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XB-GENEPAGE-6048313
slc9a6 solute carrier family 9, subfamily A (NHE6, cation proton antiporter 6), member 6
Monarch Ortholog Phenotypes
These phenotypes are associated with this gene with a has phenotype relation via Monarch.
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Human (60 sources): Abnormal foot morphology, Abnormal thorax morphology, Abnormality of the nose, Absent speech, Adducted thumb, Aplasia/Hypoplasia of the cerebellum, Aplasia/Hypoplasia of the corpus callosum, Arthrogryposis multiplex congenita, Autism, Bowel incontinence, [+] |
Mouse (21 sources): Purkinje cell degeneration, abnormal Purkinje cell morphology, abnormal amygdala morphology, abnormal brain cholesterol level, abnormal cerebellar molecular layer, abnormal cerebral cortex morphology, abnormal cerebral hemisphere morphology, abnormal ganglioside level, abnormal hippocampus CA3 region morphology, abnormal hippocampus CA4 region morphology, [+] |
View all ortholog results at Monarch |