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XB-GENEPAGE-481897
amn amnion associated transmembrane protein
Monarch Ortholog Phenotypes
These phenotypes are associated with this gene with a has phenotype relation via Monarch.
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Human (8 sources): Confusion, Decreased circulating vitamin B12 concentration, Dementia, Malabsorption of Vitamin B12, Megaloblastic anemia, Paresthesia, Proteinuria, Somatic sensory dysfunction |
Mouse (21 sources): abnormal ectoderm development, abnormal embryonic tissue morphology, abnormal left subclavian artery morphology, abnormal mesoderm development, abnormal nervous system development, abnormal primitive streak formation, abnormal primitive streak morphology, abnormal sternum morphology, absent amnion, absent mesoderm, [+] |
View all ortholog results at Monarch |