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Gene Gene information from NCBI Gene database.
Entrez ID 55384
Gene name Maternally expressed 3
Gene symbol MEG3
Synonyms (NCBI Gene)
FP504GTL2LINC00023NCRNA00023PRO0518PRO2160onco-lncRNA-83prebp1
Chromosome 14
Chromosome location 14q32.2
Summary This gene is a maternally expressed imprinted gene. Multiple alternatively spliced transcript variants have been transcribed from this gene and all of them are long non-coding RNAs (lncRNAs). This gene is expressed in many normal tissues, but its expressi
miRNA miRNA information provided by mirtarbase database.
18 Show/Hide all (18)
miRTarBase ID miRNA Experiments Reference
MIRT731765 hsa-miR-181a-5p Luciferase reporter assayqRT-PCRWestern blot 26253106
MIRT731765 hsa-miR-181a-5p Luciferase reporter assayqRT-PCRWestern blot 26253106
MIRT731765 hsa-miR-181a-5p Luciferase reporter assayqRT-PCRWestern blot 26253106
MIRT731765 hsa-miR-181a-5p Luciferase reporter assayqRT-PCRWestern blot 26253106
MIRT731765 hsa-miR-181a-5p Luciferase reporter assayqRT-PCRWestern blot 26253106
Transcription factors Transcription factors information provided by TRRUST V2 database.
1
Transcription factor Regulation Reference
CTCF Unknown 16331412
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
5
GO ID Ontology Definition Evidence Reference
GO:0006325 Process Chromatin organization IEA
GO:0016442 Component RISC complex IEA
GO:0030308 Process Negative regulation of cell growth IEA
GO:0035195 Process MiRNA-mediated post-transcriptional gene silencing IEA
GO:0141180 Function DsDNA-RNA triple helix-forming chromatin adaptor activity IDA 38456652
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
605636 14575 ENSG00000214548
Interactions View interactions
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
1
Evidence Score: ★☆☆☆☆  Gene-disease association found in Text Mining only ★★☆☆☆  Found in Text Mining and Unknown/Other Associations ★★★☆☆  Reported in Unknown/Other Associations across ≥2 Sources ★★★★☆  ClinVar: Pathogenic/Likely Pathogenic (<5 Variants) ★★★★★  ClinVar: Pathogenic/Likely Pathogenic (≥5 Variants)
Unknown / Other Associations ClinVar entries with uncertain/conflicting evidence, and associations from other databases (OMIM, Orphanet, GWAS, etc.) where the gene is not established as causal.
Phenotype Name Clinical Significance Source Reference Evidence Score
MEG3-related disorder Uncertain significance; Likely benign; Benign ClinVar —
★★★★★
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Associations from Text Mining Disease associations identified through text mining
Show/Hide Text Mining Associations (296)
Disease Name Disease (Merged) Source PMID Relationship Type Evidence Score
ACTH-Secreting Pituitary Adenoma Pituitary adenoma BEFREE 25126861
★★★★★
★☆☆☆☆
Found in Text Mining only
Adenocarcinoma of large intestine Colorectal Cancer BEFREE 30556866
★★★★★
★☆☆☆☆
Found in Text Mining only
Adenocarcinoma of lung (disorder) Lung adenocarcinoma BEFREE 25992654, 27338053, 31211438
★★★★★
★☆☆☆☆
Found in Text Mining only
Adenoma Adenoma BEFREE 30867789
★★★★★
★☆☆☆☆
Found in Text Mining only
Adrenal Gland Pheochromocytoma Adrenal Gland Pheochromocytoma BEFREE 31392726
★★★★★
★☆☆☆☆
Found in Text Mining only
Adult Hepatocellular Carcinoma Liver carcinoma BEFREE 21625215, 26321746
★★★★★
★☆☆☆☆
Found in Text Mining only
AICARDI-GOUTIERES SYNDROME Aicardi Goutieres Syndrome BEFREE 29749532
★★★★★
★☆☆☆☆
Found in Text Mining only
Alveolar rhabdomyosarcoma Alveolar Rhabdomyosarcoma BEFREE 24173021
★★★★★
★☆☆☆☆
Found in Text Mining only
Alzheimer Disease Alzheimer disease Pubtator 36895559 Associate
★★★★★
★☆☆☆☆
Found in Text Mining only
Anemia Anemia BEFREE 28814798
★★★★★
★☆☆☆☆
Found in Text Mining only