DNA2 gene homepage

General information
Gene symbol DNA2
Gene name DNA replication helicase 2 homolog (yeast)
Chromosome 10
Chromosomal band q21.3-q22.1
Imprinted Unknown
Genomic reference NC_000010.10
Transcript reference NM_001080449.2
Exon/intron information NM_001080449.2 exon/intron table
Associated with diseases PEOA-6, SCKL-8
Citation reference(s) -
Refseq URL Genomic reference sequence
Curators (1) LOVD-team, but with Curator vacancy
Total number of public variants reported 27
Unique public DNA variants reported 24
Individuals with public variants 11
Hidden variants 0
Date created May 03, 2013
Date last updated May 03, 2019
Version DNA2:190503

Graphical displays and utilities
Graphs Graphs displaying summary information of all variants in the database »
Reading frame checker The Reading-frame checker generates a prediction of the effect of whole-exon changes. Active for: NM_001080449.2.
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
Homepage URL http://www.LOVD.nl/DNA2
HGNC 2939
Entrez Gene 1763
PubMed articles DNA2
OMIM - Gene 601810
OMIM - Diseases PEOA-6 (ophthalmoplegia, external, progressive, with mitochondrial DNA deletions, autosomal dominant, type 6 (PEOA-6))
SCKL-8 (Seckel syndrome, type 8 (SCKL-8))
HGMD DNA2
GeneCards DNA2
GeneTests DNA2


Active transcripts


ID     

Chr     

Name     

NCBI ID     

NCBI Protein ID     

DescendingVariants     
00006512 10 DNA replication helicase 2 homolog (yeast) NM_001080449.2 NP_001073918.2 27


Copyright & disclaimer
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