BMNCR

Summary

BMNCR (bone marrow associated non-coding RNA, HGNC:54188) is a long non-coding RNA gene on chromosome 1q32.1.

Identifiers

Gene identifiers

Field	Value
HGNC ID	HGNC:54188
Approved symbol	BMNCR
Name	bone marrow associated non-coding RNA
Location	1q32.1
Locus type	RNA, long non-coding
Status	Approved
OMIM	618553
Entrez	107985249

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

Literature-anchored findings (GeneRIF, showing 1)

• LncRNA Bmncr alleviates the progression of osteoporosis by inhibiting RANML-induced osteoclast differentiation. (PMID:31773670)

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): RS1000380902 (1:203407712 C>A), RS1001061138 (1:203405824 C>G,T), RS1002572221 (1:203406210 G>T), RS1002673739 (1:203406779 T>C), RS1002722485 (1:203409106 G>A), RS1003158573 (1:203407687 T>C,G), RS1003517219 (1:203408026 A>G,T), RS1003620326 (1:203407485 T>C), RS1003728077 (1:203405099 C>A,T), RS1004623669 (1:203408073 C>A), RS1005093740 (1:203408210 C>T), RS1005451187 (1:203408403 A>G), RS1006513971 (1:203404622 C>T), RS1006620061 (1:203409522 C>T), RS1006729353 (1:203404657 T>C)

Disease associations

OMIM: gene MIM:618553 | 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.