Symbol Name ID |
Nipbl
NIPBL cohesin loading factor MGI:1913976 |
Darker colors indicate more annotations |
Human Phenotypes | Increased nuchal translucency |
Proteinuria |
Disease(s) Associated with NIPBL | ||
Cornelia de Lange syndrome | ||
Cornelia de Lange syndrome 1 |
Mouse Phenotypes | abnormal DNA repair |
abnormal chemokine level |
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Availability | Mouse Genotype | ||
NipblGt(RRS564)Byg/Nipbl+ |
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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