The SMCHD1 gene homepage

This database is one of the gene variant databases from the "Leiden Muscular Dystrophy pages" (LMDp).
General information
Gene symbol SMCHD1
Gene name structural maintenance of chromosomes flexible hinge domain containing 1
Chromosome 18
Chromosomal band p11.32
Imprinted Not imprinted
Genomic reference NG_031972.1
Transcript reference NM_015295.2
Exon/intron information NM_015295.2 exon/intron table
Associated with diseases BAMS, FSHD2
Citation reference(s) -
Refseq URL Coding DNA reference sequence
Curators (1) Richard Lemmers
Total number of public variants reported 615
Unique public DNA variants reported 386
Individuals with public variants 553
Hidden variants 9
Notes This database is one of the gene variant databases from the "Leiden Muscular Dystrophy pages" (LMDp).
Date created May 21, 2012
Date last updated February 26, 2024
Version SMCHD1:240226

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_015295.2.
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/SMCHD1
HGNC 29090
Entrez Gene 23347
PubMed articles SMCHD1
OMIM - Gene 614982
OMIM - Diseases BAMS (arhinia, choanal atresia, microphthalmia, Bosma type (BAMS))
FSHD2 (dystrophy, muscular, facioscapulohumeral, type 2 (FSHD-2))
HGMD SMCHD1
GeneCards SMCHD1
GeneTests SMCHD1
Orphanet SMCHD1


Active transcripts


ID     

Chr     

Name     

NCBI ID     

NCBI Protein ID     

DescendingVariants     
00000205 18 structural maintenance of chromosomes flexible hinge domain containing 1 NM_015295.2 NP_056110.2 615


Copyright & disclaimer
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