Symbol Name ID |
Mib1
MIB E3 ubiquitin protein ligase 1 MGI:2443157 |
Darker colors indicate more annotations |
Mouse Phenotypes | abnormal vitelline vasculature morphology |
absent vitelline blood vessels |
absent second pharyngeal arch |
abnormal rostral-caudal axis patterning |
caudal body truncation |
embryonic growth retardation |
abnormal paraxial mesoderm morphology |
abnormal neural tube morphology |
abnormal embryonic neuroepithelium morphology |
abnormal embryonic neuroepithelial layer differentiation |
kinked neural tube |
abnormal notochord morphology |
abnormal dorsal-ventral polarity of the somites |
abnormal somite shape |
fused somites |
failure of somite differentiation |
incomplete somite formation |
abnormal visceral yolk sac morphology |
failure of chorioallantoic fusion |
abnormal vitelline vascular remodeling |
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Availability | Mouse Genotype | ||||||||||||||||||||
Mib1tm1Art/Mib1tm1Art | |||||||||||||||||||||
Mib1tm1Kong/Mib1tm1Kong | |||||||||||||||||||||
Mib1tm2Kong/Mib1tm2Kong Tg(Tek-cre)12Flv/0 (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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