Gene Gene information from NCBI Gene database.
Entrez ID 100048912
Gene name CDKN2B and CDKN2A antisense cis and trans regulatory RNA 1
Gene symbol CDKN2B-AS1
Synonyms (NCBI Gene)
ANRILCDKN2B-ASCDKN2BASNCRNA00089PCAT12p15AS
Chromosome 9
Chromosome location 9p21.3
Summary This gene is located within the CDKN2B-CDKN2A gene cluster at chromosome 9p21. The gene product is a functional RNA molecule that interacts with polycomb repressive complex-1 (PRC1) and -2 (PRC2), leading to epigenetic silencing of other genes in this clu
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
1
GO ID Ontology Definition Evidence Reference
GO:0031507 Process Heterochromatin formation IEA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
613149 34341 ENSG00000240498
Interactions View interactions
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
1
Evidence Score: ★☆☆☆☆  Gene-disease association found in Text Mining only ★★☆☆☆  Found in Text Mining and Unknown/Other Associations ★★★☆☆  Reported in Unknown/Other Associations across ≥2 Sources ★★★★☆  ClinVar: Pathogenic/Likely Pathogenic (<5 Variants) ★★★★★  ClinVar: Pathogenic/Likely Pathogenic (≥5 Variants)
Unknown / Other Associations ClinVar entries with uncertain/conflicting evidence, and associations from other databases (OMIM, Orphanet, GWAS, etc.) where the gene is not established as causal.
Phenotype Name Clinical Significance Source Evidence Score
Three Vessel Coronary Disease Benign; Uncertain significance; protective; risk factor ClinVar
★★☆☆☆
Found in Text Mining + Unknown/Other Associations