tln1 Phenotypes

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Monarch Ortholog Phenotypes These phenotypes are associated with this gene with a has phenotype relation via Monarch.
Mouse (31 sources): abnormal amniotic cavity morphology, abnormal ectoderm development, abnormal embryo development, abnormal embryonic tissue morphology, abnormal extraembryonic mesoderm development, abnormal extraembryonic tissue morphology, abnormal gastrulation movements, abnormal megakaryocyte morphology, abnormal mesoderm development, abnormal platelet activation, abnormal proamniotic cavity morphology, abnormal thrombosis, abnormal trophoblast layer morphology, absent ectoplacental cavity, absent extraembryonic coelom, decreased embryo size, decreased hematocrit, decreased hemoglobin content, disorganized extraembryonic tissue, embryonic growth arrest, embryonic lethality between somite formation and embryo turning, complete penetrance, embryonic lethality during organogenesis, complete penetrance, embryonic lethality, complete penetrance, embryonic-extraembryonic boundary constriction, immune system phenotype, low mean erythrocyte cell number, postnatal lethality, incomplete penetrance, premature death, reduced thrombolysis, small amniotic cavity, small proamniotic cavity [+]

Monarch Ortholog Phenotypes

These phenotypes are associated with this gene with a has phenotype relation via Monarch.

Mouse (31 sources): abnormal amniotic cavity morphology, abnormal ectoderm development, abnormal embryo development, abnormal embryonic tissue morphology, abnormal extraembryonic mesoderm development, abnormal extraembryonic tissue morphology, abnormal gastrulation movements, abnormal megakaryocyte morphology, abnormal mesoderm development, abnormal platelet activation, [+]