TMEM131L-AS1

Summary

TMEM131L-AS1 (TMEM131L antisense RNA 1, HGNC:58899) is a long non-coding RNA gene on chromosome 4q31.3.

Identifiers

Gene identifiers

Field	Value
HGNC ID	HGNC:58899
Approved symbol	TMEM131L-AS1
Name	TMEM131L antisense RNA 1
Location	4q31.3
Locus type	RNA, long non-coding
Status	Approved
Entrez	105377498

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): RS10001304 (4:153539656 A>G), RS1000150344 (4:153534317 C>G,T), RS1000496122 (4:153537856 C>T), RS1000519054 (4:153538773 C>T), RS1000755633 (4:153533109 C>T), RS1001042052 (4:153534668 C>T), RS1001223642 (4:153527882 C>T), RS1001414198 (4:153534494 C>T), RS1001461053 (4:153533326 C>G,T), RS1001492220 (4:153533660 C>A,T), RS1001796307 (4:153534685 G>A), RS1001827372 (4:153535010 C>T), RS1001981285 (4:153538331 G>A,T), RS1002109139 (4:153537920 A>G), RS1002482253 (4:153540568 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.