LINC01705 (long intergenic non-protein coding RNA 1705)

Gene
Gene Other IDs Associated diseases
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
107985307
Gene name Gene Name - the full gene name approved by the HGNC.
Long intergenic non-protein coding RNA 1705
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
LINC01705
Synonyms (NCBI Gene) Gene synonyms aliases
ERLR, LINC01655, LINC02257, TBUR1
Chromosome Chromosome number
1
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
1q41
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
Gene Other IDs Associated diseases
MIM HGNC e!Ensembl
HGNC 52493 N/A
<
Associated diseases Disease associations categorized as Causal (pathogenic variants), Unknown (uncertain genetic evidence), or Text Mining (literature-based associations)
Gene Other IDs Associated diseases
Show/Hide Unknown Diseases (2)
Unknown Includes: (1) ClinVar NON-pathogenic variants (Uncertain, Benign, Conflicting, VUS), (2) GenCC associations, (3) GWAS associations, (4) CBGDA evidence-based associations. NOTE: Diseases with pathogenic evidence are excluded to avoid conflicts.
Disease merge term Disease name Evidence References Source
Colorectal Cancer ICD10 C18, C19, C20: colorectal cancer, Early onset colorectal cancer, Colorectal cancer N/A N/A GWAS
Progressive Supranuclear Palsy Progressive supranuclear palsy N/A N/A GWAS