RGPD2/3/4/6/8 Polyclonal Antibody, 20ul Enzyme Activity Assays Mutations in CBL are also

Mutations in CBL are also the cause of Noonan syndrome-like disorder

Inherited mutations in BRCA1 and this gene

pathway:Organosulfur biosynthesis

This gene was initially defined as a non-coding RNA| which is a coactivator for several nuclear receptors (NRs) and is associated with breast cancer

The contactin 6 encoded by CNTN6 is a member of the immunoglobulin superfamily

RGPD2/3/4/6/8 Polyclonal Antibody, 20ul Enzyme Activity Assays Mutations in CBL are alsoThe sequence shown here is derived from an Ensembl automatic analysis pipeline and should be considered as preliminary data.,miscellaneous: One of the 8 copies of RANBP2 clustered close to the centromere of chromosome 2.,miscellaneous: One of the 8 copies of RANBP2 clustered close to the chromosome 2 centromere.,Contains 1 GRIP domain.,Contains 2 RanBD1 domains.,Contains 2 TPR repeats.,Contains 3 TPR repeats.,tissue specificity: Expressed in testis.,