LncRNA Information | ||||||
---|---|---|---|---|---|---|
ID | EL0668 | Name | LINC00850 | Aliases | KUCG1 | |
Species | Homo sapiens | Chromosome | X | Start site | 149825708 | |
End site | 149879799 | Chain | plus | Exon NO. | 3 | |
Assembly | Ensembl Release 89 | Class | lincRNA | NCBI accession | NR_109813 | |
Ensembl | ENSG00000280752 | Sequence |
Disease | |||||||||
---|---|---|---|---|---|---|---|---|---|
Disease | Method | Sample | Expression pattern | Dysfunction type | Description | PMID | Source | ||
Duchenne muscular dystrophy | N/A | N/A | N/A | mutation | Molecular characterization of an X(p21.2;q28) chromosomal inversion in a Duchenne muscular dystrophy patient with mental retardation reveals a novel long non-coding gene on Xq28 | 23223008 | LncRNADisease | ||
Duchenne muscular dystrophy | N/A | N/A | N/A | expression | KUCG1 is a 648-bp nuclear lncRNA expressed in a tissue specific manner. Since it is normally expressed in the brain, its deregulation could contribute to the neurological impairment of the patient as already reported for other pathologies. | 24685002 | LncRNADisease | ||