Homo sapiens aprataxin (APTX), transcript variant 18, mRNA

Run BLAST
Find regions of similarity between this sequence and other sequences using BLAST.
Pick Primers
Design and test primers for this sequence using Primer-BLAST.
Show in Genome Data Viewer
Opens the Genome Data Viewer, NCBI's genome browser, at the genomic location at which this sequence is annotated. View this sequence in the context of other features annotated at the same location and browse to other genome regions.

APTX acts in DNA double-strand break repair in a manner distinct from XRCC4. [J Radiat Res. 2023]
APTX acts in DNA double-strand break repair in a manner distinct from XRCC4.
Imamura R, Saito M, Shimada M, Kobayashi J, Ishiai M, Matsumoto Y. J Radiat Res. 2023 May 25; 64(3):485-495.
HDLBP Promotes Hepatocellular Carcinoma Proliferation and Sorafenib Resistance by Suppressing Trim71-dependent RAF1 Degradation. [Cell Mol Gastroenterol Hepatol...]
HDLBP Promotes Hepatocellular Carcinoma Proliferation and Sorafenib Resistance by Suppressing Trim71-dependent RAF1 Degradation.
Yuan J, Lv T, Yang J, Wu Z, Yan L, Yang J, Shi Y, Jiang L. Cell Mol Gastroenterol Hepatol. 2023; 15(2):307-325. Epub 2022 Oct 14.
TRABID targets DDB2 for deubiquitination to promote proliferation of hepatocellular carcinoma cells. [Biochem Biophys Res Commun. 2022]
TRABID targets DDB2 for deubiquitination to promote proliferation of hepatocellular carcinoma cells.
Chen Y, Zhang X. Biochem Biophys Res Commun. 2022 Oct 15; 625:23-30. Epub 2022 Aug 2.

RefSeq alternative splicing
See 23 reference mRNA sequence splice variants for the APTX gene.
RefSeq protein product
See the reference protein sequence for aprataxin isoform a (NP_001355926.1).

Protein
Protein sequence from Nucleotide coding region
PubMed
PubMed articles cited by Nucleotide sequence record
Taxonomy
Taxonomy sequences associated with Nucleotide record
Annotated Genomic
Genomic sequence records that have the current RNA records as annotated features marking the exons of genes.
BioSystems
BioSystems
CCDS
Link to Consensus CDS
Components (Core)
Links to Core components
Full text in PMC
Free full text articles in PMC
Gene
Link to related Genes
OMIM
OMIM records associated with Nucleotide sequence
PubMed (RefSeq)
Link to RefSeq PubMed articles
PubMed (Weighted)
Links to pubmed

Ophelia peresi[orgn] (0)
Genome
D035583 (1)
MeSH
Rare Diseases
Rare Diseases
A large group of diseases which are characterized by a low prevalence in the population. They frequently are associated with problems in diagnosis and treatment....<br/>Year introduced: 2003

MeSH
Corneal Edema
Corneal Edema
An excessive amount of fluid in the cornea due to damage of the epithelium or endothelium causing decreased visual acuity.<br/>Year introduced: 1990

MeSH
D015715 (1)
MeSH

Your browsing activity is empty.

Activity recording is turned off.

Nucleotide