KMT2A Chromosome 11

Lysine methyltransferase 2A
518 variants 518 Health Risk

Upload your DNA to see your personal genotypes for variants in KMT2A.

What This Gene Does
This gene encodes a transcriptional coactivator that plays an essential role in regulating gene expression during early development and hematopoiesis. The encoded protein contains multiple conserved functional domains. One of these domains, the SET domain, is responsible for its histone H3 lysine 4 (H3K4) methyltransferase activity which mediates chromatin modifications associated with epigenetic transcriptional activation. This protein is processed by the enzyme Taspase 1 into two fragments, MLL-C and MLL-N. These fragments reassociate and further assemble into different multiprotein complexes that regulate the transcription of specific target genes, including many of the HOX genes. Multiple chromosomal translocations involving this gene are the cause of certain acute lymphoid leukemias and acute myeloid leukemias. Alternate splicing results in multiple transcript variants.[provided by RefSeq, Oct 2010]
Gene Info
Gene Group
"PHD finger proteins|Zinc fingers CXXC-type|Histone lysine methyltransferases|Bromodomain containing|SET domain containing"
Locus Type
gene with protein product
Location
11q23.3
Ensembl
ENSG00000118058
Associated Conditions (22)
Inborn genetic diseases
KMT2A-related disorder
Wiedemann-Steiner syndrome
Gastric cancer
Bilateral ptosis
Atypical behavior
Neurodevelopmental delay
Language disorder
Kabuki syndrome 1
Autism spectrum disorder
Intellectual disability
Rubinstein Taybi like syndrome
See cases
Neurodevelopmental disorder
Rare genetic intellectual disability
Microcephaly
Hirsutism
Cornelia de Lange syndrome 1
Adrenal cortex carcinoma
Squamous cell carcinoma of the head and neck
+2 more conditions
Key Variants
All Variants (518)
RSID Category Clinical Significance Conditions
RS1064797056 Health Risk Conflicting classifications of pathogenicity
RS1259638674 Health Risk Conflicting classifications of pathogenicity
RS1290276055 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS1315427088 Health Risk Conflicting classifications of pathogenicity
RS1317712293 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS1342425133 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS1385508131 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS1388016179 Health Risk Conflicting classifications of pathogenicity KMT2A-related disorder, Wiedemann-Steiner syndrome, KMT2A-related disorder
RS138969270 Health Risk Conflicting classifications of pathogenicity KMT2A-related disorder, KMT2A-related disorder
RS139366882 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS139450035 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS1401608038 Health Risk Conflicting classifications of pathogenicity
RS142658261 Health Risk Conflicting classifications of pathogenicity KMT2A-related disorder, Inborn genetic diseases, KMT2A-related disorder
RS143780031 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS143998546 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS144180211 Health Risk Conflicting classifications of pathogenicity
RS144235455 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS1443122959 Health Risk Conflicting classifications of pathogenicity Wiedemann-Steiner syndrome, Wiedemann-Steiner syndrome
RS1443235781 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS144844866 Health Risk Conflicting classifications of pathogenicity Wiedemann-Steiner syndrome, Inborn genetic diseases, Wiedemann-Steiner syndrome
RS145028869 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS1458634194 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS147844226 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS1479477078 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, KMT2A-related disorder, Inborn genetic diseases
RS150277124 Health Risk Conflicting classifications of pathogenicity
RS150328852 Health Risk Conflicting classifications of pathogenicity KMT2A-related disorder, KMT2A-related disorder
RS150412512 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS1555036085 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS1555036397 Health Risk Conflicting classifications of pathogenicity Wiedemann-Steiner syndrome, Wiedemann-Steiner syndrome
RS1555044758 Health Risk Conflicting classifications of pathogenicity Wiedemann-Steiner syndrome, Wiedemann-Steiner syndrome
RS1555046094 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS1555046152 Health Risk Conflicting classifications of pathogenicity Wiedemann-Steiner syndrome, Inborn genetic diseases, Wiedemann-Steiner syndrome
RS1555047011 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS1555047466 Health Risk Conflicting classifications of pathogenicity Wiedemann-Steiner syndrome, Wiedemann-Steiner syndrome
RS1555138791 Health Risk Conflicting classifications of pathogenicity
RS1565319164 Health Risk Conflicting classifications of pathogenicity
RS1591312470 Health Risk Conflicting classifications of pathogenicity
RS184820566 Health Risk Conflicting classifications of pathogenicity
RS188435877 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS191014566 Health Risk Conflicting classifications of pathogenicity
RS1950106455 Health Risk Conflicting classifications of pathogenicity Wiedemann-Steiner syndrome, Wiedemann-Steiner syndrome
RS1950436398 Health Risk Conflicting classifications of pathogenicity Wiedemann-Steiner syndrome, Wiedemann-Steiner syndrome
RS1950519775 Health Risk Conflicting classifications of pathogenicity
RS1950921220 Health Risk Conflicting classifications of pathogenicity
RS199922480 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS200600434 Health Risk Conflicting classifications of pathogenicity
RS201765973 Health Risk Conflicting classifications of pathogenicity
RS201869352 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS2134268457 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS2134381992 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
1 2 3 4 ... 11 Next »
Sign Up to Analyze Your DNA Log In