DGCR14 Products

Description

DGCR14, also known as DiGeorge syndrome critical region 14, is a 52.6 kDa, 476 amino acid protein that exists in the region thought to be responsible for multiple developmental disorders. Current research is studying the involvement of the protein in diseases and disorders such as DiGeorge syndrome, schizophrenia, velocardiofacial syndrome, and faces syndrome. The protein may be involved in mRNA splicing pathways where it interacts with PFDN1, VIM, TTC14, GNB2L1, and FRA10AC1.

Bioinformatics

Entrez	8220 Human
Uniprot	NP_073210 Human AAH37829.1 Human
Product By Gene ID	8220
Alternate Names	Protein ES2 DiGeorge syndrome protein H protein DGCR14 DiGeorge syndrome critical region 14 Protein DGCR13 DiGeorge syndrome critical region 13 DiGeorge syndrome gene I DiGeorge syndrome critical region gene 13 DiGeorge syndrome gene H Es2el ES2DiGeorge syndrome critical region gene DGSI DGS-HDGS-I DGSIDGSH DGCR13 DiGeorge syndrome critical region gene 14

Diseases related to DGCR14

Discover more about diseases related to DGCR14.

Digeorge Syndrome
Conotruncal Heart Malformations (disorder)
Schizophrenia
22q11 Deletion Syndrome
Nervousness
Schizoaffective Disorder
Craniofacial Abnormalities
Loss Of Chromosome 22
Dissection Of Aorta
Haploinsufficiency
Congenital Heart Defects
Cat Eye Syndrome
Hypoplasia
Dysequilibrium Syndrome
Bipolar Disorder

Pathways for DGCR14

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Pathogenesis

Research Areas for DGCR14

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Neuroscience

Bioinformatics Tool for DGCR14

Discover related pathways, diseases and genes to DGCR14. Need help? Read the Bioinformatics Tool Guide for instructions on using this tool.