| ncRNA name | RP1-140A9.1 |
| ncRNA Category | lncRNA |
| ID | NA |
| Ensembl | NA |
| Synonyms | NA |
| Disease name | Volkmann cataract |
| Species | Homo sapiens |
| Tissues/Cell_line | blood |
| Methods | DNA sequencing, qRT-PCR, CLIP-seq |
| Expression pattern | associated |
| Functional description | The mutation in RP1-140A9.1 suggests the long non-coding RNA as the candidate cataract gene associated with the autosomal dominant inherited congenital cataract from CCV. The identified mutation, rs763295804, affects the donor splice site in the long non-coding RNA gene RP1-140A9.1 (ENSG00000231050). |
| PubMed ID | 30820140 |
| Year | 2019 |
| Title | A splice-site variant in the lncRNA gene RP1-140A9.1 cosegregates in the large Volkmann cataract family. |
| Drug-related ncRNA | NO |
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