COL25A1-AS1

Summary

COL25A1-AS1 (COL25A1 antisense RNA 1, HGNC:58867) is a long non-coding RNA gene on chromosome 4q25.

Identifiers

Gene identifiers

Field	Value
HGNC ID	HGNC:58867
Approved symbol	COL25A1-AS1
Name	COL25A1 antisense RNA 1
Location	4q25
Locus type	RNA, long non-coding
Status	Approved
Entrez	124900756

Gene structure

Transcript identifiers

Ensembl transcripts: 0

RefSeq mRNA: 0 — MANE Select: None

Canonical transcript exons

None — 0 exons

Expression profiles

Top tissues by expression

0 total, by Bgee expression score (0-100, higher = more expressed):

Regulation

Is transcription factor: no

Cross-species orthologs

0 orthologs

Protein

Protein identifiers

Canonical reviewed UniProt: None (reviewed: )

All UniProt accessions (0):

RefSeq proteins (0): (*=MANE)

Domains & families (InterPro)

Structure

Experimental structures (PDB)

0 structures.

Predicted structure (AlphaFold)

Function

Pathways and Gene Ontology

Reactome pathways

0 pathways

MSigDB gene sets: 0 (showing top):

GO Biological Process (0):

GO Molecular Function (0):

GO Cellular Component (0):

Protein interactions and networks

STRING

0 interactions, top by confidence (×1000):

IntAct

0 interactions, top by confidence:

SIGNOR signaling

0 interactions.

Disease & clinical

Clinical variants and AI predictions

ClinVar

0 variants total. Per-class counts are floors (≥ shown; pagination cap):

Classification	Count (floor)
Pathogenic	0
Likely pathogenic	0
Uncertain significance	0
Likely benign	0
Benign	0

Top pathogenic / likely-pathogenic (0)

SpliceAI

0 predictions. Top by Δscore:

AlphaMissense

0 scored. Top likely-pathogenic:

dbSNP variants (sampled 300 via entrez): RS1000141116 (4:109022412 A>G), RS1000336937 (4:109027919 C>T), RS1000353740 (4:109026385 G>C), RS1000367917 (4:109044094 T>A,C), RS1000385026 (4:109026206 G>A,T), RS1000403076 (4:109046853 A>G), RS1000638234 (4:109039687 C>T), RS1000680964 (4:109025007 C>A,T), RS1000721598 (4:109024695 A>G), RS1000747076 (4:109032947 T>C), RS1000945250 (4:109026408 T>A,C), RS1000966233 (4:109039998 G>A), RS1001075216 (4:109037695 G>A), RS1001231227 (4:109029635 G>C), RS10012573 (4:109027430 A>C,T)

Disease associations

OMIM: gene `` | disease phenotypes:

GenCC curated gene-disease

Mondo (0):

Orphanet (0):

HPO phenotypes

0 total (0 of 0 shown, HPO-id order):

GWAS associations

0 associations (top):

Drugs & pharmacology

Drug and pharmacology data

Is drug target: no

PharmGKB: 0 entries

Clinical trials (associated diseases)

0 trials via MONDO — disease-level, not drug-specific.