CDH12-AS4

Summary

CDH12-AS4 (CDH12 antisense RNA 4, HGNC:59014) is a long non-coding RNA gene on chromosome 5p14.3.

Identifiers

Gene identifiers

Field	Value
HGNC ID	HGNC:59014
Approved symbol	CDH12-AS4
Name	CDH12 antisense RNA 4
Location	5p14.3
Locus type	RNA, long non-coding
Status	Approved
Entrez	105374681

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): RS1000218469 (5:22581271 C>A,T), RS1000375312 (5:22586699 T>A), RS1000414933 (5:22571878 C>T), RS1000427519 (5:22586404 G>A,T), RS1000716002 (5:22580923 T>C), RS1000722214 (5:22575556 C>A,T), RS1000776233 (5:22575341 G>A), RS1001113467 (5:22581727 A>G), RS1001264274 (5:22574839 G>A,C), RS1001281669 (5:22586207 G>A), RS1001322686 (5:22579796 T>C), RS1001334065 (5:22586429 T>C), RS1001427881 (5:22585391 T>C,G), RS1001491804 (5:22580610 G>T), RS1001780155 (5:22573946 G>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.