HLA-DQA1-AS1

Summary

HLA-DQA1-AS1 (HLA-DQA1 antisense RNA 1, HGNC:56667) is a long non-coding RNA gene on chromosome 6p21.32.

Identifiers

Gene identifiers

Field	Value
HGNC ID	HGNC:56667
Approved symbol	HLA-DQA1-AS1
Name	HLA-DQA1 antisense RNA 1
Location	6p21.32
Locus type	RNA, long non-coding
Status	Approved
Aliases	TINA
Entrez	124901301

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): RS1002088498 (6:32640694 T>C), RS1002761579 (6:32636776 T>C), RS1004899156 (6:32641785 G>A), RS1005053647 (6:32642350 C>T), RS1005268676 (6:32638098 T>C), RS1005860817 (6:32638111 C>T), RS1006050024 (6:32635162 A>G), RS1006988011 (6:32639535 T>C), RS1007129827 (6:32635114 A>G), RS1007466641 (6:32634527 A>G), RS1008164770 (6:32640294 C>G,T), RS1008547390 (6:32634597 G>C,T), RS1008811874 (6:32641625 T>A,C), RS1009010632 (6:32636850 C>G,T), RS10093 (6:32641396 C>A,G)

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.