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Symbol
Name
ID

Sox9
SRY (sex determining region Y)-box 9
MGI:98371

Phenotype annotations related to nervous system

Darker colors indicate more annotations

Human Phenotypes	Abnormality of the sense of smell	Hydrocephalus	Ventriculomegaly	Spinal dysraphism	Spina bifida	Hypoplasia of olfactory tract	Global developmental delay	Mild global developmental delay	Moderate global developmental delay	Seizure
Disease(s) Associated with SOX9
campomelic dysplasia

Mouse Phenotypes		impaired cranial neural crest cell differentiation	abnormal trunk neural crest cell morphology	abnormal dorsal root ganglion morphology
Availability	Mouse Genotype	impaired cranial neural crest cell differentiation	abnormal trunk neural crest cell morphology	abnormal dorsal root ganglion morphology
	Sox9^tm1Gsr/Sox9^tm1Gsr Krt19^tm1(cre)Mmt/Krt19⁺ (conditional)
	Sox9^tm2Crm/Sox9^tm2Crm Tg(Zp3-cre)93Knw/? (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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