SNORD144

Summary

SNORD144 (small nucleolar RNA, C/D box 144, HGNC:50401) is a gene on chromosome 4q21.22.

Identifiers

Gene identifiers

Field	Value
HGNC ID	HGNC:50401
Approved symbol	SNORD144
Name	small nucleolar RNA, C/D box 144
Location	4q21.22
Locus type	RNA, small nucleolar
Status	Approved
Aliases	ZL6
Entrez	106633809
RNAcentral	URS0000A76DCB — snoRNA, 86 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): RS1000154176 (4:82899867 A>C), RS1001156375 (4:82898420 G>A), RS1002370516 (4:82899431 T>C), RS1003385087 (4:82899284 C>T), RS1004959006 (4:82898055 T>C,G), RS1005175230 (4:82898046 C>A,G,T), RS1005284988 (4:82898384 T>C), RS1011632294 (4:82898937 G>A), RS1013872530 (4:82899189 C>T), RS1014215997 (4:82898967 C>T), RS1015278960 (4:82899481 T>C), RS1015413237 (4:82899269 T>C), RS1016243224 (4:82899725 C>A), RS1016464403 (4:82899364 G>C), RS1016575762 (4:82898088 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.