ZCHC8 Polyclonal Antibody, 100ul Cytokines Defects in this gene are

Defects in this gene are the cause of an autosomal recessive form of nonsyndromic sensorineural deafness

and thus phosphorylates and inactivates acetyl-CoA carboxylase (ACC) and beta-hydroxy beta-methylglutaryl-CoA reductase (HMGCR)

regulates the formation of F-actin-containing structures through its interaction with the downstream effector proteins

It undergoes tyrosine phosphorylation and associates with the Src homology 2 domain-containing protein (SH2D1A) as well as with SH2 domain-containing phosphatases (SHPs)

Has higher affinity for L-phenylalanine than LAT1 but lower affinity for glutamine and serine

ZCHC8 Polyclonal Antibody, 100ul Cytokines Defects in this gene areMay be involved in pre mRNA splicing.,PTM: Phosphorylated upon DNA damage, probably by ATM or ATR.,Belongs to the ZCCHC8 family.,Contains 1 CCHC type zinc finger.,subunit: Identified in the spliceosome C complex, at least composed of AQR, ASCC3L1, C19orf29, CDC40, CDC5L, CRNKL1, DDX23, DDX41, DDX48, DDX5, DGCR14, DHX35, DHX38, DHX8, EFTUD2, FRG1, GPATC1, HNRPA1, HNRPA2B1, HNRPA3, HNRPC, HNRPF, HNRPH1, HNRPK, HNRPM, HNRPR, HNRPU, KIAA1160, KIAA1604,