MIR204 (microRNA 204)

Gene
Gene Gene ontology Other IDs Associated diseases
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
406987
Gene name Gene Name - the full gene name approved by the HGNC.
MicroRNA 204
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
MIR204
Synonyms (NCBI Gene) Gene synonyms aliases
MIRN204, RDICC, miRNA204, mir-204
Chromosome Chromosome number
9
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
9q21.12
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 Associated diseases
Show/Hide all(28)
GO ID Ontology Definition Evidence Reference
GO:0003730 Function MRNA 3'-UTR binding IDA 23204229
GO:0005615 Component Extracellular space HDA 26646931
GO:0008285 Process Negative regulation of cell population proliferation IDA 28280358
GO:0010669 Process Epithelial structure maintenance IDA 20056717
GO:0010719 Process Negative regulation of epithelial to mesenchymal transition IGI 23221074
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
Gene Gene ontology Other IDs Associated diseases
MIM HGNC e!Ensembl
610942 31582 ENSG00000207935
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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 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
Progressive Retinal Dystrophy-Iris Coloboma-Congenital Cataract Syndrome familial progressive retinal dystrophy-iris coloboma-congenital cataract syndrome N/A N/A GenCC
Show/Hide Text Mining Associations (108)
Associations from Text Mining Disease associations identified through Pubtator
Disease Name Relationship Type References
Acute Kidney Injury Associate 34240756
Acute Lung Injury Associate 34900201
Adenocarcinoma of Lung Associate 30840278
Alzheimer Disease Associate 36422510
Anemia Aplastic Associate 25187411
Anophthalmia with pulmonary hypoplasia Associate 26578390
Arthritis Rheumatoid Inhibit 29191214, 37498970
Arthritis Rheumatoid Associate 29577053
Atrial Fibrillation Associate 32478689, 37014905
beta Thalassemia Associate 34359863