ADA Gene Set

Dataset Pathway Commons Protein-Protein Interactions
Category physical interactions
Type interacting protein
Description adenosine deaminase|This gene encodes an enzyme that catalyzes the hydrolysis of adenosine to inosine. Various mutations have been described for this gene and have been linked to human diseases. Deficiency in this enzyme causes a form of severe combined immunodeficiency disease (SCID), in which there is dysfunction of both B and T lymphocytes with impaired cellular immunity and decreased production of immunoglobulins, whereas elevated levels of this enzyme have been associated with congenital hemolytic anemia. [provided by RefSeq, Jul 2008] (NCBI Entrez Gene Database, 100)
External Link http://www.ncbi.nlm.nih.gov/gene/100
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Genes

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

Symbol Name
ADORA1 adenosine A1 receptor
ADORA2A adenosine A2a receptor
ADORA2B adenosine A2b receptor
DPP4 dipeptidyl-peptidase 4
DRD1 dopamine receptor D1
GRB2 growth factor receptor-bound protein 2
NR3C1 nuclear receptor subfamily 3, group C, member 1 (glucocorticoid receptor)
PIAS2 protein inhibitor of activated STAT, 2
SGCD sarcoglycan, delta (35kDa dystrophin-associated glycoprotein)
TERF2IP telomeric repeat binding factor 2, interacting protein
TINF2 TERF1 (TRF1)-interacting nuclear factor 2
UBC ubiquitin C