TMEM150C-AS1

Summary

TMEM150C-AS1 (TMEM150C antisense RNA 1, HGNC:58837) is a long non-coding RNA gene on chromosome 4q21.22.

Identifiers

Gene identifiers

Field	Value
HGNC ID	HGNC:58837
Approved symbol	TMEM150C-AS1
Name	TMEM150C antisense RNA 1
Location	4q21.22
Locus type	RNA, long non-coding
Status	Approved
Entrez	105377310

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): RS10003479 (4:82477624 C>A,G,T), RS1000913890 (4:82473246 C>A,T), RS1000998561 (4:82468678 G>A), RS1001363870 (4:82479759 C>G), RS10014975 (4:82477422 A>G), RS1001536073 (4:82478236 A>T), RS10016567 (4:82481915 C>A,G,T), RS1001729643 (4:82479576 G>A), RS1001864192 (4:82472714 T>C), RS1001974176 (4:82482601 A>G), RS1001986718 (4:82473925 A>C), RS1002428524 (4:82482325 A>G), RS1003340921 (4:82469588 C>T), RS1003604389 (4:82470717 T>C), RS1003670177 (4:82480987 T>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.