TODL

Summary

TODL (transcript overexpressed in dedifferentiated liposarcoma, HGNC:56636) is a long non-coding RNA gene on chromosome 12q15.

Identifiers

Gene identifiers

Field	Value
HGNC ID	HGNC:56636
Approved symbol	TODL
Name	transcript overexpressed in dedifferentiated liposarcoma
Location	12q15
Locus type	RNA, long non-coding
Status	Approved
Entrez	107984471

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): RS1000171711 (12:69010512 C>G,T), RS1000202912 (12:69006280 C>T), RS1000380270 (12:69006708 A>G), RS1000486850 (12:69012616 C>T), RS1000534983 (12:69022753 G>A), RS1000647025 (12:69017569 T>C), RS1001468336 (12:69020891 T>A), RS1001653630 (12:69005670 T>C), RS1001861600 (12:69011225 T>C), RS1001919116 (12:69016684 A>C), RS1001931092 (12:69023941 G>A,C), RS1002087109 (12:69023753 T>TTTTG), RS1002174985 (12:69012993 T>C), RS1002323373 (12:69016393 G>A), RS1002402518 (12:69022394 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.