KAT6A-AS1

Summary

KAT6A-AS1 (KAT6A antisense RNA 1, HGNC:56157) is a long non-coding RNA gene on chromosome 8p11.21.

Identifiers

Gene identifiers

Field	Value
HGNC ID	HGNC:56157
Approved symbol	KAT6A-AS1
Name	KAT6A antisense RNA 1
Location	8p11.21
Locus type	RNA, long non-coding
Status	Approved
Entrez	105379393
RNAcentral	URS0000A76588 — lncRNA, 1160 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): RS1000032426 (8:42058052 C>T), RS1000064889 (8:42074892 C>T), RS1000102876 (8:42070156 C>T), RS1000198259 (8:42103111 A>G), RS1000243023 (8:42061967 A>G,T), RS1000282930 (8:42073510 T>C), RS1000327185 (8:42067667 A>G), RS1000379697 (8:42067879 G>A,C), RS1000413038 (8:42095224 A>G), RS1000456927 (8:42051296 A>C), RS1000579108 (8:42080058 T>G), RS1000587512 (8:42063465 T>C), RS1000590086 (8:42087283 C>T), RS1000609013 (8:42104769 A>G), RS1000635422 (8:42056785 G>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.