MICA-AS1

Summary

MICA-AS1 (MICA antisense RNA 1, HGNC:53631) is a long non-coding RNA gene on chromosome 6p21.33.

Identifiers

Gene identifiers

Field	Value
HGNC ID	HGNC:53631
Approved symbol	MICA-AS1
Name	MICA antisense RNA 1
Location	6p21.33
Locus type	RNA, long non-coding
Status	Approved
Entrez	101929072
RNAcentral	URS0000BC4549 — lncRNA, 1373 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: 4 (showing top): RATTENBACHER_BOUND_BY_CELF1, ZNF197_TARGET_GENES, GSE25087_FETAL_VS_ADULT_TREG_DN, chr6p21

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): RS1000359507 (6:31399954 A>G), RS1000911754 (6:31398009 C>G,T), RS1000983545 (6:31397540 ACT>A), RS1001639582 (6:31398435 G>A), RS1002089020 (6:31397378 C>T), RS1002567303 (6:31397019 T>A), RS1002631569 (6:31402112 AT>A,ATT), RS1004828011 (6:31398679 G>C,T), RS1005186514 (6:31397015 T>C), RS1005404062 (6:31396716 A>C), RS1006356045 (6:31401758 C>T), RS1008290492 (6:31394543 G>A), RS1008870939 (6:31401326 A>G), RS1011069650 (6:31396127 C>T), RS1011695217 (6:31401279 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.