Symbol Name ID |
Ofd1
OFD1, centriole and centriolar satellite protein MGI:1350328 |
* | Aspects of the system are reported to show a normal phenotype. |
Darker colors indicate more annotations |
Human Phenotypes | Polyhydramnios |
Disease(s) Associated with OFD1 | |
Joubert syndrome 10 |
Mouse Phenotypes | embryo phenotype |
incomplete embryo turning |
abnormal left-right axis patterning |
decreased embryo size |
abnormal limb mesenchyme morphology |
absent floor plate |
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Availability | Mouse Genotype | ||||||
Ofd1tm1Bfra/Ofd1tm1Bfra | |||||||
Ofd1tm2.1Bfra/Ofd1+ Tg(CAG-cre)1Nagy/0 (conditional) |
* | ||||||
Ofd1tm2.1Bfra/Ofd1+ Tg(Prrx1-cre)1Cjt/0 (conditional) |
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Ofd1tm2.1Bfra/Y Tg(CAG-cre)1Nagy/0 (conditional) |
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Ofd1tm2.1Bfra/Y Tg(Prrx1-cre)1Cjt/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 08/21/2024 MGI 6.24 |
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