Symbol Name ID |
Nipbl
NIPBL cohesin loading factor MGI:1913976 |
Darker colors indicate more annotations |
Human Phenotypes | Increased nuchal translucency |
Prenatal movement abnormality |
Disease(s) Associated with NIPBL | ||
Cornelia de Lange syndrome |
Mouse Phenotypes | decreased cranial neural crest cell proliferation |
abnormal pharyngeal arch mesenchyme morphology |
decreased embryo size |
decreased embryo weight |
abnormal placenta junctional zone morphology |
abnormal spongiotrophoblast cell morphology |
abnormal placenta labyrinth morphology |
increased placenta weight |
abnormal placenta physiology |
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Availability | Mouse Genotype | |||||||||
NipblGt(EUCE313f02)1.2Hmgu/Nipbl+ | ||||||||||
NipblGt(RRS564)Byg/Nipbl+ | ||||||||||
Nipbltm1.1Hpt/Nipbltm1.1Hpt 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 05/28/2024 MGI 6.13 |
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