×
Entrez Id:
2624
Gene Symbol:
GATA2
GATA2
0.800
GeneticVariation
disease
CLINVAR
Mutations in GATA2 cause human NK cell deficiency with specific loss of the CD56(bright) subset.
23365458
2013
×
Entrez Id:
2624
Gene Symbol:
GATA2
GATA2
0.800
CausalMutation
disease
CLINVAR
Characterisation of a compound in-cis GATA2 germline mutation in a pedigree presenting with myelodysplastic syndrome/acute myeloid leukemia with concurrent thrombocytopenia.
25676417
2015
×
Entrez Id:
2624
Gene Symbol:
GATA2
GATA2
0.800
GeneticVariation
disease
CLINVAR
Diffuse parenchymal lung disease as first clinical manifestation of GATA-2 deficiency in childhood.
25879889
2015
×
Entrez Id:
2624
Gene Symbol:
GATA2
GATA2
0.800
GeneticVariation
disease
CLINVAR
Genetic features of myelodysplastic syndrome and aplastic anemia in pediatric and young adult patients.
27418648
2016
×
Entrez Id:
2624
Gene Symbol:
GATA2
GATA2
0.800
CausalMutation
disease
CLINVAR
GATA2 haploinsufficiency caused by mutations in a conserved intronic element leads to MonoMAC syndrome.
23502222
2013
×
Entrez Id:
2624
Gene Symbol:
GATA2
GATA2
0.800
CausalMutation
disease
CLINVAR
Mutations in GATA2 cause human NK cell deficiency with specific loss of the CD56(bright) subset.
23365458
2013
×
Entrez Id:
2624
Gene Symbol:
GATA2
GATA2
0.800
CausalMutation
disease
CLINVAR
Mutations in GATA2 cause primary lymphedema associated with a predisposition to acute myeloid leukemia (Emberger syndrome).
21892158
2011
×
Entrez Id:
2624
Gene Symbol:
GATA2
GATA2
0.800
GeneticVariation
disease
CLINVAR
Clinical efficacy of a next-generation sequencing gene panel for primary immunodeficiency diagnostics.
29077208
2018
×
Entrez Id:
2624
Gene Symbol:
GATA2
GATA2
0.800
GeneticVariation
disease
CLINVAR
Acquired ASXL1 mutations are common in patients with inherited GATA2 mutations and correlate with myeloid transformation.
24077845
2014
×
Entrez Id:
2624
Gene Symbol:
GATA2
GATA2
0.800
CausalMutation
disease
CLINVAR
Multiple Opportunistic Infections in a Woman with GATA2 Mutation.
27894982
2017
×
Entrez Id:
2624
Gene Symbol:
GATA2
GATA2
0.800
GeneticVariation
disease
CLINVAR
GATA2 haploinsufficiency caused by mutations in a conserved intronic element leads to MonoMAC syndrome.
23502222
2013
×
Entrez Id:
2624
Gene Symbol:
GATA2
GATA2
0.800
GeneticVariation
disease
CLINVAR
Abstracts of the UK PIN (Primary Immunodeficiency Network) Meeting. December 6-7, 2013. Liverpool, United Kingdom.
24266605
2013
×
Entrez Id:
2624
Gene Symbol:
GATA2
GATA2
0.800
GeneticVariation
disease
CLINVAR
Single-gene association between GATA-2 and autoimmune hepatitis: A novel genetic insight highlighting immunologic pathways to disease.
26812071
2016
×
Entrez Id:
2624
Gene Symbol:
GATA2
GATA2
0.800
GeneticVariation
disease
CLINVAR
Genomic analysis of germ line and somatic variants in familial myelodysplasia/acute myeloid leukemia.
26492932
2015
×
Entrez Id:
2624
Gene Symbol:
GATA2
GATA2
0.800
GeneticVariation
disease
CLINVAR
Prevalence, clinical characteristics, and prognosis of GATA2-related myelodysplastic syndromes in children and adolescents.
26702063
2016
×
Entrez Id:
2624
Gene Symbol:
GATA2
GATA2
0.800
CausalMutation
disease
CLINVAR
Mutations in GATA2 are associated with the autosomal dominant and sporadic monocytopenia and mycobacterial infection (MonoMAC) syndrome .
21670465
2011
×
Entrez Id:
2624
Gene Symbol:
GATA2
GATA2
0.800
GeneticVariation
disease
CLINVAR
Mutations in GATA2 cause primary lymphedema associated with a predisposition to acute myeloid leukemia (Emberger syndrome).
21892158
2011
×
Entrez Id:
2624
Gene Symbol:
GATA2
GATA2
0.800
Biomarker
disease
CTD_human
×
Entrez Id:
2624
Gene Symbol:
GATA2
GATA2
0.800
GermlineCausalMutation
disease
ORPHANET
Mutations in GATA2 are associated with the autosomal dominant and sporadic monocytopenia and mycobacterial infection (MonoMAC) syndrome .
21670465
2011
×
Entrez Id:
2624
Gene Symbol:
GATA2
GATA2
0.800
GermlineCausalMutation
disease
ORPHANET
Exome sequencing identifies GATA-2 mutation as the cause of dendritic cell, monocyte, B and NK lymphoid deficiency .
21765025
2011
×
Entrez Id:
2624
Gene Symbol:
GATA2
GATA2
0.800
GeneticVariation
disease
UNIPROT
Mutations in GATA2 are associated with the autosomal dominant and sporadic monocytopenia and mycobacterial infection (MonoMAC) syndrome .
21670465
2011
×
Entrez Id:
2624
Gene Symbol:
GATA2
GATA2
0.800
Biomarker
disease
GENOMICS_ENGLAND
Natural history of GATA2 deficiency in a survey of 79 French and Belgian patients.
29724903
2018
×
Entrez Id:
2624
Gene Symbol:
GATA2
GATA2
0.800
Biomarker
disease
GENOMICS_ENGLAND
Heritable GATA2 mutations associated with familial myelodysplastic syndrome and acute myeloid leukemia.
21892162
2011
×
Entrez Id:
2624
Gene Symbol:
GATA2
GATA2
0.800
Biomarker
disease
GENOMICS_ENGLAND
×
Entrez Id:
2624
Gene Symbol:
GATA2
GATA2
0.800
Biomarker
disease
GENOMICS_ENGLAND
Genetic features of myelodysplastic syndrome and aplastic anemia in pediatric and young adult patients.
27418648
2016