MeSH Browser

MeSH Supplementary: ADA2 protein, human
Unique ID: C408373
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C408373
Entry Term(s): ADA2 adenosine deaminase, human; CECR1 protein, human; adenosine deaminase 2, human; cat eye syndrome chromosome region, candidate 1 protein, human
Registry Number: EC 3.5.4.4
Previous Indexing: *GROWTH SUBSTANCES (2000-2002)
Heading Mapped to: *Adenosine Deaminase; *Intercellular Signaling Peptides and Proteins
Frequency: 147
Note: RefSeq NM_177405. Mutations in the ADA2 protein, human genes are associated with Sneddon Syndrome and deficiency of adenosine deaminase 2.
Source: Genomics 2000 Mar 15;64(3):277-85
Date of Entry: 2000/05/26
Revision Date: 2022/11/02

ADA2 protein, human MeSH Supplementary Concept Data 2024