MIR96 (microRNA 96)

Gene Gene information from NCBI Gene database.
Gene Gene ontology Other IDs Pathways Associated diseases
Entrez ID 407053
Gene name MicroRNA 96
Gene symbol MIR96
Synonyms (NCBI Gene)
DFNA50MIRN96hsa-mir-96miR-96miRNA96
Chromosome 7
Chromosome location 7q32.2
Summary 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 (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
15
Gene Gene ontology Other IDs Pathways Associated diseases
Show/Hide all (15)
GO ID Ontology Definition Evidence Reference
GO:0003730 Function MRNA 3'-UTR binding IDA 25071021
GO:0010987 Process Negative regulation of high-density lipoprotein particle clearance IDA 23459944
GO:0016442 Component RISC complex IEA
GO:0035195 Process MiRNA-mediated post-transcriptional gene silencing IDA 23823476, 25071021, 30460077
GO:0035195 Process MiRNA-mediated post-transcriptional gene silencing IEA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
Gene Gene ontology Other IDs Pathways Associated diseases
MIM HGNC e!Ensembl
611606 31648 ENSG00000199158
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
Gene Gene ontology Other IDs Pathways Associated diseases
  KEGG 
  MicroRNAs in cancer  
Associated diseases Disease associations from ClinVar categorized as Causal (Pathogenic/Likely Pathogenic) or Unknown.
4
Gene Gene ontology Other IDs Pathways Associated diseases
Show/Hide Causal Diseases (1)
Causal Diseases associated with Pathogenic or Likely Pathogenic variants in ClinVar
Phenotype Name Clinical Significance dbSNP ID RCV Accession
Autosomal dominant nonsyndromic hearing loss 50 Pathogenic rs587776522, rs587776523 RCV000000913
RCV000000914
Show/Hide Unknown Diseases (2)
Unknown Diseases with uncertain, conflicting, or no pathogenic evidence in ClinVar
Phenotype Name Clinical Significance dbSNP ID RCV Accession
Hearing impairment Uncertain significance rs1425528986 RCV001375468
MIR96-related condition Uncertain significance rs375368092 RCV004758730
Show/Hide Text Mining Associations (86)
Associations from Text MiningDisease associations identified through Pubtator
Disease Name Relationship Type References
Adenoma Associate 30258124
Atrioventricular Septal Defect Associate 27396555
Breast Neoplasms Associate 19574223, 21203424, 25907662, 28793339, 32396572
Breast Neoplasms Stimulate 25394902, 27071841, 27857177
Carcinogenesis Associate 22045813, 24678958, 30258124
Carcinoma Hepatocellular Associate 21298008, 35475470, 35918602
Carcinoma Non Small Cell Lung Associate 22046296, 25286764
Carcinoma Non Small Cell Lung Stimulate 28445945
Carcinoma Ovarian Epithelial Associate 24816756
Carcinoma Pancreatic Ductal Associate 23776656, 31325400