TRPS1 Polyclonal Antibody, 100ul Cell Culture Flasks Defects in this gene are

Defects in this gene are a cause of benign familial neonatal convulsions type 1 (BFNC)

Sex-determining region Y protein is the testis-determining factor (TDF)

|subunit:Interacts with TXNL2/PICOT

but such a defect has not yet been observed

Hexosaminidase B is the beta subunit of the lysosomal enzyme beta-hexosaminidase that

TRPS1 Polyclonal Antibody, 100ul Cell Culture Flasks Defects in this gene areTRPS1 (transcriptional repressor GATA binding 1) encodes a transcription factor that represses GATA regulated genes and binds to a dynein light chain protein. Binding of the encoded protein to the dynein light chain protein affects binding to GATA consensus sequences and suppresses its transcriptional activity. Defects in TRPS1 are a cause of tricho rhino phalangeal syndrome (TRPS) types I III.