Entry Detail

General Information

Database ID: LDA0016994
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:MALAT1
Full Name:metastasis associated lung adenocarcinoma transcript 1
Category:LncRNA
Species:Homo sapiens
Synonyms:HCN|LINC00047|NCRNA00047|NEAT2|PRO2853
Chromosome:11
Strand:+
Coordinate:
Start Site(bp):65497738End Site(bp):65506516
External Links:
Ensembl ID:ENSG00000251562
Ensembl Transcript ID:N/A
Entrez Gene:378938.0
NONCODE ID:N/A
RefSeq Accession:NR_002819.4

 

ncRNA Association Statistics

Total Associated Disease Number:204   
More Information
Causal Disease Number:132
Network:
Top Causal Diseases:
Breast Neoplasms  (Score: 1)
Breast Neoplasms  (Score: 1)
Coronary Artery Disease  (Score: 1)
Stomach Neoplasms  (Score: 1)
Colorectal Neoplasms  (Score: 1)
tongue squamous cell carcinoma  (Score: 1)
Colorectal Neoplasms  (Score: 1)
Stomach Neoplasms  (Score: 1)
Carcinoma, Non-Small-Cell Lung  (Score: 1)
Carcinoma, Renal Cell  (Score: 1)
More Information

 

 

Disease Information

 Disease OntologyMeSH
Disease ID:DOID:8924D016553
Disease Name:autoimmune thrombocytopenic purpuraPurpura, Thrombocytopenic, Idiopathic
Category:Disease OntologyMeSH
Type:Hemic and Lymphatic Diseases
Define:A primary thrombocytopenia that involves relatively few platelets in blood as a result of autoantibodies.Thrombocytopenia occurring in the absence of toxic exposure or a disease associated with decreased platelets. It is mediated by immune mechanisms, in most cases IMMUNOGLOBULIN G autoantibodies which attach to platelets and subsequently undergo destruction by macrophages. The disease is seen in acute (affecting children) and chronic (adult) forms.
Alias:Immune thrombocytopenic purpura//idiopathic thrombocytopenic purpura//primary thrombocytopenic purpuraPurpura, Thrombocytopenic, Idiopathic//Idiopathic Thrombocytopenic Purpura//Idiopathic Thrombocytopenic Purpuras//Purpura, Idiopathic Thrombocytopenic//Purpuras, Idiopathic Thrombocytopenic//Thrombocytopenic Purpura, Idiopathic//Thrombocytopenic Purpuras, Idiopathic//Immune Thrombocytopenic Purpura//Immune Thrombocytopenic Purpuras//Purpura, Immune Thrombocytopenic//Purpuras, Immune Thrombocytopenic//Thrombocytopenic Purpura, Immune//Thrombocytopenic Purpuras, Immune//Immune Thrombocytopenia//Immune Thrombocytopenias//Thrombocytopenia, Immune//Thrombocytopenias, Immune//Thrombocytopenic Purpura, Autoimmune//Werlhof Disease//Disease, Werlhof//Werlhof's Disease//Disease, Werlhof's//Werlhofs Disease//Autoimmune Thrombocytopenia//Autoimmune Thrombocytopenias//Thrombocytopenia, Autoimmune//Thrombocytopenias, Autoimmune//Autoimmune Thrombocytopenic Purpura//Autoimmune Thrombocytopenic Purpuras//Purpura, Autoimmune Thrombocytopenic//Purpuras, Autoimmune Thrombocytopenic//Purpura, Thrombocytopenic, Autoimmune

 

Disease Association Statistics

Total Associated ncRNA Number:12   
More Information
Causal ncRNA Number:2
Network:
Top Causal ncRNAs:
PVT1  (Score: 0.731059)
PVT1  (Score: 0.731059)
More Information

 

Evidence Support

Strong Evidence:qRT-PCR
Weak Evidence:

 

Reference

[1] PubMed ID:32563217
Disease Name:Purpura, Thrombocytopenic, Idiopathic
Sample:blood
Dysfunction Pattern:Expression[highly expressed]
Validated Method:qRT-PCR
Description:Both lncRNAs MALAT1 and THRIL were significantly upregulated in ITP patients in comparison to HCs ( p < .0001 and = .001 respectively).
Causality:No
Causal Description:
Clinical-realted Application: