TBX18 Polyclonal Antibody, 100ul sgRNA Library Construction Mutations in this gene are

Mutations in this gene are associated with Hermansky-Pudlak syndrome type 1

The protein encoded by this gene is a cytoplasmic nonreceptor protein kinase which may function as an intracellular signal transducer in epithelial tissues

The encoded protein has been reported to function as a transcriptional activator of paired-like homeodomain transcription factor 1 (PITX1

Allelic variants of SCN1A are associated with generalized epilepsy with febrile seizures and epileptic encephalopathy

This gene product is the human homolog of mouse Tbx2

TBX18 Polyclonal Antibody, 100ul sgRNA Library Construction Mutations in this gene areTBX18 (T box 18)codes for a member of an evolutionarily conserved family of transcription factors that plays a crucial role in embryonic development. The family is characterized by the presence of the DNA binding T box domain and is divided into five sub families based on sequence conservation in this domain. The encoded protein belongs to the vertebrate specific Tbx1 sub family. The protein acts as a transcriptional repressor by antagonizing