ABHD16A-AS1

Summary

ABHD16A-AS1 (ABHD16A antisense RNA 1, HGNC:59161) is a long non-coding RNA gene on chromosome 6p21.33.

Identifiers

Gene identifiers

Field	Value
HGNC ID	HGNC:59161
Approved symbol	ABHD16A-AS1
Name	ABHD16A antisense RNA 1
Location	6p21.33
Locus type	RNA, long non-coding
Status	Approved
Entrez	105375018

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): RS1000470101 (6:31688011 C>A), RS1002085157 (6:31689845 T>C,G), RS1002139009 (6:31689522 G>A,C,T), RS1003694889 (6:31688776 C>T), RS1004220585 (6:31691284 T>G), RS1004239277 (6:31691243 A>G), RS1006586195 (6:31689253 A>C,G), RS1007070061 (6:31688344 G>A), RS1008722141 (6:31690414 C>A,G), RS1010075709 (6:31690766 AGAG>A), RS1010429476 (6:31688279 C>G,T), RS1011491490 (6:31689208 C>A,T), RS1012513312 (6:31688302 G>GT), RS1013495626 (6:31689201 C>A,G,T), RS1013695797 (6:31689497 C>T)

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.