LncRNA Information | ||||||
---|---|---|---|---|---|---|
ID | EL0989 | Name | NPAP1 | Aliases | C15orf2 | |
Species | Homo sapiens | Chromosome | 15 | Start site | 24675868 | |
End site | 24683393 | Chain | plus | Exon NO. | 1 | |
Assembly | Ensembl Release 89 | Class | N/A | NCBI accession | N/A | |
Ensembl | ENSG00000185823 | Sequence | N/A |
Disease | |||||||||
---|---|---|---|---|---|---|---|---|---|
Disease | Method | Sample | Expression pattern | Dysfunction type | Description | PMID | Source | ||
Angelman syndrome | N/A | N/A | N/A | expression | C15orf2 and a novel noncoding transcript from the Prader-Willi/Angelman syndrome region show monoallelic expression in fetal brain. | 17337158 | LncRNADisease | ||
Prader-Willi syndrome | N/A | N/A | N/A | expression | C15orf2 and a novel noncoding transcript from the Prader-Willi/Angelman syndrome region show monoallelic expression in fetal brain. | 17337158 | LncRNADisease | ||