Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
100288077
Gene name Gene Name - the full gene name approved by the HGNC.
WTAP pseudogene 1
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
WTAPP1
Synonyms (NCBI Gene) Gene synonyms aliases
-
Chromosome Chromosome number
11
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
11q22.2
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
Multiple Sclerosis Multiple sclerosis N/A N/A GWAS
Associations from Text Mining Disease associations identified through Pubtator
Disease Name Relationship Type References
Carotid Artery Thrombosis Associate 40724896
Cholangitis Sclerosing Associate 21134112
Colitis Ulcerative Associate 21134112
Death Associate 21134112
Diabetic Angiopathies Associate 40724896
Eye Diseases Associate 23098370
Hemangioma Cavernous Central Nervous System Associate 26795600
Hypertension Associate 37181702
Kashin Beck Disease Associate 27245218
Laryngeal Neoplasms Associate 33015795