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Symbol
Name
ID

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

Phenotype annotations related to integument

!	Indicates phenotype varies with strain background.
	Darker colors indicate more annotations

Human Phenotypes	Abnormal eyebrow morphology	White eyebrow	White eyelashes	Hypopigmentation of hair	White forelock	Premature graying of hair	Hypohidrosis	Cafe-au-lait spot	Hypopigmented skin patches
Disease(s) Associated with SOX10	Abnormal eyebrow morphology	White eyebrow	White eyelashes	Hypopigmentation of hair	White forelock	Premature graying of hair	Hypohidrosis	Cafe-au-lait spot	Hypopigmented skin patches
PCWH syndrome
Waardenburg syndrome type 2E
Waardenburg syndrome type 4C

Mouse Phenotypes

abnormal coat/hair pigmentation

darkened coat color

absent hair follicle melanin granules

absent coat pigmentation

diluted coat color

head blaze

white spotting

belly spot

variable body spotting

decreased foot pigmentation

decreased tail pigmentation

non-pigmented tail tip

absent skin pigmentation

Availability

Mouse Genotype

Sox10^gt/Sox10^gt

!

Sox10^tm3(Sox8)Weg/Sox10^tm3(Sox8)Weg

Sox10^Dal/Sox10⁺

Sox10^df8R/Sox10⁺

Sox10^Dom/Sox10⁺

Sox10^Dom/Sox10⁺
Tg(DBHn-lacZ)8Rpk/0

Sox10^gt/Sox10^tm1Weg

Sox10^M2J/Sox10⁺

Sox10^tm1Weg/Sox10⁺

Sox10^tm2(rtTA)Weg/Sox10⁺

Sox10^tm4Weg/Sox10⁺

Sox10^tm8.1Weg/Sox10⁺

Sox10^M2Btlr/?

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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