SCARNA26A

Summary

SCARNA26A (small Cajal body-specific RNA 26A, HGNC:50385) is a gene on chromosome 1q22.

At a glance

• Clinical variants (ClinVar): 1 total

Identifiers

Gene identifiers

Field	Value
HGNC ID	HGNC:50385
Approved symbol	SCARNA26A
Name	small Cajal body-specific RNA 26A
Location	1q22
Locus type	RNA, small nucleolar
Status	Approved
Entrez	106633810
RNAcentral	URS00008E3A3C — ncRNA, 148 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

1 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): RS1003715969 (1:155680062 A>G), RS1004110839 (1:155679811 G>A,C,T), RS1004162396 (1:155681017 A>G), RS1004430794 (1:155680669 C>A,T), RS1004675689 (1:155678670 C>T), RS1007244857 (1:155680670 G>A), RS1008218911 (1:155678758 A>AT), RS1008353307 (1:155678650 G>T), RS1011431554 (1:155681059 T>C), RS1012529687 (1:155679674 C>T), RS1012836827 (1:155680635 C>G,T), RS1012866264 (1:155680086 A>G), RS1014633424 (1:155679827 CA>C), RS1015441521 (1:155680707 C>G,T), RS1015826369 (1:155681020 G>A)

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.