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XB-GENEPAGE-999368
		cnnm2 cyclin and CBS domain divalent metal cation transport mediator 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 myelination, Absent speech, Autistic behavior, Generalized muscle weakness, Global developmental delay, Headache, Hyperactive deep tendon reflexes, Hypermagnesiuria, Hypomagnesemia, Intellectual disability, [+] | 
| Mouse (6 sources): abnormal craniofacial morphology, abnormal head size, abnormal startle reflex, decreased startle reflex, preweaning lethality, complete penetrance, shortened RR interval | 
| View all ortholog results at Monarch | 
