PCDH9-AS4
gene geneOn this page
Summary
PCDH9-AS4 (PCDH9 antisense RNA 4, HGNC:40428) is a long non-coding RNA gene on chromosome 13q21.32.
Identifiers
Gene identifiers
| Field | Value |
|---|---|
| HGNC ID | HGNC:40428 |
| Approved symbol | PCDH9-AS4 |
| Name | PCDH9 antisense RNA 4 |
| Location | 13q21.32 |
| Locus type | RNA, long non-coding |
| Status | Approved |
| Ensembl gene | ENSG00000233840 |
| Entrez | 100874087 |
| RNAcentral | URS000075BBAD — lncRNA, 429 nt, 1 organism(s) |
Gene structure
Transcript identifiers
Ensembl transcripts: 0
RefSeq mRNA: 0 — MANE Select: None
Canonical transcript exons
None — 0 exons
Expression profiles
Bgee: expression breadth broad, 73 present calls, max score 98.87.
Top tissues by expression
73 total, by Bgee expression score (0-100, higher = more expressed):
| Tissue | Anatomy ID | Expression score | Quality |
|---|---|---|---|
| corpus callosum | UBERON:0002336 | 98.87 | gold quality |
| male germ line stem cell (sensu Vertebrata) in testis | CL:0000089 ∩ UBERON:0000473 | 83.41 | gold quality |
| sural nerve | UBERON:0015488 | 78.17 | gold quality |
| calcaneal tendon | UBERON:0003701 | 74.46 | gold quality |
| colonic epithelium | UBERON:0000397 | 73.95 | gold quality |
| bone marrow cell | CL:0002092 | 71.90 | silver quality |
| skeletal muscle tissue | UBERON:0001134 | 68.19 | silver quality |
| kidney | UBERON:0002113 | 65.09 | gold quality |
| adrenal tissue | UBERON:0018303 | 58.88 | gold quality |
| primary visual cortex | UBERON:0002436 | 56.73 | gold quality |
| monocyte | CL:0000576 | 56.47 | gold quality |
| superior frontal gyrus | UBERON:0002661 | 55.89 | gold quality |
| prefrontal cortex | UBERON:0000451 | 55.60 | gold quality |
| adrenal gland | UBERON:0002369 | 55.35 | gold quality |
| intestine | UBERON:0000160 | 54.84 | gold quality |
| testis | UBERON:0000473 | 54.63 | gold quality |
| left testis | UBERON:0004533 | 54.63 | gold quality |
| pancreas | UBERON:0001264 | 54.58 | gold quality |
| right testis | UBERON:0004534 | 53.89 | gold quality |
| gastrocnemius | UBERON:0001388 | 53.55 | gold quality |
| lung | UBERON:0002048 | 52.69 | gold quality |
| stomach | UBERON:0000945 | 52.32 | gold quality |
| heart | UBERON:0000948 | 51.42 | gold quality |
| blood | UBERON:0000178 | 49.91 | gold quality |
| esophagogastric junction muscularis propria | UBERON:0035841 | 49.68 | gold quality |
| body of pancreas | UBERON:0001150 | 49.66 | gold quality |
| multicellular organism | UBERON:0000468 | 49.54 | gold quality |
| Ammon’s horn | UBERON:0001954 | 47.35 | gold quality |
| liver | UBERON:0002107 | 47.10 | silver quality |
| Brodmann (1909) area 9 | UBERON:0013540 | 47.10 | gold quality |
Single-cell (SCXA)
Detected in 1 experiment(s), a significant marker in 0.
| Experiment | Marker? | Max mean expression |
|---|---|---|
| E-ANND-3 | no | 0.96 |
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): RS1000421942 (13:66990101 A>T), RS1000858136 (13:66992653 C>G,T), RS1000889337 (13:66992381 T>C), RS1000935805 (13:66999925 G>A,T), RS1001078999 (13:66999428 A>G), RS1001144757 (13:66996681 T>C), RS1001290654 (13:66991852 T>C,G), RS1001486454 (13:66998208 A>G), RS1001537355 (13:66998525 A>G), RS1001702899 (13:66991512 A>C,G), RS1001984400 (13:66992949 A>C,G), RS1002048989 (13:66991295 T>C), RS1002297912 (13:66993402 A>T), RS1002410915 (13:66993158 C>G,T), RS1002438022 (13:66993265 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.
Related Atlas pages
No linked Atlas pages yet — the cross-entity mesh grows as the corpus expands.