Symbol Name ID |
Pax3
paired box 3 MGI:97487 |
* | Aspects of the system are reported to show a normal phenotype. |
Darker colors indicate more annotations |
Human Phenotypes | Abnormality of the eye |
Heterochromia iridis |
Blue irides |
Hypoplastic iris stroma |
Hypopigmentation of the fundus |
Hypertelorism |
Strabismus |
Abnormality of vision |
Lacrimation abnormality |
Ptosis |
Disease(s) Associated with PAX3 | ||||||||||
craniofacial-deafness-hand syndrome | ||||||||||
Waardenburg syndrome | ||||||||||
Waardenburg syndrome type 1 | ||||||||||
Waardenburg syndrome type 3 |
Mouse Phenotypes | vision/eye phenotype |
abnormal eyelid development |
failure of eyelid fusion |
abnormal eyelid morphology |
absent eyelids |
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Availability | Mouse Genotype | |||||
Pax3Sp-10J/Pax3+ | * | |||||
Gt(ROSA)26Sortm2(Pax3)Joe/Gt(ROSA)26Sortm2(Pax3)Joe Pax3tm1(cre)Joe/Pax3+ (conditional) |
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Gt(ROSA)26Sortm2(Pax3)Joe/Gt(ROSA)26Sortm2(Pax3)Joe H2az2Tg(Wnt1-cre)11Rth/H2az2+ (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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