SNORD145

Summary

SNORD145 (small nucleolar RNA, C/D box 145, HGNC:51859) is a gene on chromosome 1p34.1.

Identifiers

Gene identifiers

Field	Value
HGNC ID	HGNC:51859
Approved symbol	SNORD145
Name	small nucleolar RNA, C/D box 145
Location	1p34.1
Locus type	RNA, small nucleolar
Status	Approved
Entrez	109623472
RNAcentral	URS0000ABD825 — snoRNA, 100 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): RS1000710618 (1:44670694 G>A), RS1003325104 (1:44672512 G>A,T), RS1003397955 (1:44671092 G>A), RS1003620287 (1:44672736 C>T), RS1004578917 (1:44671907 C>A,T), RS1006283122 (1:44671744 T>C), RS1006399232 (1:44671448 G>A,C), RS1008137683 (1:44672330 G>A,C), RS1008897583 (1:44670786 A>G), RS1010183228 (1:44670769 A>G), RS1010951499 (1:44670806 T>C), RS1012102833 (1:44672792 G>A), RS1012707712 (1:44671294 T>G), RS1014038565 (1:44671877 T>TTCA), RS1016419962 (1:44671484 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.