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TLE1 Rabbit Polyclonal Antibody, 20ul Immunology including migration
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including migration
and these and other mutations in this gene have been associated with the bone development disorder cleidocranial dysplasia (CCD)
Studies of the rat ortholog suggest that the encoded protein may instead function as a phosphatidylinositol phosphatase with the ability to dephosphorylate phosphatidylinositol 3-phosphate and phosphatidylinositol 4
RAB GTPase Binding Effector Protein 1) is a Protein Coding gene
The full-length nature of some variants has not been determined
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