Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
147081
Gene name Gene Name - the full gene name approved by the HGNC.
Long intergenic non-protein coding RNA 2210
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
LINC02210
Synonyms (NCBI Gene) Gene synonyms aliases
C17orf69, CRHR1-IT1
Chromosome Chromosome number
17
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
17q21.31
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
HGNC N/A HGNC
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Associated diseases Disease associations categorized as Causal (pathogenic variants), Unknown (uncertain genetic evidence), or Text Mining (literature-based associations)
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
Corticobasal Degeneration Corticobasal degeneration N/A N/A GWAS
Dementia Dementia N/A N/A GWAS
Diabetes Type 2 diabetes with neurological manifestations (PheCode 250.24) N/A N/A GWAS
Hypertrophic cardiomyopathy Hypertrophic cardiomyopathy N/A N/A GWAS