Symbol Name ID |
Prrx1
paired related homeobox 1 MGI:97712 |
Darker colors indicate more annotations |
Human Phenotypes | Abnormal cranial nerve morphology |
Agenesis of corpus callosum |
Aplasia/Hypoplasia of the cerebellum |
Holoprosencephaly |
Disease(s) Associated with PRRX1 | ||||
agnathia-otocephaly complex |
Mouse Phenotypes | spina bifida |
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Availability | Mouse Genotype | |
Prrx1tm1Tex/Prrx1tm1Tex |
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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