Detail
LncRNA Name | H19 |
Synonyms | H19, ASM, ASM1, BWS, D11S813E, LINC00008, NCRNA00008, WT2 |
Region | GRCh38_11:1995176-2001470 Sequence |
Ensembl | ENSG00000130600 |
RefSeq | NR_002196 |
Circulating | ✘ |
Drug-resisitant | ✘ |
Prognostic | ✘ |
MiRNA | ✘ |
Variant | ✔ |
TF | ✘ |
Methylation | ✘ |
Cancer Name | bladder cancer |
ICD-0-3 | C67 |
Methods | qPCR etc. |
Sample | blood |
Expression Pattern | differential expression |
Function Description | A significantly decreased risk of bladder cancer was found for the rs2839698 TC genotype, but not for CC homozygotes. The rs2839698 TC genotype was especially associated with a reduced risk of developing non-muscle-invasive disease. Borderline significantly decreased risks of bladder cancer were found for the rs2107425 CT genotype, but not for TT homozygotes or for T allele carriers of rs217727. Haplotype analysis did not result in stronger associations with bladder cancer compared with the single-locus analyses. An SNP polymorphism in the nonî??protein-encoding H19 gene is associated with a decreased risk of developing nonî??muscleinvasive bladder cancer. This association was found for only heterozygotes, not for homozygotes. |
Pubmed ID | 18262338 |
Year | 2008 |
Title | Polymorphisms in the H19 gene and the risk of bladder cancer. |
External Links |
Links for H19 | GenBank HGNC lncrnadb Noncode |
Links for bladder cancer | Omim Cosmic |
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