The DONSON gene homepage

General information
Gene symbol DONSON
Gene name downstream neighbor of SON
Chromosome 21
Chromosomal band q22.1
Imprinted Unknown
Genomic reference NC_000021.8
Transcript reference NM_017613.3
Exon/intron information NM_017613.3 exon/intron table
Associated with diseases MIMIS, MISSLA
Citation reference(s) -
Refseq URL Genomic reference sequence
Curators (1) Global Variome, with Curator vacancy
Total number of public variants reported 94
Unique public DNA variants reported 39
Individuals with public variants 35
Hidden variants 5
Download all this gene's data Download all data
Notes Establishment of this gene variant database (LSDB) was supported by the Leiden University Medical Center (LUMC), Leiden, Nederland.
Date created May 03, 2013
Date last updated February 26, 2024
Version DONSON:240226

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_017613.3.
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 https://www.LOVD.nl/DONSON
HGNC 2993
Entrez Gene 29980
PubMed articles DONSON
OMIM - Gene 611428
OMIM - Diseases MIMIS (microcephaly-micromelia syndrome (MIMIS))
MISSLA (microcephaly, short stature, limb abnormalities (MISSLA))
HGMD DONSON
GeneCards DONSON
GeneTests DONSON
Orphanet DONSON


Active transcripts


ID     

Chr     

Name     

NCBI ID     

NCBI Protein ID     

DescendingVariants     
00006635 21 downstream neighbor of SON NM_017613.3 NP_060083.1 94


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