Homo sapiens Protein: GATA2
Summary
InnateDB Protein IDBP-383629.4
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol GATA2
Protein Name GATA binding protein 2
Synonyms DCML; IMD21; MONOMAC; NFE1B;
Species Homo sapiens
Ensembl Protein ENSP00000400259
InnateDB Gene IDBG-55213 (GATA2)
Protein Structure
UniProt Annotation
Function Transcriptional activator which regulates endothelin-1 gene expression in endothelial cells. Binds to the consensus sequence 5'-AGATAG-3'.
Subcellular Localization Nucleus.
Disease Associations Immunodeficiency 21 (IMD21) [MIM:614172]: An immunodeficiency disease characterized by profoundly decreased or absent monocytes, B-lymphocytes, natural killer lymphocytes, and circulating and tissue dendritic cells, with little or no effect on T-cell numbers. Clinical features of DCML include susceptibility to disseminated non-tuberculous mycobacterial infections, papillomavirus infections, opportunistic fungal infections, and pulmonary alveolar proteinosis. Bone marrow hypocellularity and dysplasia of myeloid, erythroid, and megakaryocytic lineages are present in most patients, as are karyotypic abnormalities, including monosomy 7 and trisomy 8. This syndrome links susceptibility to mycobacterial, viral, and fungal infections with malignancy and can be transmitted in an autosomal dominant pattern. {ECO:0000269PubMed:21670465}. Note=The disease is caused by mutations affecting the gene represented in this entry.Lymphedema, primary, with myelodysplasia (LMPM) [MIM:614038]: A chronic disabling condition characterized by swelling of the extremities due to altered lymphatic flow, associated with myelodysplasia. Patients with lymphedema suffer from recurrent local infections, and physical impairment. {ECO:0000269PubMed:21892158}. Note=The disease is caused by mutations affecting the gene represented in this entry.Myelodysplastic syndrome (MDS) [MIM:614286]: A heterogeneous group of closely related clonal hematopoietic disorders. All are characterized by a hypercellular or hypocellular bone marrow with impaired morphology and maturation, dysplasia of the myeloid, megakaryocytic and/or erythroid lineages, and peripheral blood cytopenias resulting from ineffective blood cell production. Included diseases are: refractory anemia (RA), refractory anemia with ringed sideroblasts (RARS), refractory anemia with excess blasts (RAEB), refractory cytopenia with multilineage dysplasia and ringed sideroblasts (RCMD-RS); chronic myelomonocytic leukemia (CMML) is a myelodysplastic/myeloproliferative disease. MDS is considered a premalignant condition in a subgroup of patients that often progresses to acute myeloid leukemia (AML). {ECO:0000269PubMed:21892162}. Note=The disease is caused by mutations affecting the gene represented in this entry.
Tissue Specificity Endothelial cells.
Comments
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 39 experimentally validated interaction(s) in this database.
They are also associated with 19 interaction(s) predicted by orthology.
Experimentally validated
Total 45 [view]
Protein-Protein 36 [view]
Protein-DNA 9 [view]
Protein-RNA 0
DNA-DNA 0
RNA-RNA 0
DNA-RNA 0
Predicted by orthology
Total 19 [view]
Gene Ontology

Molecular Function
Accession GO Term
GO:0001158 enhancer sequence-specific DNA binding
GO:0003682 chromatin binding
GO:0003700 sequence-specific DNA binding transcription factor activity
GO:0005515 protein binding
GO:0008134 transcription factor binding
GO:0008270 zinc ion binding
GO:0043565 sequence-specific DNA binding
GO:0070742 C2H2 zinc finger domain binding
Biological Process
GO:0006351 transcription, DNA-templated
GO:0006355 regulation of transcription, DNA-templated
GO:0007596 blood coagulation
GO:0035854 eosinophil fate commitment
GO:0045599 negative regulation of fat cell differentiation
GO:0045746 negative regulation of Notch signaling pathway
GO:0045766 positive regulation of angiogenesis
GO:0045944 positive regulation of transcription from RNA polymerase II promoter
GO:0050766 positive regulation of phagocytosis
GO:0070345 negative regulation of fat cell proliferation
GO:2000178 negative regulation of neural precursor cell proliferation
Cellular Component
GO:0005634 nucleus
GO:0005654 nucleoplasm
Protein Structure and Domains
PDB ID
InterPro IPR000679 Zinc finger, GATA-type
IPR016374 Transcription factor, GATA-1/2/3
PFAM PF00320
PRINTS PR00619
PIRSF PIRSF003027
SMART SM00401
TIGRFAMs
Post-translational Modifications
Modification
Cross-References
SwissProt P23769
PhosphoSite PhosphoSite-P23769
TrEMBL C9J965
UniProt Splice Variant
Entrez Gene 2624
UniGene Hs.709024
RefSeq NP_001139134
HUGO HGNC:4171
OMIM 137295
CCDS CCDS46903
HPRD 00673
IMGT
EMBL AC080005 AK314826 BC002557 BC015577 BC015613 BC018988 BC051272 BC051342 BT006671 CH471052 M68891 M77810
GenPept AAA35868 AAA35869 AAH02557 AAH15577 AAH15613 AAH18988 AAH51272 AAH51342 AAP35317 BAG37347 EAW79313 EAW79314 EAW79315 EAW79316 EAW79317