Entry Detail

General Information

Database ID: LDA0016287
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: Yes

 


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:LINC01102
Full Name:N/A
Category:LncRNA
Species:Homo sapiens
Synonyms:N/A
Chromosome:N/A
Strand:N/A
Coordinate:
Start Site(bp):0End Site(bp):0
External Links:
Ensembl ID:N/A
Ensembl Transcript ID:N/A
Entrez Gene:N/A
NONCODE ID:N/A
RefSeq Accession:NR_015399.1

 

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:6367
Disease Name:acral lentiginous melanoma
Category:Disease Ontology
Type:Neoplasms
Define:A skin melanoma that is characterized by slow growth of a small pigmented spot on the skin with a clearly defined edge, surrounded by normal-appearing skin and occurs on occurs on non hair-bairing surfaces including hands and feet, subungual sites, and fingers or toes.
Alias:acral lentiginous melanoma, malignant//malignant acral lentiginous melanoma

 

Disease Association Statistics

Total Associated ncRNA Number:20   
More Information
Causal ncRNA Number:0
Network:
Top Causal ncRNAs:
More Information

 

Evidence Support

Strong Evidence:qRT-PCR
Weak Evidence:

 

Reference

[1] PubMed ID:31966073
Disease Name:acral lentiginous melanoma
Sample:tumor and six adjacent non-tumor tissues
Dysfunction Pattern:Expression[highly expressed]
Validated Method:qRT-PCR//Microarray
Description:The top 5 upregulated lncRNAs were T380070, ENST00000554431, T097678, GSE61474_TCONS_00183926 and NR_015403.
Causality:No
Causal Description:
Clinical-realted Application: