SNORD148

Summary

SNORD148 (small nucleolar RNA, C/D box 148, HGNC:51862) is a gene on chromosome 16q11.2.

Identifiers

Gene identifiers

Field	Value
HGNC ID	HGNC:51862
Approved symbol	SNORD148
Name	small nucleolar RNA, C/D box 148
Location	16q11.2
Locus type	RNA, small nucleolar
Status	Approved
Entrez	109623466
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): RS1000255983 (16:46886221 A>G), RS1000596457 (16:46886925 G>A,T), RS1001936872 (16:46887795 G>A), RS1004830853 (16:46888461 C>T), RS1004902440 (16:46886708 G>C), RS1007169692 (16:46887101 T>C,G), RS1007843292 (16:46887416 C>G,T), RS1008398324 (16:46887859 C>G,T), RS1009405110 (16:46886312 T>G), RS1010190122 (16:46886193 C>A,T), RS1012089851 (16:46888050 T>G), RS1013730161 (16:46887163 C>T), RS1014321383 (16:46886674 G>T), RS1014427410 (16:46886409 C>T), RS1016966322 (16:46886494 A>G,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.