MALNC

Summary

MALNC (myeloid and AML associated intergenic long non-coding RNA, HGNC:56208) is a long non-coding RNA gene on chromosome 14q31.2.

Identifiers

Gene identifiers

Field	Value
HGNC ID	HGNC:56208
Approved symbol	MALNC
Name	myeloid and AML associated intergenic long non-coding RNA
Location	14q31.2
Locus type	RNA, long non-coding
Status	Approved
Entrez	105370601

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): RS1000010585 (14:83280356 T>C), RS1000062630 (14:83296033 C>G,T), RS1000083907 (14:83280070 C>A,G,T), RS1000126132 (14:83295659 T>C), RS1000144933 (14:83290177 T>A), RS1000413123 (14:83308002 T>C), RS1000454459 (14:83290444 C>T), RS1000505041 (14:83295738 T>C), RS1000586127 (14:83301956 G>A,T), RS1000614376 (14:83290280 T>C), RS1000671949 (14:83301397 A>G), RS1000798206 (14:83280432 T>A), RS1000802172 (14:83308296 C>T), RS1000857768 (14:83286336 T>A), RS1000989956 (14:83286068 C>T)

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.