circRNA basic information
circBase ID: -
Name: hsa_circ_TADA2A
Synonym: hsa_circRNA_102049 / circRNA_102049
Host Gene: TADA2A
Genomic location(hg19): -
Genomic location(hg38): -
Subcellular localization: not tested
 
 
 
 
 
 
 
Disease basic information
MONDO ID:
0004975
MONDO name: Alzheimer disease
Disease details: Alzheimer's disease / AD
Disease DO ID:
10652
Disease MeSH ID:
D000544
Disease NCIt ID:
C2866
Disease ICD11 ID:
1611724421
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: hsa-miR-197-5p, hsa-miR-6871-5p, hsa-miR-6751-5p, hsa-miR-6803-5p, hsa-miR-194-3p
Biological function: Potential plasma biomarker; down-regulated in AD (not significantly changed in MCI).
Molecular mechanism: Predicted circRNA-miRNA-mRNA regulatory network and enrichment analyses; no experimental validation of specific interactions reported.
Biological pathway or process:

ceRNA regulation (other); other pathway/process (other)

Detected method:
Q
M
Validation methods:

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

Clinical significance:

ROC analysis showed good diagnostic accuracy for distinguishing AD from healthy controls (AUC 0.829).

Description:

hsa_circRNA_102049 (TADA2A locus) is decreased in plasma of AD patients compared with healthy controls and does not show AD-like upregulation in MCI. The study supports its diagnostic potential via ROC analysis and suggests a predicted circRNA-miRNA-mRNA regulatory role based on bioinformatic analyses.

Confidence score:

0.5963

Other information
Title:

A Plasma Circular RNA Profile Differentiates Subjects with Alzheimer's Disease and Mild Cognitive Impairment from Healthy Controls.

Journal: International journal of molecular sciences
Published: 2022
PubMed ID: 36362022
Study type:

combined biological and clinical study

Data availability: The dataset generated during the current study will be available from the corresponding author (P.P.) upon reasonable request.
Code availability: -