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LINC01798 (Long Intergenic Non-Protein Coding RNA 1798) is an RNA Gene, and is affiliated with the lncRNA class. Diseases associated with LINC01798 include Hereditary Hemorrhagic Telangiectasia.
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 |
---|---|---|---|---|---|---|---|---|---|---|
GH02J066572 | Promoter/Enhancer | 2.5 | EPDnew FANTOM5 Ensembl ENCODE CraniofacialAtlas dbSUPER | 600.7 | +4.6 | 4629 | 11.5 | RNF2 ARHGAP35 CEBPG GATAD2A CTCF PRDM10 ZNF512 IKZF1 ZNF692 FOXA1 | LINC01798 MEIS1 MEIS1-AS2 MEIS1-AS3 piR-60985-052 ETAA1 | |
GH02J066692 | Promoter/Enhancer | 1.8 | UCNEbase EPDnew Ensembl CraniofacialAtlas | 600.1 | +118.4 | 118439 | 3.6 | PRDM10 ZBTB44 CEBPB CBX2 PRDM6 POU5F1 | LINC01798 LINC01797 piR-39341-191 MEIS1 ETAA1 | |
GH02J066571 | Enhancer | 0.5 | UCNEbase ENCODE | 600.7 | -1.7 | -1700 | 0.8 | LINC01798 lnc-SPRED2-20 MEIS1 ETAA1 | ||
GH02J066565 | Enhancer | 1.5 | UCNEbase Ensembl ENCODE dbSUPER | 0.4 | -5.9 | -5886 | 4.7 | PRDM10 ZNF512 RFX1 JUND PKNOX1 POLR2A ZNF501 FOXJ2 EP300 SCRT2 | lnc-SPRED2-20 MEIS1 MEIS1-AS3 MEIS1-AS2 LINC01798 ETAA1 | |
GH02J066573 | Enhancer | 0.3 | UCNEbase | 0.7 | -2.2 | -2239 | 0.2 | LINC01798 lnc-SPRED2-20 MEIS1 ETAA1 |
RNAcentral Transcript ID | Subcategory | Length (nts) | # of Sources | Source Identifiers and Annotations |
---|---|---|---|---|
URS000075DC4A_9606 | lncRNA | 765 | 4 |
HGNC: 52588, RefSeq: NR_110156, LncBook: HSALNT0033050, LNCipedia: LINC01798:17, |
URS000027DA18_9606 | lncRNA | 555 | 4 |
Ensembl: ENST00000423168 (view in UCSC) , LncBook: HSALNT0033059, LNCipedia: LINC01798:19, NONCODE: NONHSAT071235.2, |
URS0000345EB0_9606 | lncRNA | 682 | 3 |
Ensembl: ENST00000433396 (view in UCSC) , LNCipedia: LINC01798:16, NONCODE: NONHSAT071233.2, |
URS00002C1661_9606 | lncRNA | 553 | 3 |
Ensembl: ENST00000428590 (view in UCSC) , LNCipedia: LINC01798:27, NONCODE: NONHSAT071238.2, |
URS000026D2E8_9606 | lncRNA | 528 | 3 |
Ensembl: ENST00000412944 (view in UCSC) , LNCipedia: LINC01798:28, NONCODE: NONHSAT071239.2, |
Variant ID | Type | Subtype | PubMed ID |
---|---|---|---|
esv3399130 | CNV | insertion | 20981092 |
esv3583854 | CNV | loss | 25503493 |
esv3583855 | CNV | loss | 25503493 |
esv3591123 | CNV | loss | 21293372 |
esv3591125 | CNV | loss | 21293372 |
esv3591126 | CNV | gain | 21293372 |
nsv1012523 | CNV | loss | 25217958 |
nsv476739 | CNV | novel sequence insertion | 20440878 |
nsv478925 | CNV | novel sequence insertion | 20440878 |
nsv522353 | CNV | loss | 19592680 |
nsv834248 | CNV | gain | 17160897 |
Disorder | Aliases | PubMed IDs |
---|---|---|
hereditary hemorrhagic telangiectasia |
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