Entry Detail

General Information

Database ID: LDA0016327
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:LINC00467
Full Name:long intergenic non-protein coding RNA 467
Category:LncRNA
Species:Homo sapiens
Synonyms:ASAP|C1orf97
Chromosome:1
Strand:+
Coordinate:
Start Site(bp):211382755End Site(bp):211432535
External Links:
Ensembl ID:ENSG00000153363
Ensembl Transcript ID:N/A
Entrez Gene:84791.0
NONCODE ID:N/A
RefSeq Accession:N/A

 

ncRNA Association Statistics

Total Associated Disease Number:26   
More Information
Causal Disease Number:24
Network:
Top Causal Diseases:
Carcinoma, Hepatocellular  (Score: 1)
Carcinoma, Hepatocellular  (Score: 1)
Adenocarcinoma of Lung  (Score: 0.999893)
Adenocarcinoma of Lung  (Score: 0.999893)
Glioma  (Score: 0.999893)
Glioma  (Score: 0.999893)
Leukemia, Myeloid, Acute  (Score: 0.985791)
Colorectal Neoplasms  (Score: 0.985791)
Esophageal Squamous Cell Carcinoma  (Score: 0.985791)
Leukemia, Myeloid, Acute  (Score: 0.985791)
More Information

 

 

Disease Information

 Disease OntologyMeSH
Disease ID:DOID:12297
Disease Name:Vogt-Koyanagi-Harada disease
Category:Disease Ontology
Type:Eye Diseases
Define:An autoimmune disease that is caused by T helper cell mediated autoimmune attack of melanocytes resulting in inflammation of the inside of the eye, whitening of hair, skin pigment loss, and meningitis.
Alias:Harada's disease//Vogt-Koyanagi syndrome//uveomeningoencephalitic syndrome

 

Disease Association Statistics

Total Associated ncRNA Number:2   
More Information
Causal ncRNA Number:0
Network:
Top Causal ncRNAs:
More Information

 

Evidence Support

Strong Evidence:Genotyping//FISH//qRT-PCR//Cell Proliferation Assay//ELISA
Weak Evidence:

 

Reference

[1] PubMed ID:32400232
Disease Name:Vogt-Koyanagi-Harada disease
Sample:
Dysfunction Pattern:Mutation(Rs12569232)
Validated Method:Genotyping//FISH//qRT-PCR//Cell Proliferation Assay//ELISA
Description:The rs12569232 was associated with the expression of linc00467. The expression of linc00467 was up-regulated in PBMCs and CD4+T cells from VKH disease and BD patients.
Causality:No
Causal Description:
Clinical-realted Application: