Symbol Name ID |
Pkn2
protein kinase N2 MGI:109211 |
Darker colors indicate more annotations |
Mouse Phenotypes | abnormal vitelline vasculature morphology |
absent vitelline blood vessels |
disorganized yolk sac vascular plexus |
increased embryonic tissue cell apoptosis |
abnormal neural crest cell migration |
absent pharyngeal arches |
abnormal developmental patterning |
abnormal embryo turning |
abnormal rostral-caudal body axis extension |
abnormal embryo morphology |
abnormal germ layer morphology |
abnormal mesoderm morphology |
abnormal mesenchyme morphology |
abnormal neural fold formation |
abnormal neural tube morphology |
open neural tube |
craniorachischisis |
abnormal somite development |
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Availability | Mouse Genotype | ||||||||||||||||||
Pkn2tm1a(KOMP)Wtsi/Pkn2tm1a(KOMP)Wtsi | |||||||||||||||||||
Gt(ROSA)26Sortm9(cre/ESR1)Arte/Gt(ROSA)26Sor+ Pkn2tm1c(KOMP)Wtsi/Pkn2tm1c(KOMP)Wtsi (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 04/16/2024 MGI 6.23 |
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