Symbol Name ID |
Nup133
nucleoporin 133 MGI:2442620 |
Darker colors indicate more annotations |
Human Phenotypes | Microcephaly |
Aqueductal stenosis |
Pachygyria |
Abnormality of neuronal migration |
Hemiplegia/hemiparesis |
EEG abnormality |
Cognitive impairment |
Global developmental delay |
Seizure |
Disease(s) Associated with NUP133 | |||||||||
Galloway-Mowat syndrome |
Mouse Phenotypes | abnormal neural tube morphology |
kinked neural tube |
abnormal nervous system morphology |
abnormal nervous system development |
exencephaly |
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Availability | Mouse Genotype | |||||
Nup133Gt(RRK090)Byg/Nup133Gt(RRK090)Byg | ||||||
Nup133mermaid/Nup133mermaid |
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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