circRNA basic information
circBase ID: -
Name: hsa_circ_NRIP1
Synonym: circular NRIP1
Host Gene: NRIP1
Genomic location(hg19): -
Genomic location(hg38): -
Subcellular localization: extracellular
 
 
 
 
 
 
 
Disease basic information
MONDO ID:
0005081
MONDO name: preeclampsia
Disease details: pre-eclampsia
Disease DO ID:
10591
Disease MeSH ID:
D011225
Disease NCIt ID:
C85021
Disease ICD11 ID:
229121159
Disease OMIM ID:
-
Species: Human
Species details: Homo sapiens
Tissue specimen:

plasma

Cell lines:

-

In vivo animal model:

-

circRNA-disease information
Expression pattern:
DS
Associated gene: -
Associated microRNA: -
Biological function: Permits discrimination between pre-eclampsia and trisomy 21 by comparing relative quantities of linear versus circular NRIP1 in first trimester plasma.
Molecular mechanism: Relative abundance shift between linear NRIP1 and circular NRIP1 in pre-eclampsia; no mechanistic (e.g., ceRNA/protein binding) experiments reported.
Biological pathway or process:

not specified

Detected method:
Q
Validation methods:

RT-qPCR; Sanger Sequencing; Clinical Sample Validation

Clinical significance:

Quantitative assays discriminating linear and circular NRIP1 enable presymptomatic screening of pre-eclampsia and discrimination from trisomy 21.

Description:

This study detected and quantified circular NRIP1 in first-trimester maternal plasma and used the relative balance between linear and circular NRIP1 to help discriminate pre-eclampsia from trisomy 21 in presymptomatic screening. No downstream miRNA/protein/pathway mechanism for circNRIP1 was experimentally established in this paper.

Confidence score:

0.429

Other information
Title:

The bivariate NRIP1/ZEB2 RNA marker permits non-invasive presymptomatic screening of pre-eclampsia.

Journal: Scientific reports
Published: 2020
PubMed ID: 33318568
Study type:

combined biological and clinical study

Data availability: NCBI SRA, accession SUB7550002
Code availability: https://github.com/qinzhu/VERSE; https://github.com/MyronBest/thromboSeq_source_code