Symbol Name ID |
Sox2
SRY (sex determining region Y)-box 2 MGI:98364 |
* | Aspects of the system are reported to show a normal phenotype. |
Darker colors indicate more annotations |
Human Phenotypes | Short stature |
Growth delay |
Postnatal growth retardation |
Disease(s) Associated with SOX2 | |||
syndromic microphthalmia 3 |
Mouse Phenotypes | delayed palatal shelf elevation |
failure of palatal shelf elevation |
palatal shelves fail to meet at midline |
absent palatal taste bud |
cleft secondary palate |
abnormal tongue morphology |
abnormal fungiform papillae morphology |
embryonic growth retardation |
growth/size/body region phenotype |
decreased body size |
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Availability | Mouse Genotype | ||||||||||
Sox2tm1.1Vlcg/Sox2tm1.1Vlcg | * | ||||||||||
Sox2em1(IMPC)Mbp/Sox2+ | |||||||||||
Sox2tm1Lpev/Sox2tm3Lpev | |||||||||||
Sox2tm1Lpev/Sox2tm4Lpev | |||||||||||
Sox2tm1Rlb/Sox2+ | |||||||||||
Sox2tm2Skn/Sox2tm3Skn |
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 04/23/2024 MGI 6.23 |
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