SNORD142

Summary

SNORD142 (small nucleolar RNA, C/D box 142, HGNC:50389) is a gene on chromosome 10p15.2.

Identifiers

Gene identifiers

Field	Value
HGNC ID	HGNC:50389
Approved symbol	SNORD142
Name	small nucleolar RNA, C/D box 142
Location	10p15.2
Locus type	RNA, small nucleolar
Status	Approved
Aliases	ZL68
Entrez	106633806
RNAcentral	URS0000A766EB — snoRNA, 195 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): RS1000371409 (10:3132672 C>A,T), RS1000425293 (10:3132537 C>A,T), RS1001736812 (10:3132157 G>A), RS1003815709 (10:3134143 T>C), RS1004168134 (10:3134340 G>A,C,T), RS1005105870 (10:3134508 G>A,C), RS1005767705 (10:3133101 T>C,G), RS1007012861 (10:3134608 C>G,T), RS1008276065 (10:3133577 C>G,T), RS1008359945 (10:3134026 G>A), RS1008946943 (10:3134738 C>T), RS1011565424 (10:3133470 G>A), RS1011734088 (10:3132278 T>C), RS1012516911 (10:3134328 A>C), RS1012862962 (10:3134106 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.