The APTX gene homepage

General information
Gene symbol APTX
Gene name aprataxin
Chromosome 9
Chromosomal band p13.3
Imprinted Unknown
Genomic reference NG_012821.1
Transcript reference NM_001195248.1, NM_001195249.1, NM_001195250.1, NM_001195251.1, NM_001195252.1, NM_001195254.1, NM_175069.2, NM_175073.2
Associated with diseases ID, Adult onset ataxia with oculomotor apraxia
Citation reference(s) -
Curators (1) Johan T. den Dunnen
Total number of public variants reported 44
Unique public DNA variants reported 7
Individuals with public variants 33
Hidden variants 137
Date created October 28, 2013
Date last updated September 28, 2016
Version APTX:160928

Graphical displays and utilities
Graphs Graphs displaying summary information of all variants in the database »
UCSC Genome Browser Show variants in the UCSC Genome Browser (full view, compact view)
Ensembl Genome Browser Show variants in the Ensembl Genome Browser (full view, compact view)
NCBI Sequence Viewer Show distribution histogram of variants in the NCBI Sequence Viewer

Links to other resources
External URL List of LSDBs for this gene
The reference LOVD for this gene, if available
HGNC HGNC:15984
Entrez Gene 54840
PubMed articles APTX
OMIM - Gene 606350
OMIM - Diseases Adult onset ataxia with oculomotor apraxia
HGMD APTX
GeneCards APTX
GeneTests APTX


Active transcripts


ID     

Chr     

Name     

NCBI ID     

NCBI Protein ID     

DescendingVariants     
00000492 9 transcript variant 10 NM_001195254.1 NP_001182183.1 44
00015699 9 Manually created transcript. NM_001195249.1 - 44
00015700 9 Manually created transcript. NM_001195251.1 - 44
00015702 9 Manually created transcript. NM_175073.2 - 44
00000490 9 transcript variant 8 NM_001195250.1 NP_001182179.1 14
00009357 9 transcript variant 6 NM_001195248.1 NP_001182177.1 14
00015701 9 Manually created transcript. (removed from reference sequence) NM_175069.2 - 14
00000491 9 transcript variant 11 NM_001195252.1 NP_001182181.1 9


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