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
RS782272214 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS782281934 Health Risk Conflicting classifications of pathogenicity
RS782291827 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS782293850 Health Risk Conflicting classifications of pathogenicity Wiedemann-Steiner syndrome, Wiedemann-Steiner syndrome
RS782302349 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS782313746 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS782359762 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS782373344 Health Risk Conflicting classifications of pathogenicity
RS782407414 Health Risk Conflicting classifications of pathogenicity Wiedemann-Steiner syndrome, Wiedemann-Steiner syndrome
RS782438210 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS782442429 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS782450420 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS782460936 Health Risk Conflicting classifications of pathogenicity
RS782483583 Health Risk Conflicting classifications of pathogenicity Wiedemann-Steiner syndrome, Inborn genetic diseases, Wiedemann-Steiner syndrome
RS782497028 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS782503325 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS782542236 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS782631753 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS782663858 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS782670360 Health Risk Conflicting classifications of pathogenicity
RS782683534 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS782702303 Health Risk Conflicting classifications of pathogenicity KMT2A-related disorder, Inborn genetic diseases, KMT2A-related disorder
RS782705469 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS782707495 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, KMT2A-related disorder, Inborn genetic diseases
RS782725093 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS782739484 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS868991793 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, KMT2A-related disorder, Inborn genetic diseases
RS879253756 Health Risk Conflicting classifications of pathogenicity Bilateral ptosis, Atypical behavior, Neurodevelopmental delay
RS940325244 Health Risk Conflicting classifications of pathogenicity Kabuki syndrome 1, Wiedemann-Steiner syndrome, Kabuki syndrome 1
RS956313303 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS979762842 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS980656132 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS988213215 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS1057519149 Health Risk Likely pathogenic
RS1057519403 Health Risk Likely pathogenic Wiedemann-Steiner syndrome, Wiedemann-Steiner syndrome
RS1057520696 Health Risk Likely pathogenic Inborn genetic diseases, Inborn genetic diseases
RS1064796644 Health Risk Likely pathogenic
RS1064796776 Health Risk Likely pathogenic
RS1064797162 Health Risk Likely pathogenic
RS1085307947 Health Risk Likely pathogenic
RS1131691287 Health Risk Likely pathogenic Wiedemann-Steiner syndrome, Wiedemann-Steiner syndrome
RS1131691365 Health Risk Likely pathogenic
RS1131691433 Health Risk Likely pathogenic Wiedemann-Steiner syndrome, Wiedemann-Steiner syndrome
RS141515578 Health Risk Likely pathogenic Wiedemann-Steiner syndrome, Autism spectrum disorder, Wiedemann-Steiner syndrome
RS1555036478 Health Risk Likely pathogenic
RS1555038083 Health Risk Likely pathogenic
RS1555038115 Health Risk Likely pathogenic Inborn genetic diseases, Inborn genetic diseases, Inborn genetic diseases
RS1555041617 Health Risk Likely pathogenic
RS1555042987 Health Risk Likely pathogenic
RS1555045177 Health Risk Likely pathogenic Wiedemann-Steiner syndrome, Wiedemann-Steiner syndrome
« Prev 1 2 3 4 5 6 ... 11 Next »
Sign Up to Analyze Your DNA Log In