PRDM2 Rabbit Polyclonal Antibody, 20ul Gene Synthesis congenital hypothyroidism and Waardenburg syndrome

congenital hypothyroidism and Waardenburg syndrome

Defects in this gene are a cause of branchiooculofacial syndrome (BOFS)

there are multiple processed pseudogenes of RPL11 dispersed through the genome

This gene is a member of the nudix (nucleoside diphosphate linked moiety X)-type motif containing family

GFRA4 is a candidate gene for RET-associated diseases

PRDM2 Rabbit Polyclonal Antibody, 20ul Gene Synthesis congenital hypothyroidism and Waardenburg syndromeThis tumor suppressor gene is a member of a nuclear histone protein methyltransferase superfamily. It encodes a zinc finger protein that can bind to retinoblastoma protein estrogen receptor and the TPA responsive element (MTE) of the heme oxygenase 1 gene. Although the functions of this protein have not been fully characterized it may (1) play a role in transcriptional regulation during neuronal differentiation and pathogenesis of retinoblastoma (2)