KLF11-DT

Summary

KLF11-DT (KLF11 divergent transcript, HGNC:56037) is a long non-coding RNA gene on chromosome 2p25.1.

Identifiers

Gene identifiers

Field	Value
HGNC ID	HGNC:56037
Approved symbol	KLF11-DT
Name	KLF11 divergent transcript
Location	2p25.1
Locus type	RNA, long non-coding
Status	Approved
Entrez	101929882
RNAcentral	URS0000A76AB8 — lncRNA, 563 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):

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): RS1000125111 (2:10041389 T>A), RS1000552546 (2:10044664 G>C,T), RS1000601860 (2:10041514 A>G), RS1000833672 (2:10043560 C>A,T), RS1001028882 (2:10045156 G>C), RS1002200787 (2:10042205 G>A,C), RS1002534030 (2:10044881 C>T), RS1004263220 (2:10041069 A>C,G), RS1004338237 (2:10041366 G>A,C), RS1005407250 (2:10041812 T>C,G), RS1005546095 (2:10044767 A>G), RS1005935847 (2:10041930 C>G,T), RS1006006348 (2:10042086 C>G), RS1006073700 (2:10044006 GCGGCC>G), RS1006673223 (2:10044620 G>A,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.