CDH18-AS2

Summary

CDH18-AS2 (CDH18 antisense RNA 2, HGNC:59009) is a long non-coding RNA gene on chromosome 5p14.3.

Identifiers

Gene identifiers

Field	Value
HGNC ID	HGNC:59009
Approved symbol	CDH18-AS2
Name	CDH18 antisense RNA 2
Location	5p14.3
Locus type	RNA, long non-coding
Status	Approved
Entrez	105374672

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): RS1000345583 (5:19773581 T>C), RS1001053575 (5:19773184 A>C), RS1001146684 (5:19772844 A>C,G), RS1001686065 (5:19769963 A>C), RS1001817584 (5:19778380 T>C), RS1001851777 (5:19777987 C>G,T), RS1002150652 (5:19771171 G>A), RS1002281279 (5:19778166 A>G), RS1002714195 (5:19775772 C>G), RS1002966967 (5:19775214 A>G), RS1003498206 (5:19777006 T>C), RS1003701000 (5:19770463 CAT>C), RS1004339920 (5:19778579 T>C), RS1004386015 (5:19774341 G>A,C), RS1004895603 (5:19773614 T>C)

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.