The SYNE4 gene homepage

General information
Gene symbol SYNE4
Gene name spectrin repeat containing, nuclear envelope family member 4
Chromosome 19
Chromosomal band q13.12
Imprinted Unknown
Genomic reference NC_000019.9
Transcript reference NM_001039876.1
Exon/intron information NM_001039876.1 exon/intron table
Associated with diseases DFNB76
Citation reference(s) -
Refseq URL Genomic reference sequence
Curators (1) Global Variome, with Curator vacancy
Total number of public variants reported 14
Unique public DNA variants reported 11
Individuals with public variants 14
Hidden variants -
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 09, 2022
Version SYNE4:220509

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_001039876.1.
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/SYNE4
HGNC 26703
Entrez Gene 163183
PubMed articles SYNE4
OMIM - Gene 615535
OMIM - Diseases DFNB76 (deafness, autosomal recessive, type 76 (DFNB-76))
HGMD SYNE4
GeneCards SYNE4
GeneTests SYNE4
Orphanet SYNE4


Active transcripts


ID     

Chr     

Name     

NCBI ID     

NCBI Protein ID     

DescendingVariants     
00020633 19 spectrin repeat containing, nuclear envelope family member 4 NM_001039876.1 NP_001034965.1 14


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