HECTD2-AS1

gene
On this page

Summary

HECTD2-AS1 (HECTD2 antisense RNA 1, HGNC:48679) is a long non-coding RNA gene on chromosome 10q23.32.

At a glance

  • Clinical variants (ClinVar): 3 total

Identifiers

Gene identifiers

FieldValue
HGNC IDHGNC:48679
Approved symbolHECTD2-AS1
NameHECTD2 antisense RNA 1
Location10q23.32
Locus typeRNA, long non-coding
StatusApproved
Entrez100188947
RNAcentralURS000075B789 — lncRNA, 1038 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): chr10q23

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

3 variants total. Per-class counts are floors (≥ shown; pagination cap):

ClassificationCount (floor)
Pathogenic0
Likely pathogenic0
Uncertain significance2
Likely benign0
Benign0

Top pathogenic / likely-pathogenic (0)

SpliceAI

3523 predictions. Top by Δscore:

VariantEffectΔscore
10:91410574:GCG:Gdonor_gain1.0000
10:91410576:GGTA:Gdonor_loss1.0000
10:91410577:G:GGdonor_gain1.0000
10:91410578:T:Gdonor_loss1.0000
10:91425279:AG:Aacceptor_gain1.0000
10:91425280:GG:Gacceptor_gain1.0000
10:91425406:GAATG:Gdonor_gain1.0000
10:91425407:AATGG:Adonor_loss1.0000
10:91425408:ATGG:Adonor_loss1.0000
10:91425409:TGG:Tdonor_loss1.0000
10:91425410:GGTAA:Gdonor_loss1.0000
10:91425411:G:Tdonor_loss1.0000
10:91425412:T:Adonor_loss1.0000
10:91460416:A:AGacceptor_gain1.0000
10:91460417:T:Gacceptor_gain1.0000
10:91460418:A:AGacceptor_gain1.0000
10:91460419:C:Gacceptor_gain1.0000
10:91460423:A:AGacceptor_gain1.0000
10:91460423:ACAGT:Aacceptor_gain1.0000
10:91460424:CAGTG:Cacceptor_gain1.0000
10:91460425:A:AGacceptor_gain1.0000
10:91460425:AGT:Aacceptor_gain1.0000
10:91460425:AGTGA:Aacceptor_gain1.0000
10:91460426:G:GAacceptor_gain1.0000
10:91460426:GT:Gacceptor_gain1.0000
10:91460426:GTG:Gacceptor_gain1.0000
10:91460426:GTGA:Gacceptor_gain1.0000
10:91460426:GTGAG:Gacceptor_gain1.0000
10:91460561:TTTCA:Tdonor_gain1.0000
10:91460562:TTCA:Tdonor_gain1.0000

AlphaMissense

0 scored. Top likely-pathogenic:

dbSNP variants (sampled 300 via entrez): RS1000000543 (10:91556098 C>T), RS1000005287 (10:91330825 TA>T,TAA), RS1000010439 (10:91349979 A>T), RS1000015057 (10:91562855 T>C), RS1000018277 (10:91420328 G>A), RS1000019188 (10:91480561 A>G), RS1000025891 (10:91379758 G>A,C), RS1000031444 (10:91490771 G>A,C), RS1000043372 (10:91446237 G>A,T), RS1000053866 (10:91565566 T>C,G), RS1000096098 (10:91591065 C>T), RS1000132761 (10:91574890 G>A), RS1000146243 (10:91467531 G>A,T), RS1000152813 (10:91387961 G>A), RS1000214003 (10:91543940 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

CTD chemical–gene interactions

8 total (human), top 8 by PubMed support.

ChemicalActions (top 5)PubMed papers
benzo(e)pyreneincreases methylation1
fipronilaffects cotreatment, decreases expression1
Benzo(a)pyreneaffects methylation1
Cisplatinincreases expression1
DEETaffects cotreatment, decreases expression1
Methapyrileneincreases methylation1
Valproic Aciddecreases methylation1
Aflatoxin B1increases methylation1

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.