MIR96 (microRNA 96)

Gene
Gene Gene ontology Other IDs Pathways Associated diseases
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
407053
Gene name Gene Name - the full gene name approved by the HGNC.
MicroRNA 96
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
MIR96
Synonyms (NCBI Gene) Gene synonyms aliases
DFNA50, MIRN96, hsa-mir-96, miR-96, miRNA96
Chromosome Chromosome number
7
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
7q32.2
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(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 ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
Gene Gene ontology Other IDs Pathways Associated diseases
MIM HGNC e!Ensembl
611606 31648 ENSG00000199158
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 Causal Diseases (1)
Causal Diseases caused by PATHOGENIC or LIKELY PATHOGENIC variants from ClinVar only
Disease merge term Disease name dbSNP ID References
Deafness Autosomal dominant nonsyndromic hearing loss 50 rs587776522, rs587776523 N/A
Show/Hide Text Mining Associations (86)
Associations from Text Mining Disease 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