SMG9 gene homepage

General information
Gene symbol SMG9
Gene name smg-9 homolog, nonsense mediated mRNA decay factor (C. elegans)
Chromosome 19
Chromosomal band q13.31
Imprinted Unknown
Genomic reference NC_000019.9
Transcript reference NM_019108.2
Exon/intron information NM_019108.2 exon/intron table
Associated with diseases HBMS
Citation reference(s) -
Refseq URL Genomic reference sequence
Curators (1) LOVD-team, but with Curator vacancy
Total number of public variants reported 6
Unique public DNA variants reported 5
Individuals with public variants 5
Hidden variants 0
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 May 17, 2019
Version SMG9:190517

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_019108.2.
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/SMG9
HGNC 25763
Entrez Gene 56006
PubMed articles SMG9
OMIM - Gene 613176
OMIM - Diseases HBMS (malformation, heart and brain, syndrome (HBMS))
HGMD SMG9
GeneCards SMG9
GeneTests SMG9


Active transcripts


ID     

Chr     

Name     

NCBI ID     

NCBI Protein ID     

DescendingVariants     
00019453 19 smg-9 homolog, nonsense mediated mRNA decay factor (C. elegans) NM_019108.2 NP_061981.2 6


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