Entry Detail


General Information

Database ID: LDA0016062
Species: Homo sapiens
Confidence Score: 0.731059
Contents: >> ncRNA Information
>> ncRNA Association Statistics
>> Disease Information
>> Disease Association Statistics
>> Evidence Support
>> Reference
Causality: Unknown
Clinical Significance: Unknown

 


ncRNA Information

Reference Genome Note: GRCh38 for human lncRNAs; GRCm39 for mouse lncRNAs; mRatBN7.2 for rat lncRNAs; hg19 for human circRNAs; mm9 for mouse circRNAs.

ncRNA Symbol:MIAT
Full Name:myocardial infarction associated transcript
Category:LncRNA
Species:Homo sapiens
Synonyms:C22orf35|GOMAFU|LINC00066|NCRNA00066|RNCR2|lncRNA-MIAT
Chromosome:22
Strand:+
Coordinate:
Start Site(bp):26657482End Site(bp):26676478
External Links:
Ensembl ID:ENSG00000225783
Ensembl Transcript ID:N/A
Entrez Gene:440823.0
NONCODE ID:N/A
RefSeq Accession:N/A

 

ncRNA Association Statistics

Total Associated Disease Number:66   
More Information
Causal Disease Number:52
Network:
Top Causal Diseases:
Breast Neoplasms  (Score: 0.999998)
Breast Neoplasms  (Score: 0.999998)
Stomach Neoplasms  (Score: 0.999893)
Carcinoma, Hepatocellular  (Score: 0.999893)
Carcinoma, Hepatocellular  (Score: 0.999893)
Stomach Neoplasms  (Score: 0.999893)
Thyroid Cancer, Papillary  (Score: 0.985791)
Diabetic Nephropathies  (Score: 0.985791)
acute myocardial infarction  (Score: 0.985791)
Uterine Cervical Neoplasms  (Score: 0.985791)
More Information

 

 

Disease Information

 Disease OntologyMeSH
Disease ID:D017086
Disease Name:beta-Thalassemia
Category:MeSH
Type:Hemic and Lymphatic Diseases
Define:A disorder characterized by reduced synthesis of the beta chains of hemoglobin. There is retardation of hemoglobin A synthesis in the heterozygous form (thalassemia minor), which is asymptomatic, while in the homozygous form (thalassemia major, Cooley's anemia, Mediterranean anemia, erythroblastic anemia), which can result in severe complications and even death, hemoglobin A synthesis is absent.
Alias:beta-Thalassemia//Microcytemia, beta Type//Microcytemias, beta Type//Type Microcytemia, beta//Type Microcytemias, beta//beta Type Microcytemia//beta Type Microcytemias//beta Thalassemia//Thalassemia, beta//Thalassemias, beta//beta Thalassemias//Thalassemia, beta Type//Thalassemias, beta Type//Type Thalassemia, beta//Type Thalassemias, beta//beta Type Thalassemia//beta Type Thalassemias//Thalassemia Intermedia//Intermedia, Thalassemia//Intermedias, Thalassemia//Thalassemia Intermedias//Thalassemia Minor//Thalassemia Minor (beta-Thalassemia Minor)//Minor, Thalassemia (beta-Thalassemia Minor)//Minors, Thalassemia (beta-Thalassemia Minor)//Thalassemia Minor (beta Thalassemia Minor)//Thalassemia Minors (beta-Thalassemia Minor)//Hemoglobin F Disease//Disease, Hemoglobin F//Thalassemia Major//Anemia, Erythroblastic//Anemias, Erythroblastic//Erythroblastic Anemia//Thalassemia Major (beta-Thalassemia Major)//Major, Thalassemia (beta-Thalassemia Major)//Majors, Thalassemia (beta-Thalassemia Major)//Thalassemia Major (beta Thalassemia Major)//Thalassemia Majors (beta-Thalassemia Major)//Mediterranean Anemia//Anemias, Mediterranean//Mediterranean Anemias//Anemia, Cooley's//Anemia, Cooley//Anemia, Cooleys//Cooley's Anemia//Anemia, Mediterranean

 

Disease Association Statistics

Total Associated ncRNA Number:6   
More Information
Causal ncRNA Number:0
Network:
Top Causal ncRNAs:
More Information

 

Evidence Support

Strong Evidence:qRT-PCR
Weak Evidence:

 

Reference

[1] PubMed ID:30665334
Disease Name:beta-Thalassemia
Sample:blood
Dysfunction Pattern:Expression[highly expressed]
Validated Method:qRT-PCR
Description:Significant higher expression levels of the studied lncRNAs in β-thal patients compared to the controls (all P values < 0.001) were identified.
Causality:No
Causal Description:
Clinical-realted Application: