SCARNA26B

Summary

SCARNA26B (small Cajal body-specific RNA 26B, HGNC:51394) is a gene on chromosome 1q22.

Identifiers

Gene identifiers

Field	Value
HGNC ID	HGNC:51394
Approved symbol	SCARNA26B
Name	small Cajal body-specific RNA 26B
Location	1q22
Locus type	RNA, small nucleolar
Status	Approved
Entrez	106633816

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): RS1002481432 (1:155784661 C>A,T), RS1006008719 (1:155785209 A>T), RS1006166351 (1:155783772 C>A,T), RS1006375568 (1:155784751 C>A,T), RS1006808255 (1:155785573 A>G), RS1007330016 (1:155783238 T>C), RS1007402149 (1:155785194 T>C), RS1010159783 (1:155785596 C>T), RS1010922011 (1:155784428 C>T), RS1017534991 (1:155784197 C>T), RS1017763666 (1:155785215 A>G,T), RS1018703660 (1:155784658 A>C), RS1022533619 (1:155784052 T>C), RS1022695643 (1:155784442 G>A,T), RS1023598795 (1:155783767 T>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.