Entry Detail

General Information

Database ID: LDA0016362
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:IPW
Full Name:imprinted in Prader-Willi syndrome
Category:LncRNA
Species:Homo sapiens
Synonyms:NCRNA00002
Chromosome:15
Strand:+
Coordinate:
Start Site(bp):25116545End Site(bp):25122476
External Links:
Ensembl ID:N/A
Ensembl Transcript ID:N/A
Entrez Gene:3653.0
NONCODE ID:N/A
RefSeq Accession:N/A

 

ncRNA Association Statistics

Total Associated Disease Number:4   
More Information
Causal Disease Number:2
Network:
Top Causal Diseases:
Carcinoma, Ductal  (Score: 0.731059)
Carcinoma, Ductal  (Score: 0.731059)
More Information

 

 

Disease Information

 Disease OntologyMeSH
Disease ID:C536914
Disease Name:Thyroid cancer, medullary
Category:MeSH
Type:Neoplasms
Define:A neuroendocrine carcinoma that originates in the C-cells of the THYROID GLAND; about 10-20% of cases are familial. It occurs sporadically or is associated with MULTIPLE ENDOCRINE NEOPLASIA SYNDROMES. Germline and somatic mutations in RET and NTRK1 genes have been identified. OMIM: 155240
Alias:

 

Disease Association Statistics

Total Associated ncRNA Number:8   
More Information
Causal ncRNA Number:0
Network:
Top Causal ncRNAs:
More Information

 

Evidence Support

Strong Evidence:qRT-PCR
Weak Evidence:

 

Reference

[1] PubMed ID:33407723
Disease Name:Thyroid cancer, medullary
Sample:medullary thyroid tumor tissues
Dysfunction Pattern:Expression [highly expressed]
Validated Method:qRT-PCR
Description:Here we have tested three up-regulated (RMST, FTX, IPW) and one down-regulated (RMRP) lncRNAs in our samples (formalin fixed paraffin embedded tissues from twenty-one MEN2 and ten sMTC patients) by RT-qPCR analysis.
Causality:No
Causal Description:
Clinical-realted Application: