The SOX10 gene homepage

General information
Gene symbol SOX10
Gene name SRY (sex determining region Y)-box 10
Chromosome 22
Chromosomal band q13.1
Imprinted Unknown
Genomic reference LRG_271
Transcript reference NM_006941.3, NR_039759.1, XM_005261720.1
Associated with diseases ID, PCWH, WS-2E, WS-4C
Citation reference(s) -
Curators (1) Johan T. den Dunnen
Total number of public variants reported 45
Unique public DNA variants reported 5
Individuals with public variants 34
Hidden variants 2
Date created December 09, 2013
Date last updated September 28, 2016
Version SOX10:160928

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
External URL List of LSDBs for this gene
The reference LOVD for this gene, if available
HGNC HGNC:11190
Entrez Gene 6663
PubMed articles SOX10
OMIM - Gene 602229
OMIM - Diseases PCWH (PCWH syndrome (PCWH))
WS-2E (Waardenburg syndrome, type 2E, with or without neurologic involvement (WS-2E))
WS-4C (Waardenburg syndrome, type 4C (WS-4C))
HGMD SOX10
GeneCards SOX10
GeneTests SOX10


Active transcripts


ID     

Chr     

Name     

NCBI ID     

NCBI Protein ID     

DescendingVariants     
00027928 22 Manually created transcript NM_006941.3 - 45
00031790 22 Manually created transcript (removed from reference sequence) NR_039759.1 - -
00042580 22 transcript variant X1 XM_005261720.1 XP_005261777.1 -


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