class lincRNA NCBI accession NR_027350, NR_027349
Ensembl ENSG00000215417 Sequence


Disease
Disease Method Sample Expression pattern Dysfunction type Description PMID Source
cancer N/A N/A N/A locus Aurora kinase A induces miR-17-92 cluster through regulation of E2F1 transcription factor. 20300951 LncRNADisease
syndromic developmental defect N/A N/A N/A locus Here we report the identification of germline hemizygous deletions of MIR17HG, encoding the miR-17~92 polycistronic miRNA cluster, in individuals with microcephaly, short stature and digital abnormalities. 21892160 LncRNADisease
diffuse large B-cell lymphoma qPCR, Northern blot etc. cell lines (OCI-Ly4, OCI-Ly7, OCI-ly8 etc.) up-regulated locus C13orf25 (MIR17HG) is a target for 13q31-q32 amplification in malignant lymphoma. 15126345 LncRNADisease Lnc2Cancer
 


Interaction
Interaction target Level of interaction Type of interaction Description PMID Source
E2F1 DNA-TF regulation Aurora kinase A induces miR-17-92 cluster through regulation of E2F1 transcription factor. 20300951 LncRNADisease