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Symbol
Name
ID

Sox10
SRY (sex determining region Y)-box 10
MGI:98358

Phenotype annotations related to growth/size/body

Darker colors indicate more annotations

Human Phenotypes	Torticollis	Splenomegaly	Hepatosplenomegaly	Hepatomegaly	Growth delay
Disease(s) Associated with SOX10
PCWH syndrome

Mouse Phenotypes		abnormal frontonasal mesenchyme morphology	decreased body weight	postnatal growth retardation
Availability	Mouse Genotype	abnormal frontonasal mesenchyme morphology	decreased body weight	postnatal growth retardation
	Sox10^tm1Weg/Sox10^tm1Weg
	Sox10^tm3(Sox8)Weg/Sox10^tm3(Sox8)Weg
	Sox10^{tm7.1(Sox10)Weg}/Sox10^{tm7.1(Sox10)Weg} Tg(Dhh-cre)1Mejr/0 (conditional)

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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