CRACD-AS1

Summary

CRACD-AS1 (CRACD antisense RNA 1, HGNC:58794) is a long non-coding RNA gene on chromosome 4q12.

Identifiers

Gene identifiers

Field	Value
HGNC ID	HGNC:58794
Approved symbol	CRACD-AS1
Name	CRACD antisense RNA 1
Location	4q12
Locus type	RNA, long non-coding
Status	Approved
Entrez	101928760

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): RS1000402781 (4:56242252 G>A), RS1000436220 (4:56245622 A>G), RS1000607689 (4:56237607 T>C), RS1000625817 (4:56243632 A>AT), RS1000680307 (4:56235826 C>T), RS1000843940 (4:56247474 T>C,G), RS1000941016 (4:56240761 G>C), RS1000982563 (4:56230170 TAAGTCCATTAC>T), RS1001076124 (4:56231520 C>T), RS1001082500 (4:56233686 A>G), RS1001149661 (4:56231698 C>T), RS1001171555 (4:56243409 A>G), RS1001514721 (4:56244268 T>C), RS1001545026 (4:56233415 T>G), RS1001614028 (4:56237620 T>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.