TRPS1 Polyclonal Antibody, 100ul Cell Culture Flasks NBPF7 is a member of

NBPF7 is a member of the neuroblastoma breakpoint family (NBPF) which consists of dozens of recently duplicated genes primarily located in segmental duplications on human chromosome 1

but such a defect has not yet been observed

This gene is a member of the bestrophin gene family of anion channels

|subunit:Interacts with TXNL2/PICOT

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

TRPS1 Polyclonal Antibody, 100ul Cell Culture Flasks NBPF7 is a member ofTRPS1 (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.