ROR2 Polyclonal Antibody, 20ul Petri Dishes Chromosomal translocations involving this gene

Chromosomal translocations involving this gene are well-documented and have been associated with several types of leukemia

there are multiple processed pseudogenes of RPS5 dispersed through the genome

which is a basic helix-loop-helix transcription factor known to be involved in the regulation of tissue-specific gene expression and cell differentiation

Diseases associated with C1QTNF8 include brain cancer

A nuclear localization signal (NLS) is present at the amino terminal end of the nuclear form but is lacking in the cytoplasmic form due to use of an alternate translation start codon

ROR2 Polyclonal Antibody, 20ul Petri Dishes Chromosomal translocations involving this geneThe protein encoded by ROR2 is a receptor protein tyrosine kinase and type I transmembrane protein that belongs to the ROR subfamily of cell surface receptors. The protein may be involved in the early formation of the chondrocytes and may be required for cartilage and growth plate development. Mutations in ROR2 can cause brachydactyly type B, a skeletal disorder characterized by hypoplasia aplasia of distal phalanges and nails. In addition, mutations