CHURC1-FNTB (CHURC1-FNTB readthrough)
|
Gene
Gene information from NCBI Gene database.
|
|
| Entrez ID | 100529261 |
| Gene name | CHURC1-FNTB readthrough |
| Gene symbol | CHURC1-FNTB |
| Synonyms (NCBI Gene) |
FNTBFTase-beta
|
| Chromosome | 14 |
| Chromosome location | 14q23.3 |
| Summary | This locus represents naturally occurring read-through transcription between the neighboring CHURC1 (churchill domain containing 1) and FNTB (farnesyltransferase, CAAX box, beta) on chromosome 14. The read-through transcript produces a fusion protein that |
|
miRNA
miRNA information provided by mirtarbase database.
186
|
|||||||||||||||||||||||||
|
|||||||||||||||||||||||||
|
Other IDs
Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
|
|||||||
|
|||||||
|
Pathways
Pathway information has different metabolic/signaling pathways associated with genes.
|
|||||||||
|
|||||||||
|
Associated diseases
Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
4
|
|||||||||||||||||||||||||||||||
|
Evidence Score:
★☆☆☆☆ Gene-disease association found in Text Mining only
★★☆☆☆ Found in Text Mining and Unknown/Other Associations
★★★☆☆ Reported in Unknown/Other Associations across ≥2 Sources
★★★★☆ ClinVar: Pathogenic/Likely Pathogenic (<5 Variants)
★★★★★ ClinVar: Pathogenic/Likely Pathogenic (≥5 Variants)
|
|||||||||||||||||||||||||||||||
|
|||||||||||||||||||||||||||||||
|
|||||||||||||||||||||||||||||||