HP1 alpha(Phospho Ser92) Polyclonal Antibody, 100ul Cryopreservation Mutations in KAL1 cause the

Mutations in KAL1 cause the X-linked Kallmann syndrome

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it is now thought that the RBM8B locus is a pseudogene

This gene is also involved in several chromosomal translocations that are associated with lymphoid malignancies including pre-B-cell acute lymphoblastic leukemia (t(1|19)

|subcellular location:When uncleaved| it is predominantly cytoplasmic

HP1 alpha(Phospho Ser92) Polyclonal Antibody, 100ul Cryopreservation Mutations in KAL1 cause theThis gene encodes a highly conserved nonhistone protein, which is a member of the heterochromatin protein family. The protein is enriched in the heterochromatin and associated with centromeres. The protein has a single N terminal chromodomain which can bind to histone proteins via methylated lysine residues, and a C terminal chromo shadow domain (CSD) which is responsible for the homodimerization and interaction with a number of chromatin associated