NOD1 Rabbit Polyclonal Antibody, 100ul Human Genome Knockout Libraries Variations in this gene have

Variations in this gene have been associated with the hair disorders pseudofolliculitis barbae (PFB) and loose anagen hair syndrome (LAHS)

It is also reported that the this protein functions as a demethylase to activate transcription| as DNA methylation causes gene silencing

structure and integrity

Naturally occurring read-through transcription also exists between ATP5J2 and the downstream pentatricopeptide repeat domain 1 (PTCD1) gene

leucine-rich motif of approximately 60 aa originally found within a subfamily of zinc finger proteins

NOD1 Rabbit Polyclonal Antibody, 100ul Human Genome Knockout Libraries Variations in this gene haveThis gene encodes a member of the NOD (nucleotide binding oligomerization domain) family. This member is a cytosolic protein. It contains an N terminal caspase recruitment domain (CARD) a centrally located nucleotide binding domain (NBD) and 10 tandem leucine rich repeats (LRRs) in its C terminus. The CARD is involved in apoptotic signaling LRRs participate in protein protein interactions and mutations in the NBD may affect the process of