MIR550A3HG

Summary

MIR550A3HG (MIR550A3 host gene, HGNC:58072) is a long non-coding RNA gene on chromosome 7p14.3.

At a glance

• Clinical variants (ClinVar): 11 total

Identifiers

Gene identifiers

Field	Value
HGNC ID	HGNC:58072
Approved symbol	MIR550A3HG
Name	MIR550A3 host gene
Location	7p14.3
Locus type	RNA, long non-coding
Status	Approved
Ensembl gene	ENSG00000293330
Entrez	646762
RNAcentral	URS000075E4C4 — lncRNA, 5784 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

11 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): RS1000129721 (7:29654838 A>C), RS1000314433 (7:29667047 T>C), RS1000321750 (7:29672754 C>T), RS1000369660 (7:29660741 G>A), RS1000471470 (7:29649240 A>T), RS1000561299 (7:29685045 G>A,C), RS1000614922 (7:29673059 T>C), RS1000718257 (7:29678974 A>G), RS1000895438 (7:29655799 A>G), RS1000973189 (7:29662209 A>G), RS1001110796 (7:29651326 A>C), RS1001183054 (7:29685186 C>G,T), RS1001262785 (7:29665991 G>A), RS1001314997 (7:29666304 C>T), RS1001320568 (7:29661962 A>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

Clinical trials (associated diseases)

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