LINC01265

gene
On this page

Summary

LINC01265 (long intergenic non-protein coding RNA 1265, HGNC:50297) is a long non-coding RNA gene on chromosome 5p13.1.

At a glance

  • GWAS associations: 1

Identifiers

Gene identifiers

FieldValue
HGNC IDHGNC:50297
Approved symbolLINC01265
Namelong intergenic non-protein coding RNA 1265
Location5p13.1
Locus typeRNA, long non-coding
StatusApproved
Entrez101926904
RNAcentralURS000056C8F0 — lncRNA, 800 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

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):

ClassificationCount (floor)
Pathogenic0
Likely pathogenic0
Uncertain significance0
Likely benign0
Benign0

Top pathogenic / likely-pathogenic (0)

SpliceAI

0 predictions. Top by Δscore:

AlphaMissense

0 scored. Top likely-pathogenic:

dbSNP variants (sampled 300 via entrez): RS1000027164 (5:38716901 C>A), RS1000058141 (5:38717331 C>A,T), RS1000141734 (5:38710579 T>C), RS1000513371 (5:38710863 A>G,T), RS1000918158 (5:38716651 G>A,C), RS1000955921 (5:38719194 A>G), RS1001028100 (5:38718983 G>C), RS1001340997 (5:38711514 G>A,T), RS1001506277 (5:38718280 C>G), RS1001576281 (5:38717970 G>A), RS1002154701 (5:38717477 T>C), RS1002185712 (5:38717731 G>A), RS1002486734 (5:38718834 C>G), RS1002694962 (5:38711146 A>C), RS1003519167 (5:38721102 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

1 associations (top):

StudyTraitp-value
GCST003253_15Microalbuminuria8.000000e-06

Drugs & pharmacology

Drug and pharmacology data

Is drug target: no

PharmGKB: 0 entries

CTD chemical–gene interactions

2 total (human), top 2 by PubMed support.

ChemicalActions (top 5)PubMed papers
Cadmium Chloridedecreases expression1
Lactic Aciddecreases expression1

Clinical trials (associated diseases)

0 trials via MONDO — disease-level, not drug-specific.

No linked Atlas pages yet — the cross-entity mesh grows as the corpus expands.