Entry Detail

General Information

Database ID: LDA0015278
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:LOC338963
Full Name:-
Category:LncRNA
Species:Homo sapiens
Synonyms:-
Chromosome:15
Strand:-
Coordinate:
Start Site(bp):82710471End Site(bp):82713993
External Links:
Ensembl ID:N/A
Ensembl Transcript ID:N/A
Entrez Gene:338963.0
NONCODE ID:N/A
RefSeq Accession:N/A

 

ncRNA Association Statistics

Total Associated Disease Number:2   
More Information
Causal Disease Number:0
Network:
Top Causal Diseases:
More Information

 

 

Disease Information

 Disease OntologyMeSH
Disease ID:DOID:0050214
Disease Name:Lambert-Eaton myasthenic syndrome
Category:Disease Ontology
Type:Nervous System Diseases
Define:A neuromuscular junction disease that is characterized by an abnormality of acetylcholine (ACh) release at the neuromuscular junction which results from an autoimmune attack against voltage-gated calcium channels (VGCC) on the presynaptic motor nerve terminal.
Alias:Eaton-Lambert syndrome//LEMS//Lambert-Eaton 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:qRT-PCR
Weak Evidence:

 

Reference

[1] PubMed ID:35508598
Disease Name:Lambert-Eaton myasthenic syndrome
Sample:three LEMS patients
Dysfunction Pattern:Expression(highly expressed)
Validated Method:qRT-PCR
Description:Among these, lncRNA LOC338963 and its neighboring mRNA AP3B2 were upregulated jointly, which was confirmed by qRT-PCR.
Causality:No
Causal Description:
Clinical-realted Application: