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DLGAP1-AS2 (DLGAP1 Antisense RNA 2) is an RNA Gene, and is affiliated with the lncRNA class. Diseases associated with DLGAP1-AS2 include Astrocytoma and Chromosome 18P Deletion Syndrome.
RNAcentral Transcript ID | Subcategory | Length (nts) | # of Sources | Source Identifiers and Annotations |
---|---|---|---|---|
URS000075EE3F_9606 | lncRNA | 923 | 5 |
HGNC: 28146, RefSeq: NR_119377, LncBook: HSALNT0247196, LNCipedia: DLGAP1-AS2:2, NONCODE: NONHSAT177363.1, |
URS00002146CC_9606 | lncRNA | 2261 | 4 |
Ensembl: ENST00000572856 (view in UCSC) , LncBook: HSALNT0247197, LNCipedia: DLGAP1-AS2:4, NONCODE: NONHSAT057009.2, |
URS00001D649C_9606 | lncRNA | 1388 | 3 |
Ensembl: ENST00000573177 (view in UCSC) , LNCipedia: DLGAP1-AS2:1, NONCODE: NONHSAT057008.2, |
URS00008BB203_9606 | lncRNA | 2125 | 3 |
LncBook: HSALNT0247201, LNCipedia: DLGAP1-AS2:6, NONCODE: NONHSAT057011.2, |
URS00008BFCEF_9606 | lncRNA | 2239 | 2 |
LncBook: HSALNT0247198, LNCipedia: DLGAP1-AS2:3, |
Variant ID | Type | Subtype | PubMed ID |
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dgv184n21 | CNV | gain | 19592680 |
esv2490559 | CNV | insertion | 19546169 |
Disorder | Aliases | PubMed IDs |
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astrocytoma |
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chromosome 18p deletion syndrome |
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orofaciodigital syndrome viii |
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facioscapulohumeral muscular dystrophy 2 |
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