CEP135-AS1

Summary

CEP135-AS1 (CEP135 antisense RNA 1, HGNC:58793) is a long non-coding RNA gene on chromosome 4q12.

Identifiers

Gene identifiers

Field	Value
HGNC ID	HGNC:58793
Approved symbol	CEP135-AS1
Name	CEP135 antisense RNA 1
Location	4q12
Locus type	RNA, long non-coding
Status	Approved
Entrez	124900705

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): RS1000092702 (4:55960787 G>A), RS1000303447 (4:55970295 A>G), RS1000494718 (4:55965431 A>G), RS1000572870 (4:55972229 C>T), RS1000578121 (4:55955785 G>A), RS1000630361 (4:55956019 T>C), RS1001007037 (4:55971972 G>A), RS1001058534 (4:55966043 T>A), RS1001264121 (4:55952805 G>A), RS1001585581 (4:55964726 G>T), RS1001669633 (4:55970351 A>G), RS1001695542 (4:55953345 C>G,T), RS1001721858 (4:55970651 T>A), RS10017805 (4:55967672 C>A), RS1001847241 (4:55966379 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.