MP:0001701 | incomplete embryo turning | "arrest of the axial rotation of the germ layers of the embryo during the primitive streak/early somite stage (E8.5-E9.5)" [J:62571] |
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Allelic Composition: Map2k7tm2.1Rjd/Map2k7tm2.1Rjd Genetic Background: B6.129S6-Map2k7tm2.1Rjd
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MP:0001723 | disorganized vascular plexus | |
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Allelic Composition: Map2k7tm2.1Rjd/Map2k7tm2.1Rjd Genetic Background: B6.129S6-Map2k7tm2.1Rjd
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MP:0001914 | hemorrhage | "loss of blood from the vascular compartment to the exterior or into nonvascular body space as a result of rupture or severance of the blood vessels" [Stedman s Medical Dictionary, 27th edition:ISBN 0-683-40008-8] |
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Allelic Composition: Map2k7tm2.1Rjd/Map2k7tm2.1Rjd Genetic Background: B6.129S6-Map2k7tm2.1Rjd
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MP:0002621 | delayed neural tube closure | "delayed fusion of the neuroepithelial layer in early development" [J:79790, cml:Cathleen M. Lutz , Mouse Genome Informatics Curator] |
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Allelic Composition: Map2k7tm2.1Rjd/Map2k7tm2.1Rjd Genetic Background: B6.129S6-Map2k7tm2.1Rjd
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MP:0003984 | embryonic growth retardation | "slow or limited development before birth" [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator] |
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Allelic Composition: Map2k7tm2.1Rjd/Map2k7tm2.1Rjd Genetic Background: B6.129S6-Map2k7tm2.1Rjd
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MP:0005312 | pericardial effusion | "escape of fluid from blood vessels or lymphatics into the fibrous sac surrounding the heart" [Stedman s Medical Dictionary:ISBN 0-683-40008-8] |
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Allelic Composition: Map2k7tm2.1Rjd/Map2k7tm2.1Rjd Genetic Background: B6.129S6-Map2k7tm2.1Rjd
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MP:0006042 | increased apoptosis | "greater than normal programmed cell death" [RGD:Rat Genome Database submission, smb:Susan M Bello, Mouse Genome Informatics Curator] |
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Allelic Composition: Map2k7tm2.1Rjd/Map2k7tm2.1Rjd Genetic Background: B6.129S6-Map2k7tm2.1Rjd
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MP:0011098 | complete embryonic lethality during organogenesis | "death of all organisms of a given genotype in a population between embryo turning and the completion of organogenesis (Mus: E9 to less than E14)" [MGI:csmith] |
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Allelic Composition: Map2k7tm2.1Rjd/Map2k7tm2.1Rjd Genetic Background: B6.129S6-Map2k7tm2.1Rjd
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MP:0011260 | abnormal head mesenchyme morphology | "any structural anomaly of the primordial embryonic connective tissue of the developing head, consisting of mesenchymal cells supported in interlaminar jelly, that derive mostly from the mesoderm and contribute to head connective tissue, bone and musculature in conjunction with cranial neural crest cells" [ISBN:0-683-40008-8] |
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Allelic Composition: Map2k7tm2.1Rjd/Map2k7tm2.1Rjd Genetic Background: B6.129S6-Map2k7tm2.1Rjd
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