INKILN

Summary

INKILN (inflammatory MKL1 (MRTFA) interacting lncRNA, HGNC:56260) is a long non-coding RNA gene on chromosome 4q13.3.

Identifiers

Gene identifiers

Field	Value
HGNC ID	HGNC:56260
Approved symbol	INKILN
Name	inflammatory MKL1 (MRTFA) interacting lncRNA
Location	4q13.3
Locus type	RNA, long non-coding
Status	Approved
Entrez	124900714
RNAcentral	URS00026A2198 — lncRNA, 341 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: 1 (showing top): chr4q13

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): RS1000111612 (4:73708023 A>T), RS1000143026 (4:73707734 C>T), RS1000306283 (4:73718999 G>A,C), RS1000310728 (4:73718961 A>G), RS1000394145 (4:73713033 T>C), RS1000994479 (4:73714128 C>T), RS1001144745 (4:73708887 C>T), RS1001184461 (4:73708308 T>C), RS1001234247 (4:73708324 A>C,G), RS1001321839 (4:73714337 A>G), RS1001758301 (4:73712397 G>C,T), RS1001972097 (4:73706342 G>A), RS1002142360 (4:73713891 A>T), RS1002164464 (4:73709706 G>A,T), RS1002209286 (4:73712645 T>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.