Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
399716
Gene name Gene Name - the full gene name approved by the HGNC.
Long intergenic non-protein coding RNA 2656
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
LINC02656
Synonyms (NCBI Gene) Gene synonyms aliases
-
Chromosome Chromosome number
10
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
10p15.1
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
HGNC 54142 N/A
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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
Rheumatoid arthritis Rheumatoid arthritis N/A N/A GWAS
Associations from Text Mining Disease associations identified through Pubtator
Disease Name Relationship Type References
Alopecia Associate 31908401
Arthritis Juvenile Associate 28990043
Arthritis Rheumatoid Associate 18794857
Diabetes Mellitus Type 1 Associate 20736230, 31455420
Disease Associate 25052311
Headache Associate 31908401
Tinnitus Associate 31908401
Uveomeningoencephalitic Syndrome Associate 31908401
Waardenburg Syndrome Associate 31908401