circRNA basic information
circBase ID: -
Name: hsa_circ_RHBDD1
Synonym: hsa_circ_102927
Host Gene: RHBDD1
Genomic location(hg19): -
Genomic location(hg38): -
Subcellular localization: not tested
 
 
 
 
 
 
 
Disease basic information
MONDO ID:
0021178
MONDO name: injury
Disease details: traumatic lung injury
Disease DO ID:
-
Disease MeSH ID:
D014947
Disease NCIt ID:
C3671
Disease ICD11 ID:
-
Disease OMIM ID:
-
Species: Human
Species details: Homo sapiens
Tissue specimen:

plasma

Cell lines:

-

In vivo animal model:

-

circRNA-disease information
Expression pattern:
DN
Associated gene: -
Associated microRNA: -
Biological function: May serve a role in the development/pathophysiology of traumatic lung injury and has potential diagnostic biomarker value.
Molecular mechanism: Bioinformatically predicted ceRNA network (circRNA-miRNA-mRNA) based on the validated circRNAs; specific miRNA/mRNA pairs for this circRNA not specified in the provided text.
Biological pathway or process:

ceRNA regulation (other); PI3K/AKT/mTOR (other); other pathway/process (other)

Detected method:
Q
M
Validation methods:

Microarray; RT-qPCR; RNase R Treatment; Clinical Sample Validation; ROC Analysis; Bioinformatics Analysis

Clinical significance:

ROC analysis showed hsa_circ_102927 could distinguish TLI plasma from normal controls (AUC 0.978; specificity 95.0%; sensitivity 95.0%).

Description:

hsa_circRNA_102927 (host gene RHBDD1) is down-regulated in plasma from traumatic lung injury patients and shows strong diagnostic discrimination by ROC analysis. The study further places it within a predicted ceRNA (circRNA-miRNA-mRNA) network potentially relevant to TLI pathophysiology.

Confidence score:

0.5963

Other information
Title:

Microarray and bioinformatics analysis of circular RNAs expression profile in traumatic lung injury.

Journal: Experimental and therapeutic medicine
Published: 2020
PubMed ID: 32509009
Study type:

combined biological and clinical study

Data availability: The datasets used and/or analyzed during the present study are available from the corresponding author on reasonable request.
Code availability: -