human ADA2 protein

RefSeq NM_177405. Mutations in the ADA2 protein, human genes are associated with Sneddon Syndrome and deficiency of adenosine deaminase 2.

Also Known As:

ADA2 protein, human; ADA2 adenosine deaminase, human; CECR1 protein, human; adenosine deaminase 2, human; cat eye syndrome chromosome region, candidate 1 protein, human

Networked: 1 relevant articles (0 outcomes, 0 trials/studies)

Bio-Agent Context: Research Results

Experts

1.	Aksentijevich, Ivona: 1 article (01/2019)
2.	Arts, Katrijn: 1 article (01/2019)
3.	Hershfield, Michael: 1 article (01/2019)
4.	Meyts, Isabelle: 1 article (01/2019)
5.	Moens, Leen: 1 article (01/2019)

Related Diseases

1.	Vasculitis (Vasculitides) 01/01/2019 - "The residual adenosine deaminase activity in these patients was attributed to adenosine deaminase 2. Human adenosine deaminase type 2 deficiency (DADA2), due to biallelic deleterious mutations in the ADA2 gene, is the first described monogenic type of small- and medium-size vessel vasculitis. "

Related Drugs and Biologics

1.	Adenosine Deaminase