Click here to close Hello! We notice that you are using Internet Explorer, which is not supported by Xenbase and may cause the site to display incorrectly. We suggest using a current version of Chrome, FireFox, or Safari.

Summary Expression Phenotypes Gene Literature (1) GO Terms (3) Nucleotides (41) Proteins (27) Interactants (28) Wiki
XB-GENEPAGE-853481

pcdh12     protocadherin 12

Monarch Ortholog Phenotypes
These phenotypes are associated with this gene with a has phenotype relation via Monarch.
Human (12 sources): Axial hypotonia, Dystonia, Generalized myoclonic seizure, Global developmental delay, Hyperreflexia, Intellectual disability, profound, Intrauterine growth retardation, Microcephaly, Progressive microcephaly, Secondary microcephaly, [+]
Mouse (2 sources): abnormal RR interval, no abnormal phenotype detected

View all ortholog results at Monarch