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Symbol
Name
ID

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

Phenotype annotations related to embryo

Darker colors indicate more annotations

Human Phenotypes	Decreased fetal movement
Disease(s) Associated with SOX10	Decreased fetal movement
PCWH syndrome

Mouse Phenotypes

increased vagal neural crest cell apoptosis

abnormal neural crest cell migration

abnormal enteric neural crest cell migration

abnormal melanoblast migration

abnormal vagal neural crest cell migration

abnormal neural crest cell physiology

abnormal frontonasal mesenchyme morphology

abnormal neural crest morphology

abnormal enteric neural crest cell morphology

absent enteric neural crest cell

abnormal melanoblast morphology

Availability

Mouse Genotype

Sox10^Dom/Sox10^Dom

Sox10^tm1Weg/Sox10^tm1Weg

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

Sox10^tm4Weg/Sox10^tm4Weg

Sox10^Dom/Sox10⁺

Sox10^Dom/Sox10⁺
Tg(DBHn-lacZ)8Rpk/0

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)
Citing These Resources Funding Information Warranty Disclaimer, Privacy Notice, Licensing, & Copyright Send questions and comments to User Support.	last database update 04/23/2024 MGI 6.23