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LINC01518 (Long Intergenic Non-Protein Coding RNA 1518) is an RNA Gene, and is affiliated with the lncRNA class. Diseases associated with LINC01518 include Hirschsprung Disease 1.
GeneHancer (GH) Identifier | GH Type | GH Score |
GH Sources | Gene Association Score | Total Score | TSS distance (kb) | Number of Genes Away | Size (kb) | Transcription Factor Binding Sites |
Gene Targets |
---|---|---|---|---|---|---|---|---|---|---|
GH10J042691 | Promoter | 0.6 | EPDnew | 250.7 | +0.3 | 332 | 0.1 | CTCF ZBTB33 CHD2 | LINC01518 piR-56861 ZNF33B BMS1 | |
GH10J042643 | Enhancer | 1.3 | Ensembl ENCODE dbSUPER | 0.3 | +46.2 | 46237 | 3.9 | TBP ZNF217 IKZF1 IRF2 MBD2 ELF1 ARNT ZNF395 REST NFATC3 | piR-47269 LINC00839 ZNF33B ZNF239 ENSG00000285884 piR-37597 LOC105378268 LINC01518 BMS1 | |
GH10J042652 | Enhancer | 1 | ENCODE dbSUPER | 0.3 | +38.3 | 38331 | 3 | IKZF1 ARNT VEZF1 NBN ZEB2 TAL1 RXRA NCOR1 ZNF316 IRF9 | piR-36427 LINC00839 ZNF32-AS2 BMS1 ZNF33B ZNF485 piR-37597 ENSG00000285884 LINC01518 | |
GH10J042689 | Enhancer | 0.3 | Ensembl | 0.7 | +2.3 | 2278 | 0.8 | ZNF316 | piR-56861 ZNF33B LOC441666 LINC01518 piR-50559 BMS1 | |
GH10J042650 | Enhancer | 0.4 | Ensembl | 0.3 | +41.6 | 41578 | 1 | EHMT2 ZBTB40 GABPB1 ETV6 | piR-37597 piR-47269 ZNF33B ENSG00000285884 LINC01518 BMS1 |
RNAcentral Transcript ID | Subcategory | Length (nts) | # of Sources | Source Identifiers and Annotations |
---|---|---|---|---|
URS000075CDAB_9606 | lncRNA | 1861 | 3 |
RefSeq: NR_120659, LNCipedia: LINC01518:6, NONCODE: NONHSAT156917.1, |
URS000075BE5D_9606 | lncRNA | 1850 | 2 |
RefSeq: NR_120656, LNCipedia: LINC01518:3, |
URS000075E771_9606 | lncRNA | 1743 | 2 |
RefSeq: NR_120657, LNCipedia: LINC01518:4, |
URS000075E88B_9606 | lncRNA | 1735 | 2 |
RefSeq: NR_120658, LNCipedia: LINC01518:5, |
URS0000EEEC8E_9606 | lncRNA | 1701 | 1 |
Ensembl: ENST00000668437 (view in UCSC) , |
Variant ID | Type | Subtype | PubMed ID |
---|---|---|---|
esv2665190 | CNV | deletion | 23128226 |
esv2671987 | CNV | deletion | 23128226 |
esv2759746 | CNV | loss | 17122850 |
esv2764213 | CNV | gain+loss | 21179565 |
esv33252 | CNV | loss | 17666407 |
esv34929 | CNV | loss | 17911159 |
esv3623020 | CNV | loss | 21293372 |
esv3623021 | CNV | loss | 21293372 |
esv3623022 | CNV | loss | 21293372 |
esv3623023 | CNV | loss | 21293372 |
esv3623024 | CNV | gain | 21293372 |
esv3891795 | CNV | gain | 25118596 |
nsv1042764 | CNV | gain | 25217958 |
nsv1046582 | CNV | gain | 25217958 |
nsv469725 | CNV | gain | 16826518 |
nsv550672 | CNV | gain | 21841781 |
nsv947887 | CNV | duplication | 23825009 |
nsv951563 | CNV | deletion | 24416366 |
Disorder | Aliases | PubMed IDs |
---|---|---|
hirschsprung disease 1 |
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