SNORD147

Summary

SNORD147 (small nucleolar RNA, C/D box 147, HGNC:51861) is a gene on chromosome 11p15.1.

Identifiers

Gene identifiers

Field	Value
HGNC ID	HGNC:51861
Approved symbol	SNORD147
Name	small nucleolar RNA, C/D box 147
Location	11p15.1
Locus type	RNA, small nucleolar
Status	Approved
Entrez	109623465
RNAcentral	URS0000ABD896 — snoRNA, 85 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): RS1000635753 (11:16925875 T>C,G), RS1000919563 (11:16926063 C>T), RS1002324634 (11:16926176 G>C), RS1003733024 (11:16927617 A>G), RS1006577741 (11:16925585 G>A), RS1006916448 (11:16926580 T>C), RS1007637208 (11:16925569 C>A), RS1008948448 (11:16927116 A>G), RS1009420975 (11:16927231 A>G), RS1011966758 (11:16927558 A>C,G), RS1012346830 (11:16927139 G>A,T), RS1016733452 (11:16927625 G>T), RS1016746026 (11:16926179 T>C), RS1017850820 (11:16926616 G>C), RS1018153934 (11:16926284 T>A)

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.