circRNA basic information
circBase ID: hsa_circ_0000479
Name: hsa_circ_EPSTI1
Synonym: hsa_circRNA_000479
Host Gene: EPSTI1
Genomic location(hg19): chr13:43528083-43544806:-
Genomic location(hg38): chr13:42953947-42970670:-
Subcellular localization: not tested
 
 
 
 
 
 
 
Disease basic information
MONDO ID:
0007915
MONDO name: systemic lupus erythematosus
Disease details: systemic lupus erythematosus / SLE
Disease DO ID:
9074
Disease MeSH ID:
D008180
Disease NCIt ID:
C3201
Disease ICD11 ID:
749596428
Disease OMIM ID:
152700
Species: Human
Species details: Homo sapiens
Tissue specimen:

peripheral blood

Cell lines:

-

In vivo animal model:

-

circRNA-disease information
Expression pattern:
UP
Associated gene: EPSTI1
Associated microRNA: -
Biological function: Associated with laboratory indicators and clinical manifestations in SLE; may be involved in SLE pathogenesis (in neutrophils).
Molecular mechanism: Not experimentally validated in this study; discussion suggests possible ceRNA-related regulation in other contexts.
Biological pathway or process:

immune regulation (other)

Detected method:
Q
Validation methods:

Back-Splice Junction PCR / divergent primers PCR; Sanger Sequencing; RT-qPCR; Clinical Sample Validation

Clinical significance:

Higher neutrophil hsa_circ_0000479 levels are associated with multiple laboratory indicators (NEUT, C3, anti-dsDNA, AnuA) and clinical manifestations (Raynaud’s phenomenon, alopecia, leucopenia) in SLE, suggesting potential clinical value.

Description:

hsa_circ_0000479 (from host gene EPSTI1) is up-regulated in neutrophils from SLE patients versus healthy controls. Its higher neutrophil expression correlates with key laboratory parameters (e.g., lower NEUT and C3; higher anti-dsDNA and anti-nucleosome antibodies) and with Raynaud’s phenomenon, alopecia, and leucopenia, indicating potential involvement in SLE immune dysregulation and possible clinical value.

Confidence score:

0.5129

Other information
Title:

Elevated expression of hsa_circ_0000479 in neutrophils correlates with features of systemic lupus erythematosus.

Journal: Annals of medicine
Published: 2024
PubMed ID: 38300888
Study type:

combined biological and clinical study

Data availability: Data supporting the findings of this study are available from the corresponding author upon reasonable request.
Code availability: -