CBSLR

Summary

CBSLR (CBS mRNA stabilizing lncRNA, HGNC:55459) is a long non-coding RNA gene on chromosome 1q25.3.

Identifiers

Gene identifiers

Field	Value
HGNC ID	HGNC:55459
Approved symbol	CBSLR
Name	CBS mRNA stabilizing lncRNA
Location	1q25.3
Locus type	RNA, long non-coding
Status	Approved
Aliases	TCONS_00001221
Entrez	124904470

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): RS1000014313 (1:185328957 A>G), RS1000050371 (1:185348746 G>C), RS1000054874 (1:185370790 G>T), RS1000085897 (1:185324492 G>A,C), RS1000097683 (1:185369055 G>T), RS1000108379 (1:185323859 G>A), RS1000134683 (1:185376073 A>C,G), RS1000174844 (1:185367708 T>C), RS1000268052 (1:185324173 C>T), RS1000340561 (1:185362967 C>T), RS1000375643 (1:185330938 G>A), RS1000403606 (1:185319588 GTTTTA>G), RS1000490079 (1:185338780 T>A), RS1000537537 (1:185359190 G>A), RS1000637590 (1:185369409 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.