View gene SMARCE1

General information
Gene symbol SMARCE1
Gene name SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily e, member 1
Chromosome 17
Chromosomal band q21.2
Imprinted Unknown
Genomic reference NG_032163.1
Transcript reference NM_003079.4
Exon/intron information NM_003079.4
Associated with diseases meningioma
Citation reference(s) -
Refseq URL Genomic reference sequence
Curators (1) LOVD-team, but with Curator vacancy
Total number of public variants reported 3
Unique public DNA variants reported 3
Individuals with public variants 3
Hidden variants 0
Notes Establishment of this gene variant database (LSDB) was supported by the European Community's Seventh Framework Programme (FP7/2007-2013) under grant agreement No 200754 - the GEN2PHEN project.
Date created March 20, 2012
Date last updated January 10, 2016
Version SMARCE1:160110

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
Homepage URL http://www.LOVD.nl/SMARCE1
External URL Orphanet
HGNC 11109
Entrez Gene 6605
PubMed articles SMARCE1
OMIM - Gene 603111
OMIM - Diseases meningioma (meningioma, familial, susceptibility to)
HGMD SMARCE1
GeneCards SMARCE1
GeneTests SMARCE1


Active transcripts


ID     

Chr     

Name     

NCBI ID     

NCBI Protein ID     

DescendingVariants     
00019429 17 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily e, member 1 NM_003079.4 NP_003070.3 3


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