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Gene : ADA2 Homo sapiens

Name  ? adenosine deaminase 2 Cytological Location  22q11.1
Brief Description  adenosine deaminase 2
description  This gene encodes a member of a subfamily of the adenosine deaminase protein family. The encoded protein is one of two adenosine deaminases found in humans, which regulate levels of the signaling molecule, adenosine. The encoded protein is secreted from monocytes undergoing differentiation and may regulate cell proliferation and differentiation. This gene may be responsible for some of the phenotypic features associated with cat eye syndrome. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Aug 2013]
  • synonyms:
  • HGNC:1839,
  • VAIHS,
  • cat eye syndrome chromosome region, candidate 1,
  • PAN,
  • ADGF,
  • AF190746,
  • ADA2,
  • ADGF,
  • SNEDS,
  • CECR1,
  • IDGFL,
  • uc062bga.1,
  • NM_001282225,
  • OTTHUMG00000030726,
  • IDGFL,
  • CECR1
  • identifiers:
  • 51816,
  • ENSG00000093072,
  • ADA2

Genome feature

Region: gene ? Length: 43065  
Location: 22:17178790-17221854 reverse strand Cyto location: 22q11.1


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Genomics

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Proteins

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SNPs

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Disease

2 Diseases

Gene (Hum OR Rat) --> Mouse Allele (Phenotype)

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Gene -> HPO annotation (Human Phenotype Ontology)

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Expression

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Other

2011 SN Ps

5 Cross References

18 Data Sets

10 Homologues

0 Located Features

90 Rna Seq Results