SNHG34

Summary

SNHG34 (small nucleolar RNA host gene 34, HGNC:59196) is a long non-coding RNA gene on chromosome 7p14.1.

Identifiers

Gene identifiers

Field	Value
HGNC ID	HGNC:59196
Approved symbol	SNHG34
Name	small nucleolar RNA host gene 34
Location	7p14.1
Locus type	RNA, long non-coding
Status	Approved
Entrez	105375239

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): RS1000284102 (7:39330852 C>T), RS1000406208 (7:39336582 G>C), RS1000437442 (7:39336751 T>G), RS1000473590 (7:39330257 T>C), RS1000501636 (7:39332072 C>T), RS1000570732 (7:39330521 C>A), RS1000737916 (7:39338015 A>G), RS1001296361 (7:39327080 C>G), RS1001322118 (7:39332937 T>C), RS1001421361 (7:39333318 C>G,T), RS1001765664 (7:39340094 AG>A), RS1002204563 (7:39333611 G>A,C), RS1002416042 (7:39339517 T>A), RS1002427933 (7:39333166 T>G), RS1002438566 (7:39339724 C>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.