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ROGDI encodes a protein of unknown function. Additionally we are shipping Rogdi Homolog (Drosophila) Antibodies (7) and many more products for this protein.
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We identify novel compound heterozygous ROGDI mutations in five typical Kohlschutter-Tonz syndrome families. Other families were negative for ROGDI mutations, suggesting genetic heterogeneity of atypical forms of the disease.
The finding that ROGDI mutations cause Kohlschutter-Tonz Syndrome indicates that the protein product of this gene plays an important role in neuronal development as well as amelogenesis.
This gene encodes a protein of unknown function. Loss-of-function mutation in this gene cause Kohlschutter-Tonz syndrome. Alternate splicing results in multiple transcript variants.
leucine zipper domain protein
, protein rogdi homolog
, leucine-zipper-containing LZF