TENM3-AS3

Summary

TENM3-AS3 (TENM3 antisense RNA 3, HGNC:58915) is a long non-coding RNA gene on chromosome 4q35.1.

Identifiers

Gene identifiers

Field	Value
HGNC ID	HGNC:58915
Approved symbol	TENM3-AS3
Name	TENM3 antisense RNA 3
Location	4q35.1
Locus type	RNA, long non-coding
Status	Approved
Entrez	105377571

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): RS10002126 (4:182765602 G>A), RS1000744737 (4:182765898 A>G), RS1001716506 (4:182766090 C>G,T), RS10017238 (4:182766636 T>A,C), RS1001933322 (4:182765944 T>C), RS1002010818 (4:182761193 C>T), RS1002105567 (4:182761393 T>A,C), RS1002724060 (4:182763511 G>C), RS1002755198 (4:182763706 T>C), RS1003135122 (4:182767070 CT>C), RS1003503112 (4:182762314 C>T), RS1003634002 (4:182767593 G>T), RS1003778469 (4:182762569 T>C), RS1003867693 (4:182766169 G>T), RS1003941138 (4:182766428 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.