Entry Detail


General Information

Database ID: LDA0016513
Species: Homo sapiens
Confidence Score: 0.548294
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:KRT88P
Full Name:keratin 88, pseudogene
Category:LncRNA
Species:Homo sapiens
Synonyms:HBC|KRT122P|KRTHBP3
Chromosome:12
Strand:+
Coordinate:
Start Site(bp):52263781End Site(bp):52268497
External Links:
Ensembl ID:ENSG00000284883
Ensembl Transcript ID:N/A
Entrez Gene:85348.0
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:0060224D001281
Disease Name:atrial fibrillationAtrial Fibrillation
Category:Disease OntologyMeSH
Type:Cardiovascular Diseases
Define:A heart conduction disease that is characterized by uncoordinated electrical activity in the heart's upper chambers (the atria), which causes the heartbeat to become fast and irregular and has symptoms palpitations, weakness, fatigue, lightheadedness, dizziness, confusion, shortness of breath and chest pain.Abnormal cardiac rhythm that is characterized by rapid, uncoordinated firing of electrical impulses in the upper chambers of the heart (HEART ATRIA). In such case, blood cannot be effectively pumped into the lower chambers of the heart (HEART VENTRICLES). It is caused by abnormal impulse generation.
Alias:A-fibAtrial Fibrillation//Atrial Fibrillations//Fibrillation, Atrial//Fibrillations, Atrial//Auricular Fibrillation//Auricular Fibrillations//Fibrillation, Auricular//Fibrillations, Auricular//Persistent Atrial Fibrillation//Atrial Fibrillation, Persistent//Atrial Fibrillations, Persistent//Fibrillation, Persistent Atrial//Fibrillations, Persistent Atrial//Persistent Atrial Fibrillations//Familial Atrial Fibrillation//Atrial Fibrillation, Familial//Atrial Fibrillations, Familial//Familial Atrial Fibrillations//Fibrillation, Familial Atrial//Fibrillations, Familial Atrial//Paroxysmal Atrial Fibrillation//Atrial Fibrillation, Paroxysmal//Atrial Fibrillations, Paroxysmal//Fibrillation, Paroxysmal Atrial//Fibrillations, Paroxysmal Atrial//Paroxysmal Atrial Fibrillations

 

Disease Association Statistics

Total Associated ncRNA Number:1718   
More Information
Causal ncRNA Number:0
Network:
Top Causal ncRNAs:
More Information

 

Evidence Support

Strong Evidence:
Weak Evidence:RNA-seq

 

Reference

[1] PubMed ID:31843366
Disease Name:Atrial Fibrillation
Sample:AF tissues and matched controls
Dysfunction Pattern:Expression[lower expressed]
Validated Method:RNA-seq
Description:Among the 557 lncRNAs, 30 and 837 were up-regulated and down-regulated in AF patients compared with controls, respectively.
Causality:No
Causal Description:
Clinical-realted Application: