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All Matches for Sox10
You searched for: sry. Also searched for: sri-.
Symbol
Name
ID
Sox10
SRY (sex determining region Y)-box 10
MGI:98358

Nomenclature or ID Symbol, Name, Synonym and Accession ID matches to your query for this genome feature.
  Score Nomenclature or ID
Name : SRY (sex determining region Y)-box 10
Old Name : SRY-box containing gene 21
Human Name : SRY-box transcription factor 10

Vocabulary Terms Term, Synonym, and Definition matches to your query that are associated with this genome feature.
  Score Annotated Term
Disease Ortholog : PCWH syndrome
    from its definition : A syndrome that is characterized by the association of the features of Waardenburg-Shah syndrome (sensorineural hearing loss, pigmentary abnormalities and Hirschsprung disease; see this term) with neurological features, including: neonatal hypotonia, intellectual deficit (of variable severity), nystagmus, progressive spasticity, ataxia and epilepsy, and has_material_basis_in heterozygous mutation in the SRY-box 10 (SOX10) gene on chromosome 22q13.

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB), Gene Ontology (GO)
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last database update
10/12/2021
MGI 6.17
The Jackson Laboratory