RUNX1 gene homepage

General information
Gene symbol RUNX1
Gene name RUNX family transcription factor 1
Chromosome 21
Chromosomal band q22.12
Imprinted Unknown
Genomic reference LRG_482
Transcript reference NM_001001890.2, NM_001122607.1, NM_001754.4
Associated with diseases AML, FPDMM
Citation reference(s) -
Curators (1) Despoina Kalfakakou
Total number of public variants reported 79
Unique public DNA variants reported 29
Individuals with public variants 84
Hidden variants 0
Date created May 20, 2020
Date last updated May 20, 2020
Version RUNX1:200520

Graphical displays and utilities
Graphs Graphs displaying summary information of all variants in the database »
UCSC Genome Browser Show variants in the UCSC Genome Browser (full view, compact view)
Ensembl Genome Browser Show variants in the Ensembl Genome Browser (full view, compact view)
NCBI Sequence Viewer Show distribution histogram of variants in the NCBI Sequence Viewer

Links to other resources
HGNC 10471
Entrez Gene 861
PubMed articles RUNX1
OMIM - Gene 151385
OMIM - Diseases AML (Acute Myeloid Leukemia)
FPDMM (Platelet disorder, familial, with associated myeloid malignancy)

Active transcripts




NCBI ID     

NCBI Protein ID     

00000191 21 runt-related transcription factor 1, transcript variant 1 NM_001754.4 NP_001745.2 79
00000189 21 runt-related transcription factor 1, transcript variant 2 NM_001001890.2 NP_001001890.1 70
00000190 21 runt-related transcription factor 1, transcript variant 3 NM_001122607.1 NP_001116079.1 62

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