CDH12-AS2

Summary

CDH12-AS2 (CDH12 antisense RNA 2, HGNC:59012) is a long non-coding RNA gene on chromosome 5p14.3.

Identifiers

Gene identifiers

Field	Value
HGNC ID	HGNC:59012
Approved symbol	CDH12-AS2
Name	CDH12 antisense RNA 2
Location	5p14.3
Locus type	RNA, long non-coding
Status	Approved
Entrez	107986345

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): RS1000393472 (5:21967856 G>T), RS1000754101 (5:21966322 A>G), RS1001145192 (5:21966592 T>C), RS1003232022 (5:21968141 G>A), RS1003695653 (5:21967898 A>G), RS1004962764 (5:21966736 G>C), RS10055932 (5:21967049 A>C), RS1007283705 (5:21968979 G>A,C,T), RS1009425433 (5:21965936 C>A,T), RS1011949511 (5:21967693 C>G), RS1013191718 (5:21967875 C>T), RS1013529509 (5:21966665 C>T), RS1014713769 (5:21967910 C>T), RS1018841174 (5:21968285 T>C,G), RS1020466155 (5:21967328 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.