DMRTB Polyclonal Antibody, 100ul Nucleic Acid Isolation & Purification Mutations associated with this gene

Mutations associated with this gene cause the most frequent form of autosomal dominant spastic paraplegia 4

It regulates the differentiation and development of melanocytes retinal pigment epithelium and is also responsible for pigment cell-specific transcription of the melanogenesis enzyme genes

disease:A chromosomal rearrangement involving CTNNB1 may be a cause of salivary gland pleiomorphic adenomas (PA)

when it is released into the cytoplasm

Mediator containing the CDK8 module is less active than Mediator lacking this module in supporting transcriptional activation

DMRTB Polyclonal Antibody, 100ul Nucleic Acid Isolation & Purification Mutations associated with this gene