Chordin Polyclonal Antibody, 20ul Dry Bath 1| where most DUF1220 domains

1| where most DUF1220 domains are located| have been implicated in a number of developmental and neurogenetic diseases such as microcephaly| macrocephaly| autism| schizophrenia| mental retardation| congenital heart disease| neuroblastoma| and congenital kidney and urinary tract anomalies

It catalyzes the deacetylation of lysine residues in the histone N-terminal tails and represses transcription in large multiprotein complexes with transcriptional co-repressors

This gene encodes a member of the BTB/POZ and zinc finger domain-containing protein family that are involved in the control of gene expression

and mutations in DYRK1B were found to cause abdominal obesity-metabolic syndrome 3

NFKB2/p52 interacts with NFKBIE

Chordin Polyclonal Antibody, 20ul Dry Bath 1| where most DUF1220 domainsThis gene encodes a secreted protein that dorsalizes early vertebrate embryonic tissues by binding to ventralizing TGF beta like bone morphogenetic proteins and sequestering them in latent complexes. The encoded protein may also have roles in organogenesis and during adulthood. It has been suggested that this gene could be a candidate gene for Cornelia de Lange syndrome. Reduced expression of this gene results in enhanced bone regeneration.