CDH12-AS1

Summary

CDH12-AS1 (CDH12 antisense RNA 1, HGNC:59011) is a long non-coding RNA gene on chromosome 5p14.3.

Identifiers

Gene identifiers

Field	Value
HGNC ID	HGNC:59011
Approved symbol	CDH12-AS1
Name	CDH12 antisense RNA 1
Location	5p14.3
Locus type	RNA, long non-coding
Status	Approved
Entrez	105374683

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): RS1001002491 (5:21823709 C>T), RS1001408114 (5:21822687 T>A), RS1001477782 (5:21824028 G>T), RS1001736165 (5:21822394 A>G), RS1002027544 (5:21822591 A>T), RS1002317289 (5:21823763 GAAAA>G,GAAA,GAAAAA), RS1003239129 (5:21825964 A>G), RS10036078 (5:21825174 A>C,G,T), RS10036179 (5:21825552 A>C,G), RS1003757858 (5:21826845 G>T), RS1003810620 (5:21827070 C>G,T), RS10044329 (5:21825216 C>A,G,T), RS1004758001 (5:21825341 G>A), RS1004825485 (5:21824182 C>A), RS1005156342 (5:21824869 A>G)

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.