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Symbol Name ID |
Sox11
SRY (sex determining region Y)-box 11 MGI:98359 |
| * | Aspects of the system are reported to show a normal phenotype. |
| Darker colors indicate more annotations |
| Human Phenotypes | Ptosis |
| Disease(s) Associated with SOX11 | |
| Coffin-Siris syndrome 9 |
| Mouse Phenotypes | vision/eye phenotype |
increased retina apoptosis |
decreased amacrine cell number |
decreased retina ganglion cell number |
abnormal retina bipolar cell morphology |
optic nerve hypoplasia |
abnormal eye development |
microphthalmia |
abnormal eyelid morphology |
eyelids open at birth |
abnormal retina morphology |
thin retina ganglion layer |
thin retina inner nuclear layer |
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| Availability | Mouse Genotype | |||||||||||||
| Sox11tm1Weg/Sox11tm1Weg | ||||||||||||||
| Sox11tm2.2Weg/Sox11tm2.2Weg | ||||||||||||||
| Sox11tm1.1Gan/Sox11tm1.1Gan Tg(Six3-cre)69Frty/0 (conditional) |
* | |||||||||||||
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 04/16/2024 MGI 6.23 |
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