GRSF1-AS1

Summary

GRSF1-AS1 (GRSF1 antisense RNA 1, HGNC:58807) is a long non-coding RNA gene on chromosome 4q13.3.

Identifiers

Gene identifiers

Field	Value
HGNC ID	HGNC:58807
Approved symbol	GRSF1-AS1
Name	GRSF1 antisense RNA 1
Location	4q13.3
Locus type	RNA, long non-coding
Status	Approved
Entrez	124900710

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): RS1000001056 (4:70847689 T>A), RS1000474184 (4:70847139 A>G), RS1000983011 (4:70840572 G>T), RS1001127305 (4:70840686 C>A), RS1001351866 (4:70840399 G>A), RS1001538830 (4:70838497 T>C), RS10017438 (4:70845228 G>A,T), RS1001787180 (4:70843813 G>A), RS10018128 (4:70847324 C>G,T), RS1002227862 (4:70839931 T>A,C,G), RS1002238013 (4:70837209 TTAGTAAGAATCC>T), RS1002239826 (4:70846779 C>T), RS1002270878 (4:70847011 G>A,T), RS1002393124 (4:70842229 G>T), RS1002514589 (4:70839141 G>A)

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.