MIRLET7BHG (MIRLET7B host gene)

Gene
Gene Gene ontology Other IDs Associated diseases
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
400931
Gene name Gene Name - the full gene name approved by the HGNC.
MIRLET7B host gene
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
MIRLET7BHG
Synonyms (NCBI Gene) Gene synonyms aliases
PRR34-AS1, linc-Ppara
Chromosome Chromosome number
22
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
22q13.31
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(2)
GO ID Ontology Definition Evidence Reference
GO:0016442 Component RISC complex IEA
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 Associated diseases
MIM HGNC e!Ensembl
618216 37189 ENSG00000197182
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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 (2)
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
Ovarian cancer Epithelial ovarian cancer N/A N/A GWAS
Schizophrenia Schizophrenia N/A N/A GWAS
Show/Hide Text Mining Associations (3)
Associations from Text Mining Disease associations identified through Pubtator
Disease Name Relationship Type References
Lung Neoplasms Associate 26199339
Neoplasms Associate 34997014
Nervous System Diseases Associate 35661455