SNORD149

Summary

SNORD149 (small nucleolar RNA, C/D box 149, HGNC:51863) is a gene on chromosome 8q24.3.

Identifiers

Gene identifiers

Field	Value
HGNC ID	HGNC:51863
Approved symbol	SNORD149
Name	small nucleolar RNA, C/D box 149
Location	8q24.3
Locus type	RNA, small nucleolar
Status	Approved
Entrez	109623485
RNAcentral	URS0000ABD85D — snoRNA, 64 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): RS1002362123 (8:143506819 C>A), RS1004094916 (8:143507521 C>T), RS1005901447 (8:143507359 G>C,T), RS1006151169 (8:143505755 G>A), RS1006596858 (8:143506223 C>T), RS1007460052 (8:143508239 G>A), RS1009070982 (8:143506067 C>A,T), RS1009368377 (8:143505919 G>A), RS1009625921 (8:143506998 A>C), RS1009746490 (8:143508140 C>T), RS1009959282 (8:143506921 G>A), RS1010036507 (8:143507908 A>G), RS1013304884 (8:143508000 C>T), RS1013357166 (8:143508162 G>A,C), RS1013737064 (8:143507394 G>A,C)

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.