SOX10

Information SOX10

Description

This gene encodes a member of the SOX (SRY-related HMG-box) family of transcription factors involved in the regulation of embryonic development and in the determination of the cell fate. The encoded protein may act as a transcriptional activator after forming a protein complex with other proteins. This protein acts as a nucleocytoplasmic shuttle protein and is important for neural crest and peripheral nervous system development. Mutations in this gene are associated with Waardenburg-Shah and Waardenburg-Hirschsprung disease. [provided by RefSeq, Jul 2008]

Full Name

SRY-box transcription factor 10

Source NCBI

Species

Homo sapiens [tax_id: 9606]

Genome

hg38

ReMap Statistics

Datasets
1
Biotypes
1
Peaks
4,198
Non-redundant peaks
4,198

TF Classification

Super Class
Other all-alpha-helical DNA-binding domains
Class
High-mobility group (HMG) domain factors
Familly
SOX-related factors
Sub Familly
Group E

Source TFClass

External IDs

NCBI Gene
6663
Official Gene Name
SOX10
JASPAR
MA0442
Ensembl
ENSG00000100146
UniProt
P56693
Genevisible
P56693
RefSeq
NM_006941
Aliases
DOM; PCWH; WS2E; WS4; WS4C
All peaks SOX10
Download BED file
Non redundant peaks SOX10
Download BED file
SEQUENCES SOX10
Download FASTA file
DOWNLOAD All ReMap
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Datasets Table for SOX10

Target name Target modification Ecotype/Strain Biotype Biotype modification Source Species Experiment Peaks
SOX10 501-mel GEO Homo sapiens GSE61965 4,198
Target name Target modification Ecotype/Strain Biotype Biotype modification Source Species Experiment Peaks