Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
101928337
Gene name Gene Name - the full gene name approved by the HGNC.
Papillary thyroid carcinoma susceptibility candidate 2
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
PTCSC2
Synonyms (NCBI Gene) Gene synonyms aliases
-
Chromosome Chromosome number
9
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
9q22.33
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
HGNC N/A HGNC
<
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
Alopecia Areata Alopecia areata N/A N/A GWAS
Atrial Fibrillation Atrial fibrillation N/A N/A GWAS
Carcinoma Basal cell carcinoma N/A N/A GWAS
Hyperthyroidism Hyperthyroidism N/A N/A GWAS
Associations from Text Mining Disease associations identified through Pubtator
Disease Name Relationship Type References
Carcinoma Squamous Cell Associate 36333719
Cleft Lip Associate 39840623
Cleft Palate Associate 39840623
Colorectal Neoplasms Associate 36308369
Hashimoto Disease Associate 25303483
Nasopharyngeal Carcinoma Associate 37352861
Squamous Cell Carcinoma of Head and Neck Associate 35098409
Tertiary Lymphoid Structures Associate 26722557
Thyroid Cancer Papillary Inhibit 25303483
Thyroid Cancer Papillary Associate 25918370, 26722557, 27342578, 33551988, 37175943