MIR122 (microRNA 122)

Gene
Gene Gene ontology Other IDs Pathways Associated diseases
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
406906
Gene name Gene Name - the full gene name approved by the HGNC.
MicroRNA 122
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
MIR122
Synonyms (NCBI Gene) Gene synonyms aliases
MIR122A, MIRN122, MIRN122A, hsa-mir-122, miRNA122, miRNA122A, mir-122
Chromosome Chromosome number
18
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
18q21.31
Summary Summary of gene provided in NCBI Entrez Gene.
microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase I
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
Gene Gene ontology Other IDs Pathways Associated diseases
Show/Hide all(5)
GO ID Ontology Definition Evidence Reference
GO:0005615 Component Extracellular space HDA 26646931
GO:0016442 Component RISC complex IEA
GO:0035195 Process MiRNA-mediated post-transcriptional gene silencing IEA
GO:0070062 Component Extracellular exosome IDA 28159509
GO:1903561 Component Extracellular vesicle HDA 28798470
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
Gene Gene ontology Other IDs Pathways Associated diseases
MIM HGNC e!Ensembl
609582 31501 ENSG00000284440
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
Gene Gene ontology Other IDs Pathways Associated diseases
  KEGG  
  MicroRNAs in cancer  
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Associated diseases Disease associations categorized as Causal (pathogenic variants), Unknown (uncertain genetic evidence), or Text Mining (literature-based associations)
Gene Gene ontology Other IDs Pathways Associated diseases
Show/Hide Unknown Diseases (1)
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
Diabetes Triglyceride levels in non-type 2 diabetes N/A N/A GWAS
Show/Hide Text Mining Associations (164)
Associations from Text Mining Disease associations identified through Pubtator
Disease Name Relationship Type References
3 Hydroxy 3 Methylglutaryl CoA Lyase Deficiency Associate 28377796
Abortion Spontaneous Associate 29393376
Achalasia Addisonianism Alacrimia syndrome Associate 23289041
Acute Coronary Syndrome Associate 27519051, 32846929
Acute On Chronic Liver Failure Associate 29540601
Adenocarcinoma of Lung Associate 24282590
Alstrom Syndrome Associate 36506055
Alzheimer Disease Inhibit 36221381
Angina Stable Associate 24260372
Arrhythmogenic Right Ventricular Dysplasia Associate 32102357