adenosine deaminase

Summary
Gene Symbol
  • ADA
Aliases
  • ADA1
Organism
Homo sapiens (human)
NCBI Gene
100
HGNC
186
KEGG Gene ID
PubChem
100
Gene Ontology (GO)
GO Hierarchy
OrthoDB (Group)
Group level
Eukaryota
Group Name
adenosine deaminase
Functional Category
  • E: Amino acid transport and metabolism
  • F: Nucleotide transport and metabolism
  • T: Signal transduction mechanisms
Disease
The Human Phenotype Ontology
Displaying entries 1 - 10 of 69 in total
HPO ID HPO Term
HP:0000007 Autosomal recessive inheritance
HP:0000100 Nephrotic syndrome
HP:0000246 Sinusitis
HP:0000403 Recurrent otitis media
HP:0000821 Hypothyroidism
HP:0000907 Anterior rib cupping
HP:0000926 Platyspondyly
HP:0000944 Abnormal metaphysis morphology
HP:0000958 Dry skin
HP:0000969 Edema
Displaying all 3 entries
Disease ID Disease Name
ORPHA:277
  • severe combined immunodeficiency, autosomal recessive, T cell-negative, B cell-negative, NK cell-negative, due to adenosine deaminase deficiency
OMIM:102700
  • severe combined immunodeficiency, autosomal recessive, T cell-negative, B cell-negative, NK cell-negative, due to adenosine deaminase deficiency
ORPHA:39041
  • Omenn syndrome

About Release Notes Help Feedback

Click here to visit the beta site.


International Collaboration

GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.

Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


Logo License Policies Site Map

Contact: [email protected]

This work is licensed under Creative Commons Attribution 4.0 International


GlyCosmos Portal v4.5.0

Last updated: April 6, 2026