| LncRNA Information | ||||||
|---|---|---|---|---|---|---|
| ID | EL1230 | Name | SNHG4 | Aliases | NCRNA00059; U19H | |
| Species | Homo sapiens | Chromosome | 5 | Start site | 139273752 | |
| End site | 139283184 | Chain | plus | Exon NO. | 5 | |
| Assembly | GRCh38.p7 | Class | N/A | NCBI accession | NR_036536, NR_003141 | |
| Ensembl | N/A | Sequence | ||||
| Disease | |||||||||
|---|---|---|---|---|---|---|---|---|---|
| Disease | Method | Sample | Expression pattern | Dysfunction type | Description | PMID | Source | ||
| myelodysplastic syndrome | N/A | N/A | N/A | mutation | Association identified by GWAS. | 19240791 | LncRNADisease | ||