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Symbol
Name
ID
Sox2
SRY (sex determining region Y)-box 2
MGI:98364
Phenotype annotations related to behavior/neurological
*Aspects of the system are reported to show a normal phenotype.
Darker colors indicate more annotations
Human Phenotypes
Psychomotor retardation
Disease(s) Associated with SOX2
microphthalmia

Mouse Phenotypes
behavior/neurological phenotype
abnormal pinna reflex
impaired righting response
abnormal placing response
impaired swimming
dystonia
head bobbing
head tossing
circling
bidirectional circling
abnormal sensory capabilities/reflexes/nociception
nonconvulsive seizures
Availability Mouse Genotype
Sox2lcc/Sox2lcc
Sox2tm1.1Vlcg/Sox2tm1.1Vlcg *
Sox2ysb/Sox2ysb
Sox2lcc/Sox2+
Sox2lcc/Sox2ysb
Sox2tm1Rlb/Sox2ysb
Sox2tm2Skn/Sox2tm3Skn

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
11/12/2019
MGI 6.14
The Jackson Laboratory