| AgACC | Ag003880 |
| Date | 19-08-2008 |
| Last updated | 14-12-2016 |
| Antigen Name | AML1 |
| Common Name | AML |
| Full Name | Acute myeloid leukemia 1 protein |
| Synonym | Acute myeloid leukemia 1 protein; CBF-alpha 2; Core-binding factor; alpha 2 subunit; Oncogene AML-1; PEA2-alphaB; PEBP2-alpha B; Polyomavirus enhancer-binding protein 2 alpha B subunit; Runt-ralated transcription factor 1; SL3-3 enhancer factor 1 alpha B subunit; SL3-3 enhancer factor 1 alpha B subunit; SL3/AKV core-binding factor alpha B subunit; acute myeloid leukemia 1 gene; acute myeloid leukemia 1 protein (oncogene AML-1), core-binding factor, alpha subunit; aml1 oncogene; core-binding factor, runt domain, alpha subunit 2; core-binding factor, runt domain, alpha subunit 2 (acute myeloid leukemia 1; aml1 oncogene); runt-related transcription factor 1 (acute myeloid leukemia 1; aml1 oncogene); RUNX1; AML1-EVI-1; AMLCR1; CBFA2; EVI-1; PEBP2A2; PEBP2aB
another display format
- Acute myeloid leukemia 1 protein
- CBF-alpha 2
- Core-binding factor
- alpha 2 subunit
- Oncogene AML-1
- PEA2-alphaB
- PEBP2-alpha B
- Polyomavirus enhancer-binding protein 2 alpha B subunit
- Runt-ralated transcription factor 1
- SL3-3 enhancer factor 1 alpha B subunit
- SL3-3 enhancer factor 1 alpha B subunit
- SL3/AKV core-binding factor alpha B subunit
- acute myeloid leukemia 1 gene
- acute myeloid leukemia 1 protein (oncogene AML-1), core-binding factor, alpha subunit
- aml1 oncogene
- core-binding factor, runt domain, alpha subunit 2
- core-binding factor, runt domain, alpha subunit 2 (acute myeloid leukemia 1
- aml1 oncogene)
- runt-related transcription factor 1 (acute myeloid leukemia 1
- aml1 oncogene)
- RUNX1
- AML1-EVI-1
- AMLCR1
- CBFA2
- EVI-1
- PEBP2A2
- PEBP2aB
|
| UniProt ID | Q01196
|
| NCBI Gene ID | 861 |
| GeneCard ID | GC21M034787 |
| SwissProt VARIANT ID | VAR_012128 |
| Comment | Familial platelet disorder with associated myeloid malignancy (FPDMM) - Defects in RUNX1 are the cause of familial platelet disorder with associated myeloid malignancy. FPDMM is an autosomal dominant disease characterized by qualitative and quantitative platelet defects, and propensity to develop acute myelogenous leukemia |
| Annotation | This is a fragment sequence. |
| Isoforms | Ag000361, Ag000362, Ag000363, Ag000364, Ag000365, Ag000366, Ag000367, Ag000368, Ag000369, Ag000370, Ag000371, Ag002021, Ag002022, Ag002023
Alignment of all Isoforms |
| Mutation entries | Ag000607, Ag000608, Ag000609, Ag000610, Ag000611, Ag000612, Ag000613, Ag000614, Ag000615, Ag000616, Ag000617, Ag000618, Ag000619, Ag000620, Ag000621, Ag000622
... Display all entries
Ag000623, Ag000624, Ag000625, Ag000626, Ag000627, Ag000628, Ag000629, Ag000630, Ag000631, Ag000632, Ag000633, Ag000634, Ag000635, Ag000636, Ag000637, Ag000638, Ag000639, Ag000640, Ag000641, Ag000642, Ag000643, Ag000644, Ag000645, Ag000646, Ag000647, Ag000648, Ag000649, Ag000650, Ag000651, Ag000652, Ag000653, Ag000654, Ag000655, Ag003880, Ag003881, Ag003882
View mutation map |
| Predicted HLA binders | |
| Reference sequence | NATAAMKNQVARFNDLRFVGRSGRGKSFTLTITVFTNPPQV |
| Antigen sequence | NATAAMKNQVARFNDLRFVGQSGRGKSFTLTITVFTNPPQV |
|