DGCR14 Products

Description

This gene is located within the minimal DGS critical region (MDGCR) thought to contain the gene(s) responsible for a group of developmental disorders. These disorders include DiGeorge syndrome, velocardiofacial syndrome, conotruncal anomaly face syndrome, and some familial or sporadic conotruncal cardiac defects which have been associated with microdeletion of 22q11.2. The encoded protein may be a component of C complex spliceosomes, and the orthologous protein in the mouse localizes to the nucleus.

Bioinformatics

Entrez	8220 Human
Uniprot	NP_073210 Human
Product By Gene ID	8220
Alternate Names	DGCR13 DGS-HDGS-I DGSIDGSH DiGeorge syndrome critical region 13 DiGeorge syndrome critical region 14 DiGeorge syndrome critical region gene 13 DiGeorge syndrome critical region gene 14 DiGeorge syndrome gene H DiGeorge syndrome gene I DiGeorge syndrome protein H ES2DiGeorge syndrome critical region gene DGSI Es2el Protein DGCR13 protein DGCR14 Protein ES2

Research Areas for DGCR14

Find related products by research area and learn more about each of the different research areas below.

Neuroscience