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XB-GENEPAGE-489102
smarcd2 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily d, member 2
Monarch Ortholog Phenotypes
These phenotypes are associated with this gene with a has phenotype relation via Monarch.
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Human (19 sources): Abnormal pinna morphology, Absent neutrophil specific granules, Anemia, Brachydactyly, Diarrhea, Failure to thrive, Fragile nails, Global developmental delay, Hirsutism, Low-set ears, [+] |
Mouse (6 sources): abnormal circulating alanine transaminase level, abnormal circulating aspartate transaminase level, abnormal embryo size, decreased circulating alanine transaminase level, decreased circulating aspartate transaminase level, preweaning lethality, incomplete penetrance |
View all ortholog results at Monarch |