
GATA2 - Wikipedia
GATA2 or GATA-binding factor 2 is a transcription factor, i.e. a nuclear protein which regulates the expression of genes. [5] . It regulates many genes that are critical for the embryonic …
GATA2deficiency is a rare disorder of the immune system with wide-ranging effects. First identified in 2011, the disorder is char. - acterized by immunodeficiency, myelodys- plastic …
GATA2 deficiency - Wikipedia
GATA2 deficiency is a grouping of several disorders caused by common defect, namely, familial or sporadic inactivating mutations in one of the two parental GATA2 genes. Because the gene …
The spectrum of GATA2 deficiency syndrome | Blood | American ...
2023年3月30日 · Inherited or de novo germ line heterozygous mutations in the gene encoding the transcription factor GATA2 lead to its deficiency. This results in a constellation of clinical …
The Clinical Spectrum, Diagnosis, and Management of GATA2 ...
In this review, we will examine the structural characteristics of the GATA2 gene, its physiological and pathological functions, how GATA2 genetic mutations contribute to myeloid neoplasms, …
GATA2 Gene - GeneCards | GATA2 Protein | GATA2 Antibody
2024年12月25日 · GATA2 (GATA Binding Protein 2) is a Protein Coding gene. Diseases associated with GATA2 include Immunodeficiency 21 and Myelodysplastic Syndrome. Among …
Human GATA2 mutations and hematologic disease: how many …
2020年9月22日 · More than 300 GATA2 variants representing missense, truncating, and noncoding enhancer mutations have been documented. Although these variants can diminish …
GATA2 deficiency syndrome: A decade of discovery - PubMed
GATA2 deficiency syndrome (G2DS) is a rare autosomal dominant genetic disease predisposing to a range of symptoms, of which myeloid malignancy and immunodeficiency including …
GATA2 Deficiency Syndrome (PDQ®) - NCI
2024年8月22日 · GATA2 deficiency syndrome is a hereditary hematologic malignancy syndrome associated with the GATA2 gene. Learn about GATA2's clinical features and management.
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GATA2 deficiency syndrome (G2DS) is a rare autosomal dominant genetic disease predisposing to a range of symptoms of which myeloid malignancy and immunodeficiency including …