Description: | GATA binding protein 2 [Source:MGI Symbol;Acc:MGI:95662] |
Synonyms: | Gata-2 |
Other ID(s): | MGI:95662, ENSMUSG00000015053 |
Protein Accession Numbers: | NP_001342182, XP_006505602, NP_032116 |
Statistics: | ClinVar(1113) gnomAD(874) COSMIC(759) PTM(19) |
∙ Please click the name of species for the protein accession number used in the alignment.
∙ A p letter used as a pointer to positions of post translational modifications in human.
∙ Protein domains illustrated above belong to Homo sapiens (Human).
∙ ClinVar stacked bar chart represents whole protein isoforms of the gene. Please, check the other protein isoforms of the gene below.
∙ If more than one transcripts below are active (with blue background color), it means all the active transcripts have the same sequence.
ENST00000341105 You are here now!
ENST00000430265
ENST00000487848 You are here now!
ENST00000492608
ENST00000498200
NP_001139133 You are here now!
NP_001139134
NP_116027 You are here now!
Pfam Domain filter_list | Domain Name filter_list | Description filter_list | Positions filter_list | Clan filter_list | Clan Name filter_list | Organism filter_list |
---|---|---|---|---|---|---|
NO RESULT FOUND | ||||||
PF00320 | GATA | GATA zinc finger | 349-383 | CL0167 | Zn_Beta_Ribbon | Homo sapiens |
PF00320 | GATA | GATA zinc finger | 295-329 | CL0167 | Zn_Beta_Ribbon | Homo sapiens |
Disease Name filter_list | Disease Category filter_list | DSI* filter_list | DPI** filter_list | ||
---|---|---|---|---|---|
Cartilage Diseases | Musculoskeletal Diseases ; Skin and Connective Tissue Diseases ; | 0.536 | 0.621 | ||
Leukemia, Myelocytic, Acute | Neoplasms ; | 0.536 | 0.621 | ||
Lymphatic Diseases | Hemic and Lymphatic Diseases ; | 0.536 | 0.621 | ||
Lymphedema | Hemic and Lymphatic Diseases ; | 0.536 | 0.621 | ||
Myelodysplasia | N/A | 0.536 | 0.621 | ||
Acute Myeloid Leukemia, M1 | Neoplasms ; | 0.536 | 0.621 | ||
Chondromalacia | Musculoskeletal Diseases ; Skin and Connective Tissue Diseases ; | 0.536 | 0.621 | ||
Cardiovascular Abnormalities | Cardiovascular Diseases ; Congenital, Hereditary, and Neonatal Diseases and Abnormalities ; | 0.536 | 0.621 | ||
Juvenile Myelomonocytic Leukemia | Neoplasms ; Hemic and Lymphatic Diseases ; | 0.536 | 0.621 | ||
Hematologic Neoplasms | Neoplasms ; Hemic and Lymphatic Diseases ; | 0.536 | 0.621 | ||
Craniofacial Abnormalities | Musculoskeletal Diseases ; Congenital, Hereditary, and Neonatal Diseases and Abnormalities ; | 0.536 | 0.621 | ||
Milroy Disease | Hemic and Lymphatic Diseases ; | 0.536 | 0.621 | ||
Acute Myeloid Leukemia (AML-M2) | Neoplasms ; | 0.536 | 0.621 | ||
Hematopoetic Myelodysplasia | Hemic and Lymphatic Diseases ; | 0.536 | 0.621 | ||
Emberger syndrome | N/A | 0.536 | 0.621 | ||
GATA2 Deficiency | N/A | 0.536 | 0.621 | ||
MYELODYSPLASTIC SYNDROME | Hemic and Lymphatic Diseases ; | 0.536 | 0.621 | ||
NO RESULT FOUND |