MYOSLID-AS1

Summary

MYOSLID-AS1 (MYOSLID antisense RNA 1, HGNC:54063) is a long non-coding RNA gene on chromosome 2q33.3.

Identifiers

Gene identifiers

Field	Value
HGNC ID	HGNC:54063
Approved symbol	MYOSLID-AS1
Name	MYOSLID antisense RNA 1
Location	2q33.3
Locus type	RNA, long non-coding
Status	Approved
Entrez	101927865
RNAcentral	URS000075CD7A — lncRNA, 601 nt, 1 organism(s)

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: 16 (showing top): CBX7_TARGET_GENES, FOXN3_TARGET_GENES, HOXB4_TARGET_GENES, PIAS4_TARGET_GENES, SOX11_TARGET_GENES, ZNF597_TARGET_GENES, ZNF766_TARGET_GENES, SAFB2_TARGET_GENES, POU2AF1_TARGET_GENES, DESCARTES_FETAL_MUSCLE_MYELOID_CELLS, RAG1_TARGET_GENES, BRCA2_TARGET_GENES, ZBED5_TARGET_GENES, ZNF224_TARGET_GENES, NOTCH3_TARGET_GENES

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): RS1000037600 (2:207224014 G>A), RS1000157732 (2:207194232 G>A,C), RS1000167451 (2:207205036 T>C), RS1000207581 (2:207250142 G>A), RS1000209733 (2:207194580 A>G), RS1000266583 (2:207228637 A>G), RS1000273665 (2:207235214 A>C,G), RS1000277454 (2:207197578 T>A), RS1000307025 (2:207186918 C>A,G), RS1000383399 (2:207250146 C>T), RS1000403843 (2:207187226 T>C), RS1000494248 (2:207224302 A>C), RS1000545365 (2:207192903 G>A,T), RS1000595823 (2:207241618 T>C,G), RS1000633011 (2:207197202 T>A,C,G)

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

CTD chemical–gene interactions

1 total (human), top 1 by PubMed support.

Chemical	Actions (top 5)	PubMed papers
Smoke	decreases expression	1

Clinical trials (associated diseases)

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