Symbol Name ID |
Shh
sonic hedgehog MGI:98297 |
Darker colors indicate more annotations |
Human Phenotypes | Iris coloboma |
Chorioretinal coloboma |
Optic atrophy |
Retinopathy |
Cyclopia |
Deeply set eye |
Hypertelorism |
Hypotelorism |
Proptosis |
Anophthalmia |
Microphthalmia |
Coloboma |
Ptosis |
Disease(s) Associated with SHH | |||||||||||||
holoprosencephaly | |||||||||||||
holoprosencephaly 3 | |||||||||||||
polydactyly | |||||||||||||
solitary median maxillary central incisor |
Mouse Phenotypes | abnormal retina ganglion cell morphology |
abnormal optic nerve morphology |
abnormal eye morphology |
abnormal eye development |
abnormal optic cup morphology |
abnormal optic stalk morphology |
abnormal optic vesicle formation |
cyclopia |
ocular hypertelorism |
microphthalmia |
abnormal eyelid morphology |
eyelids open at birth |
abnormal retina morphology |
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Availability | Mouse Genotype | |||||||||||||
Shhtm1.1Rseg/Shhtm1.1Rseg | ||||||||||||||
Shhtm1Chg/Shhtm1Chg | ||||||||||||||
Shhtm3(cre)Chg/Shhtm3(cre)Chg | ||||||||||||||
Shhtm1Amc/Shhtm1.1Rseg | ||||||||||||||
Tg(KRT14-Shh)#Cobm/0 | ||||||||||||||
Shhtm1(EGFP/cre)Cjt/Shhtm2Amc (conditional) | ||||||||||||||
Shhtm1Amc/Shhtm2Amc Tg(KRT14-cre)1Amc/0 (conditional) |
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Shhtm1Amc/Shhtm2Amc Tg(Thy1-cre)703Vaw/? (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 06/12/2024 MGI 6.13 |
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