EXOC1L-AS1

Summary

EXOC1L-AS1 (EXOC1L antisense RNA 1, HGNC:58792) is a long non-coding RNA gene on chromosome 4q12.

Identifiers

Gene identifiers

Field	Value
HGNC ID	HGNC:58792
Approved symbol	EXOC1L-AS1
Name	EXOC1L antisense RNA 1
Location	4q12
Locus type	RNA, long non-coding
Status	Approved
Entrez	105377661

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): RS1000120129 (4:55825450 A>T), RS1000712872 (4:55820916 G>A), RS1001025264 (4:55820805 C>T), RS10014844 (4:55826665 T>A), RS1002181557 (4:55823771 C>A,T), RS1002845314 (4:55820930 G>T), RS1002860412 (4:55822720 A>G), RS1003470918 (4:55822636 T>C,G), RS1003898078 (4:55826201 A>G,T), RS1003954972 (4:55825951 G>C), RS1004188501 (4:55823855 T>G), RS1004786798 (4:55823474 A>T), RS1005198817 (4:55825324 A>C), RS1005790942 (4:55825004 G>A), RS1006246727 (4:55824665 G>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.