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Symbol
Name
ID
Sox2
SRY (sex determining region Y)-box 2
MGI:98364
Phenotype annotations related to growth/size/body
*Aspects of the system are reported to show a normal phenotype.
Darker colors indicate more annotations
Human Phenotypes
Congenital diaphragmatic hernia
Umbilical hernia
Short stature
Decreased body weight
Failure to thrive
Postnatal growth retardation
Disease(s) Associated with SOX2
microphthalmia

Mouse Phenotypes
abnormal palate morphology
abnormal tongue morphology
abnormal fungiform papillae morphology
growth/size/body region phenotype
decreased body size
Availability Mouse Genotype
Sox2tm1.1Vlcg/Sox2tm1.1Vlcg *
Sox2tm1Lpev/Sox2tm3Lpev
Sox2tm1Rlb/Sox2+
Sox2tm2Skn/Sox2tm3Skn
Sox2tm3(TK)Hoch/Sox2+

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