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Results for "DGCR14": 1 gene, 2 gene sets

Name

DGCR14 Gene

DiGeorge syndrome critical region gene 14

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. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Dec 2015]

DGCR14 Gene Set

From Pathway Commons Protein-Protein Interactions

interacting proteins for DGCR14 from the Pathway Commons Protein-Protein Interactions dataset.

Nuclear protein DGCR14 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Nuclear protein DGCR14 protein domain from the InterPro Predicted Protein Domain Annotations dataset.