MIR381HG

Summary

MIR381HG (MIR381 host gene, HGNC:20136) is a long non-coding RNA gene on chromosome 14q32.31.

Identifiers

Gene identifiers

Field	Value
HGNC ID	HGNC:20136
Approved symbol	MIR381HG
Name	MIR381 host gene
Location	14q32.31
Locus type	RNA, long non-coding
Status	Approved
Aliases	NCRNA00225
Entrez	378881
RNAcentral	URS00001E5E1D — lncRNA, 425 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: 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): RS1000110976 (14:101049759 G>A), RS1000145018 (14:101051981 C>A,G), RS1000942364 (14:101046276 G>A), RS1001152112 (14:101050304 G>C), RS1001499669 (14:101048356 A>G), RS1001554749 (14:101051043 C>A), RS1002019997 (14:101043865 G>T), RS1002100659 (14:101051658 T>C), RS1002153173 (14:101051448 C>A,T), RS1002444581 (14:101046676 T>C), RS1002474296 (14:101043693 G>A,T), RS1002539468 (14:101044069 G>A), RS1002583356 (14:101045115 G>A), RS1003276587 (14:101049769 G>C), RS1003662338 (14:101045775 T>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: 1 entry (VIP=true, CPIC=false)

Clinical trials (associated diseases)

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