Kmt2a (lysine methyltransferase 2A) - Rat Genome Database

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Gene: Kmt2a (lysine methyltransferase 2A) Rattus norvegicus
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Symbol: Kmt2a
Name: lysine methyltransferase 2A
RGD ID: 1586165
Description: Enables DNA-binding transcription factor binding activity. Involved in several processes, including cellular response to transforming growth factor beta stimulus; membrane depolarization; and response to potassium ion. Predicted to be located in cytosol and nucleoplasm. Predicted to be part of MLL1 complex. Used to study transient cerebral ischemia. Human ortholog(s) of this gene implicated in acute myeloid leukemia; cervical cancer; myelofibrosis; and non-Hodgkin lymphoma. Orthologous to human KMT2A (lysine methyltransferase 2A); PARTICIPATES IN DNA modification pathway; histone modification pathway; INTERACTS WITH 2,3,7,8-tetrachlorodibenzodioxine; 2,3,7,8-Tetrachlorodibenzofuran; 2,4-dinitrotoluene.
Type: protein-coding
RefSeq Status: VALIDATED
Previously known as: histone-lysine N-methyltransferase 2A; histone-lysine N-methyltransferase MLL; lysine (K)-specific methyltransferase 2A; Mixed-lineage leukemia (also acute lymphocytic leukemia 1 or trithorax Drosophila gene); Mixed-lineage leukemia (also acute lymphocytic leukemia 1 or tritorax Drosophila gene); Mll; Mll1; Mll_mapped; myeloid/lymphoid or mixed-lineage leukemia; myeloid/lymphoid or mixed-lineage leukemia (mapped); myeloid/lymphoid or mixed-lineage leukemia (trithorax homolog, Drosophila); myeloid/lymphoid or mixed-lineage leukemia 1
RGD Orthologs
Human
Mouse
Chinchilla
Bonobo
Dog
Squirrel
Pig
Green Monkey
Naked Mole-Rat
Alliance Orthologs
More Info more info ...
Latest Assembly: GRCr8 - GRCr8 Assembly
Position:
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCr8854,013,547 - 54,089,219 (-)NCBIGRCr8
mRatBN7.2845,116,763 - 45,193,320 (-)NCBImRatBN7.2mRatBN7.2
mRatBN7.2 Ensembl845,118,814 - 45,193,181 (-)EnsemblmRatBN7.2 Ensembl
Rnor_6.0849,110,407 - 49,185,872 (-)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_6.0 Ensembl849,114,990 - 49,158,971 (-)EnsemblRnor6.0rn6Rnor6.0
Rnor_5.0847,728,915 - 47,804,551 (-)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.4847,759,175 - 47,834,586 (-)NCBIRGSC3.4RGSC_v3.4rn4RGSC3.4
Celera844,701,780 - 44,782,476 (-)NCBICelera
Cytogenetic Map8q22NCBI
JBrowse: View Region in Genome Browser (JBrowse)
Model


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Original Reference(s)
Kmt2aRatacute myeloid leukemia  ISOKMT2A (Homo sapiens)1625285 RGD 
Kmt2aRatacute myeloid leukemia amelioratesISOKmt2a (Mus musculus)11530086 RGD 
Kmt2aRatacute myeloid leukemia treatmentISOKMT2A (Homo sapiens)155888491human cell line in a mouse modelRGD 
Kmt2aRatcervical cancer  ISOKMT2A (Homo sapiens)9588221human gene in a mouse modelRGD 
Kmt2aRatKidney Reperfusion Injury  ISOKmt2a (Mus musculus)155888490protein:increased expression:kidney (mouse)RGD 
Kmt2aRatmyelofibrosis exacerbatesISOKMT2A (Homo sapiens)156420157DOID:4971DNA:mutations:multiple (human)RGD 
Kmt2aRatnon-Hodgkin lymphoma  ISOKMT2A (Homo sapiens)1625285 RGD 
Kmt2aRatprostate cancer  ISOKMT2A (Homo sapiens)9587761mRNA:decreased expression:prostate gland (human)RGD 
Kmt2aRattransient cerebral ischemia treatmentIMP 155888565 RGD 
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Kmt2aRatautism spectrum disorder  ISOKMT2A (Homo sapiens)8554872ClinVar Annotator: match by term: Autism spectrum disorderClinVarPMID:25741868 and PMID:28492532
Kmt2aRatCD3epsilon deficiency  ISOKMT2A (Homo sapiens)8554872ClinVar Annotator: match by term: CD3epsilon deficiencyClinVarPMID:14602880 more ...
Kmt2aRatchromosome 11 partial duplication syndrome  ISOKMT2A (Homo sapiens)8554872ClinVar Annotator: match by term: Distal trisomy 11qClinVarPMID:25741868
Kmt2aRatCornelia de Lange syndrome 1  ISOKMT2A (Homo sapiens)8554872ClinVar Annotator: match by term: Cornelia de Lange syndrome 1ClinVarPMID:25574841
Kmt2aRatDevelopmental Disease  ISOKMT2A (Homo sapiens)8554872ClinVar Annotator: match by term: Developmental disorderClinVarPMID:25741868
Kmt2aRatDwarfism  ISOKMT2A (Homo sapiens)8554872ClinVar Annotator: match by term: Short statureClinVarPMID:32581362
Kmt2aRatFamilial Atrial Fibrillation 14  ISOKMT2A (Homo sapiens)8554872ClinVar Annotator: match by term: Atrial fibrillation more ...ClinVarPMID:28492532
Kmt2aRatgenetic disease  ISOKMT2A (Homo sapiens)8554872ClinVar Annotator: match by term: Inborn genetic diseasesClinVarPMID:18414213 more ...
Kmt2aRatglycogen storage disease Ib  ISOKMT2A (Homo sapiens)8554872ClinVar Annotator: match by term: Glucose-6-phosphate transport defectClinVarPMID:28492532
Kmt2aRatHirsutism  ISOKMT2A (Homo sapiens)8554872ClinVar Annotator: match by term: HirsutismClinVarPMID:22795537 more ...
Kmt2aRatimmunodeficiency 17  ISOKMT2A (Homo sapiens)8554872ClinVar more ...ClinVarPMID:14602880 more ...
Kmt2aRatimmunodeficiency 18  ISOKMT2A (Homo sapiens)8554872ClinVar Annotator: match by term: Immunodeficiency 18ClinVarPMID:14602880 more ...
Kmt2aRatimmunodeficiency 19  ISOKMT2A (Homo sapiens)8554872ClinVar Annotator: match by term: Immunodeficiency 19ClinVarPMID:14602880 more ...
Kmt2aRatinflammatory bowel disease 28  ISOKMT2A (Homo sapiens)8554872ClinVar Annotator: match by term: Inflammatory bowel disease 28ClinVarPMID:14602880 more ...
Kmt2aRatintellectual disability  ISOKMT2A (Homo sapiens)8554872ClinVar more ...ClinVarPMID:22795537 more ...
Kmt2aRatintellectual disability  ISOKMT2A (Homo sapiens)8554872ClinVar more ...ClinVarPMID:22795537 more ...
Kmt2aRatisolated microphthalmia 5  ISOKMT2A (Homo sapiens)8554872ClinVar Annotator: match by term: Isolated microphthalmia 5ClinVarPMID:28492532
Kmt2aRatKabuki Syndrome 1  ISOKMT2A (Homo sapiens)8554872ClinVar Annotator: match by term: Kabuki syndrome 1ClinVarPMID:25741868 and PMID:29255178
Kmt2aRatlanguage disorder  ISOKMT2A (Homo sapiens)8554872ClinVar Annotator: match by term: Language disorderClinVarPMID:25741868 more ...
Kmt2aRatlong QT syndrome 10  ISOKMT2A (Homo sapiens)8554872ClinVar Annotator: match by term: Long QT syndrome 10ClinVarPMID:28492532
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Original Reference(s)
Kmt2aRatAcute Erythroleukemia  ISOKMT2A (Homo sapiens)11554173CTD Direct Evidence: marker/mechanismCTDPMID:30926971
Kmt2aRatacute lymphoblastic leukemia  ISOKMT2A (Homo sapiens)11554173CTD Direct Evidence: marker/mechanismCTDPMID:24736461 and PMID:25730765
Kmt2aRatacute monocytic leukemia  ISOKMT2A (Homo sapiens)11554173CTD Direct Evidence: marker/mechanismCTDPMID:8282816
Kmt2aRatacute myeloid leukemia  ISOKMT2A (Homo sapiens)11554173CTD Direct Evidence: marker/mechanismCTDPMID:10339604 and PMID:26237430
Kmt2aRatacute myelomonocytic leukemia  ISOKMT2A (Homo sapiens)11554173CTD Direct Evidence: marker/mechanismCTDPMID:8282816
Kmt2aRatadenocarcinoma  ISOKMT2A (Homo sapiens)11554173CTD Direct Evidence: marker/mechanismCTDPMID:22484628
Kmt2aRatChromosome Aberrations  ISOKMT2A (Homo sapiens)11554173CTD Direct Evidence: marker/mechanismCTDPMID:24736461
Kmt2aRathepatocellular carcinoma  ISOKMT2A (Homo sapiens)11554173CTD Direct Evidence: marker/mechanismCTDPMID:22634756
Kmt2aRatleukemia  ISOKMT2A (Homo sapiens)11554173CTD Direct Evidence: marker/mechanismCTDPMID:11731795 and PMID:12937054
Kmt2aRatlung small cell carcinoma  ISOKMT2A (Homo sapiens)11554173CTD Direct Evidence: marker/mechanismCTDPMID:22941188
Kmt2aRatlymphoid leukemia  ISOKMT2A (Homo sapiens)11554173CTD Direct Evidence: marker/mechanismCTDPMID:17463288
Kmt2aRatmyeloid leukemia  ISOKMT2A (Homo sapiens)11554173CTD Direct Evidence: marker/mechanismCTDPMID:8282816 and PMID:17463288
Kmt2aRatNeurodevelopmental Disorders  ISOKMT2A (Homo sapiens)11554173CTD Direct Evidence: marker/mechanismCTDPMID:28191889
Kmt2aRatProstatic Neoplasms  ISOKMT2A (Homo sapiens)11554173CTD Direct Evidence: marker/mechanismCTDPMID:29610475
Kmt2aRatStomach Neoplasms  ISOKMT2A (Homo sapiens)11554173CTD Direct Evidence: marker/mechanismCTDPMID:22484628
Kmt2aRattransitional cell carcinoma  ISOKMT2A (Homo sapiens)11554173CTD Direct Evidence: marker/mechanismCTDPMID:21822268
Kmt2aRaturinary bladder cancer  ISOKMT2A (Homo sapiens)11554173CTD Direct Evidence: marker/mechanismCTDPMID:21822268
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Original Reference(s)
Kmt2aRatacute lymphoblastic leukemia  ISSKmt2a (Mus musculus)13592920OMIM:247640 more ...MouseDO 
Kmt2aRatacute myeloid leukemia  ISSKmt2a (Mus musculus)13592920OMIM:601626MouseDO 
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Original Reference(s)
Kmt2aRatWiedemann-Steiner syndrome  ISOKMT2A (Homo sapiens)7240710 OMIM 

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Original Reference(s)
Kmt2aRat(1->4)-beta-D-glucan multiple interactionsISOKmt2a (Mus musculus)6480464[perfluorooctane sulfonic acid co-treated with Cellulose] results in decreased expression of KMT2A mRNACTDPMID:36331819
Kmt2aRat17beta-estradiol decreases expressionISOKMT2A (Homo sapiens)6480464Estradiol results in decreased expression of KMT2A mRNACTDPMID:19167446
Kmt2aRat2,3,7,8-tetrachlorodibenzodioxine affects expressionISOKmt2a (Mus musculus)6480464Tetrachlorodibenzodioxin affects the expression of KMT2A mRNACTDPMID:18691609
Kmt2aRat2,3,7,8-tetrachlorodibenzodioxine decreases expressionEXP 6480464Tetrachlorodibenzodioxin results in decreased expression of KMT2A mRNACTDPMID:33387578
Kmt2aRat2,3,7,8-tetrachlorodibenzodioxine increases expressionEXP 6480464Tetrachlorodibenzodioxin results in increased expression of KMT2A mRNACTDPMID:34747641
Kmt2aRat2,3,7,8-Tetrachlorodibenzofuran decreases expressionEXP 64804642 more ...CTDPMID:32109520
Kmt2aRat2,4-dinitrotoluene affects expressionEXP 64804642 and 4-dinitrotoluene affects the expression of KMT2A mRNACTDPMID:21346803
Kmt2aRat2,6-dinitrotoluene affects expressionEXP 64804642 and 6-dinitrotoluene affects the expression of KMT2A mRNACTDPMID:21346803
Kmt2aRat2-hydroxypropanoic acid increases expressionISOKMT2A (Homo sapiens)6480464Lactic Acid results in increased expression of KMT2A mRNACTDPMID:30851411
Kmt2aRat4,4'-sulfonyldiphenol decreases methylationISOKmt2a (Mus musculus)6480464bisphenol S results in decreased methylation of KMT2A exonCTDPMID:33297965
Kmt2aRat4,4'-sulfonyldiphenol affects methylationISOKmt2a (Mus musculus)6480464bisphenol S affects the methylation of KMT2A geneCTDPMID:31683443
Kmt2aRat4-octylphenol increases expressionISOKMT2A (Homo sapiens)64804644-octylphenol results in increased expression of KMT2A proteinCTDPMID:20056579
Kmt2aRat6-propyl-2-thiouracil decreases expressionEXP 6480464Propylthiouracil results in decreased expression of KMT2A mRNACTDPMID:30047161
Kmt2aRataflatoxin B1 increases expressionISOKmt2a (Mus musculus)6480464Aflatoxin B1 results in increased expression of KMT2A mRNACTDPMID:19770486
Kmt2aRataflatoxin B1 increases methylationISOKMT2A (Homo sapiens)6480464Aflatoxin B1 results in increased methylation of KMT2A exonCTDPMID:30157460
Kmt2aRatall-trans-retinoic acid decreases expressionISOKMT2A (Homo sapiens)6480464Tretinoin results in decreased expression of KMT2A mRNACTDPMID:22906706 and PMID:33167477
Kmt2aRatalpha-Zearalanol multiple interactionsEXP 6480464[Zeranol co-treated with perfluorooctanoic acid] results in decreased expression of KMT2A mRNACTDPMID:35163327
Kmt2aRatamitrole decreases expressionEXP 6480464Amitrole results in decreased expression of KMT2A mRNACTDPMID:30047161
Kmt2aRatamphetamine decreases expressionEXP 6480464Amphetamine results in decreased expression of KMT2A mRNACTDPMID:30779732
Kmt2aRatarsenite(3-) multiple interactionsISOKMT2A (Homo sapiens)6480464arsenite inhibits the reaction [G3BP1 protein binds to KMT2A mRNA]CTDPMID:32406909

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Biological Process
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Original Reference(s)
Kmt2aRatanterior/posterior pattern specification acts_upstream_of_or_withinIEAUniProtKB:P55200 and ensembl:ENSMUSP000001103371600115GO_REF:0000107EnsemblGO_REF:0000107
Kmt2aRatanterior/posterior pattern specification acts_upstream_of_or_withinISOKmt2a (Mus musculus)1624291MGI:1932339 PMID:15741318 and PMID:16618927RGDPMID:15741318 and PMID:16618927
Kmt2aRatcellular response to transforming growth factor beta stimulus  IMP 155888490 RGD 
Kmt2aRatchromatin organization involved_inIEAUniProtKB-KW:KW-01561600115GO_REF:0000043UniProtGO_REF:0000043
Kmt2aRatcircadian regulation of gene expression involved_inIEAUniProtKB:P55200 and ensembl:ENSMUSP000001103371600115GO_REF:0000107EnsemblGO_REF:0000107
Kmt2aRatcircadian regulation of gene expression involved_inISOKmt2a (Mus musculus)1624291 PMID:21113167RGDPMID:21113167
Kmt2aRatcognition acts_upstream_of_or_withinISOKmt2a (Mus musculus)1624291MGI:3839794 PMID:25834037RGDPMID:25834037
Kmt2aRatcognition acts_upstream_of_or_withinIEAUniProtKB:P55200 and ensembl:ENSMUSP000001103371600115GO_REF:0000107EnsemblGO_REF:0000107
Kmt2aRatdefinitive hemopoiesis involved_inIEAUniProtKB:P55200 and ensembl:ENSMUSP000001103371600115GO_REF:0000107EnsemblGO_REF:0000107
Kmt2aRatdefinitive hemopoiesis involved_inISOKmt2a (Mus musculus)1624291 PMID:15556871RGDPMID:15556871
Kmt2aRatembryonic hemopoiesis acts_upstream_of_or_withinISOKmt2a (Mus musculus)1624291MGI:2177818 PMID:9639506RGDPMID:9639506
Kmt2aRatembryonic hemopoiesis acts_upstream_of_or_withinIEAUniProtKB:P55200 and ensembl:ENSMUSP000001103371600115GO_REF:0000107EnsemblGO_REF:0000107
Kmt2aRatepigenetic regulation of gene expression acts_upstream_of_or_withinIEAUniProtKB:P55200 and ensembl:ENSMUSP000001103371600115GO_REF:0000107EnsemblGO_REF:0000107
Kmt2aRatepigenetic regulation of gene expression acts_upstream_of_or_withinISOKmt2a (Mus musculus)1624291 PMID:16618927RGDPMID:16618927
Kmt2aRatexploration behavior acts_upstream_of_or_withinIEAUniProtKB:P55200 and ensembl:ENSMUSP000001103371600115GO_REF:0000107EnsemblGO_REF:0000107
Kmt2aRatexploration behavior acts_upstream_of_or_withinISOKmt2a (Mus musculus)1624291MGI:3839794 PMID:25834037RGDPMID:25834037
Kmt2aRatfibroblast proliferation acts_upstream_ofISOKmt2a (Mus musculus)1624291 PMID:15640349RGDPMID:15640349
Kmt2aRatfibroblast proliferation acts_upstream_ofIEAUniProtKB:P55200 and ensembl:ENSMUSP000001103371600115GO_REF:0000107EnsemblGO_REF:0000107
Kmt2aRathomeostasis of number of cells within a tissue acts_upstream_of_or_withinISOKmt2a (Mus musculus)1624291MGI:95559 PMID:22674806RGDPMID:22674806
Kmt2aRathomeostasis of number of cells within a tissue acts_upstream_of_or_withinIEAUniProtKB:P55200 and ensembl:ENSMUSP000001103371600115GO_REF:0000107EnsemblGO_REF:0000107
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Cellular Component
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Kmt2aRatcytosol located_inISOKMT2A (Homo sapiens) more ...1624291 RGDGO_REF:0000052
Kmt2aRatcytosol located_inIEAUniProtKB:Q03164 and ensembl:ENSP000004367861600115GO_REF:0000107EnsemblGO_REF:0000107
Kmt2aRathistone methyltransferase complex part_ofISOKMT2A (Homo sapiens)1624291 PMID:19556245RGDPMID:19556245
Kmt2aRathistone methyltransferase complex part_ofIEAInterPro:IPR0165691600115GO_REF:0000002InterProGO_REF:0000002
Kmt2aRathistone methyltransferase complex part_ofIBAFB:FBgn0003862 more ...1600115GO_REF:0000033GO_CentralGO_REF:0000033
Kmt2aRathistone methyltransferase complex part_ofIEAUniProtKB:Q03164 and ensembl:ENSP000004367861600115GO_REF:0000107EnsemblGO_REF:0000107
Kmt2aRatMLL1 complex part_ofISOKMT2A (Homo sapiens)1624291 PMID:15960975 and PMID:23508102RGDPMID:15960975 and PMID:23508102
Kmt2aRatMLL1 complex part_ofIEAUniProtKB:Q03164 and ensembl:ENSP000004367861600115GO_REF:0000107EnsemblGO_REF:0000107
Kmt2aRatnucleoplasm located_inIEAUniProtKB:Q03164 and ensembl:ENSP000004367861600115GO_REF:0000107EnsemblGO_REF:0000107
Kmt2aRatnucleoplasm located_inISOKMT2A (Homo sapiens) more ...1624291 RGDGO_REF:0000052
Kmt2aRatnucleus located_inIEAUniProtKB-KW:KW-05391600115GO_REF:0000043UniProtGO_REF:0000043
Kmt2aRatnucleus located_inIEAInterPro:IPR003888 and InterPro:IPR0038891600115GO_REF:0000002InterProGO_REF:0000002
Kmt2aRatnucleus located_inIEAUniProtKB:P55200 and ensembl:ENSMUSP000001103371600115GO_REF:0000107EnsemblGO_REF:0000107
Kmt2aRatnucleus located_inIEAUniProtKB:Q03164 and ensembl:ENSP000004367861600115GO_REF:0000107EnsemblGO_REF:0000107
Kmt2aRatnucleus located_inIEAUniProtKB-SubCell:SL-01911600115GO_REF:0000044UniProtGO_REF:0000044
Kmt2aRatnucleus located_inISOKmt2a (Mus musculus)1624291 PMID:11555636 and PMID:16618927RGDPMID:11555636 and PMID:16618927
Kmt2aRatnucleus located_inISOKMT2A (Homo sapiens)1624291 PMID:11313484 more ...RGDPMID:11313484 more ...
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Molecular Function
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Kmt2aRatchromatin binding enablesIEAUniProtKB:P55200 and ensembl:ENSMUSP000001103371600115GO_REF:0000107EnsemblGO_REF:0000107
Kmt2aRatchromatin binding enablesISOKmt2a (Mus musculus)1624291 PMID:15640349RGDPMID:15640349
Kmt2aRatDNA binding enablesISOKmt2a (Mus musculus)1624291 PMID:24824656RGDPMID:24824656
Kmt2aRatDNA binding enablesIEAUniProtKB:P55200 and ensembl:ENSMUSP000001103371600115GO_REF:0000107EnsemblGO_REF:0000107
Kmt2aRatDNA binding enablesIEAInterPro:IPR0028571600115GO_REF:0000002InterProGO_REF:0000002
Kmt2aRatDNA binding enablesIEAUniProtKB-KW:KW-02381600115GO_REF:0000043UniProtGO_REF:0000043
Kmt2aRatDNA-binding transcription factor binding  IPIGata3 (Rattus norvegicus)1598407 RGD 
Kmt2aRathistone H3K4 methyltransferase activity enablesISOKMT2A (Homo sapiens)1624291 PMID:15960975 more ...RGDPMID:15960975 more ...
Kmt2aRathistone H3K4 methyltransferase activity enablesIEAUniRule:UR0003617521600115GO_REF:0000104UniProtGO_REF:0000104
Kmt2aRathistone H3K4 methyltransferase activity enablesIEAInterPro:IPR0165691600115GO_REF:0000002InterProGO_REF:0000002
Kmt2aRathistone H3K4 methyltransferase activity enablesIEAARBA:ARBA000346001600115GO_REF:0000117UniProtGO_REF:0000117
Kmt2aRathistone H3K4 methyltransferase activity enablesIEAUniProtKB:P55200 and ensembl:ENSMUSP000001103371600115GO_REF:0000107EnsemblGO_REF:0000107
Kmt2aRathistone H3K4 methyltransferase activity enablesIEAUniProtKB:Q03164 and ensembl:ENSP000004367861600115GO_REF:0000107EnsemblGO_REF:0000107
Kmt2aRathistone H3K4 methyltransferase activity enablesIBAFB:FBgn0003862 more ...1600115GO_REF:0000033GO_CentralGO_REF:0000033
Kmt2aRathistone H3K4 methyltransferase activity enablesISOKmt2a (Mus musculus)1624291MGI:3839794 PMID:12453418 more ...RGDPMID:12453418 more ...
Kmt2aRathistone H3K4 monomethyltransferase activity enablesIEARHEA:602641600115GO_REF:0000116RHEAGO_REF:0000116
Kmt2aRathistone H3K4 trimethyltransferase activity enablesISOKMT2A (Homo sapiens)1624291 PMID:20861184RGDPMID:20861184
Kmt2aRathistone H3K4 trimethyltransferase activity enablesIEAEC:2.1.1.3541600115GO_REF:0000003UniProtGO_REF:0000003
Kmt2aRathistone H3K4 trimethyltransferase activity enablesIEAUniProtKB:Q03164 and ensembl:ENSP000004367861600115GO_REF:0000107EnsemblGO_REF:0000107
Kmt2aRatidentical protein binding enablesISOKMT2A (Homo sapiens)1624291UniProtKB:Q03164 more ...RGDPMID:10656681 and PMID:11313484
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RGD Manual Annotations


  
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Original Reference(s)
Kmt2aRatDNA modification pathway   ISOKMT2A (Homo sapiens)9479164 RGD 
Kmt2aRathistone modification pathway   ISOKMT2A (Homo sapiens)7242632 RGD 
Kmt2aRathistone modification pathway   ISOKMT2A (Homo sapiens)9479053 RGD 

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Reference Title
Reference Citation
1. Histone methylase MLL1 has critical roles in tumor growth and angiogenesis and its knockdown suppresses tumor growth in vivo. Ansari KI, etal., Oncogene. 2013 Jul 11;32(28):3359-70. doi: 10.1038/onc.2012.352. Epub 2012 Aug 27.
2. Histone lysine methylation dynamics: establishment, regulation, and biological impact. Black JC, etal., Mol Cell. 2012 Nov 30;48(4):491-507. doi: 10.1016/j.molcel.2012.11.006.
3. Phylogenetic-based propagation of functional annotations within the Gene Ontology consortium. Gaudet P, etal., Brief Bioinform. 2011 Sep;12(5):449-62. doi: 10.1093/bib/bbr042. Epub 2011 Aug 27.
4. GATA3 (GATA-Binding Protein 3)/KMT2A (Lysine-Methyltransferase-2A) Complex by Increasing H3K4-3me (Trimethylated Lysine-4 of Histone-3) Upregulates NCX3 (Na+-Ca2+ Exchanger 3) Transcription and Contributes to Ischemic Preconditioning Neuroprotection. Guida N, etal., Stroke. 2021 Nov;52(11):3680-3691. doi: 10.1161/STROKEAHA.121.034637. Epub 2021 Oct 25.
5. Menin is necessary for long term maintenance of meningioma-1 driven leukemia. Libbrecht C, etal., Leukemia. 2021 May;35(5):1405-1417. doi: 10.1038/s41375-021-01146-z. Epub 2021 Feb 4.
6. ZF-CxxC domain-containing proteins, CpG islands and the chromatin connection. Long HK, etal., Biochem Soc Trans. 2013 Jun;41(3):727-40. doi: 10.1042/BST20130028.
7. OMIM Disease Annotation Pipeline OMIM Disease Annotation Pipeline
8. Epigenetic chromatin modifications in the cortical spreading depression. Passaro D, etal., Brain Res. 2010 May 6;1329:1-9. doi: 10.1016/j.brainres.2010.03.001. Epub 2010 Mar 6.
9. GOA pipeline RGD automated data pipeline
10. ClinVar Automated Import and Annotation Pipeline RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
11. Data Import for Chemical-Gene Interactions RGD automated import pipeline for gene-chemical interactions
12. Comprehensive gene review and curation RGD comprehensive gene curation
13. MLL1 and DOT1L cooperate with meningioma-1 to induce acute myeloid leukemia. Riedel SS, etal., J Clin Invest. 2016 Apr 1;126(4):1438-50. doi: 10.1172/JCI80825. Epub 2016 Feb 29.
14. The COMPASS family of histone H3K4 methylases: mechanisms of regulation in development and disease pathogenesis. Shilatifard A Annu Rev Biochem. 2012;81:65-95. doi: 10.1146/annurev-biochem-051710-134100.
15. Inhibition of the H3K4 methyltransferase MLL1/WDR5 complex attenuates renal senescence in ischemia reperfusion mice by reduction of p16INK4a. Shimoda H, etal., Kidney Int. 2019 Nov;96(5):1162-1175. doi: 10.1016/j.kint.2019.06.021. Epub 2019 Aug 1.
16. Rearrangement of the MLL gene in acute lymphoblastic and acute myeloid leukemias with 11q23 chromosomal translocations. Thirman MJ, etal., N Engl J Med. 1993 Sep 23;329(13):909-14.
17. Deregulated expression of selected histone methylases and demethylases in prostate carcinoma. Vieira FQ, etal., Endocr Relat Cancer. 2013 Dec 16;21(1):51-61. doi: 10.1530/ERC-13-0375. Print 2014 Feb.
18. Clinical features and next-generation sequencing landscape of essential thrombocythemia, prefibrotic primary myelofibrosis, and overt fibrotic primary myelofibrosis: a Chinese monocentric retrospective study. Zhang L, etal., J Cancer Res Clin Oncol. 2022 Jun 22. doi: 10.1007/s00432-022-04067-1.
1 to 18 of 18 rows
PMID:9639506   PMID:10656681   PMID:11313484   PMID:11555636   PMID:12453418   PMID:15199122   PMID:15556871   PMID:15640349   PMID:15741318   PMID:15960975   PMID:16618927   PMID:16990798  
PMID:19187761   PMID:19556245   PMID:20010842   PMID:20484083   PMID:20861184   PMID:21113167   PMID:22012064   PMID:22046413   PMID:22674806   PMID:24824656   PMID:25561738   PMID:25834037  
PMID:26324722   PMID:29276034   PMID:29302059  



Kmt2a
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCr8854,013,547 - 54,089,219 (-)NCBIGRCr8
mRatBN7.2845,116,763 - 45,193,320 (-)NCBImRatBN7.2mRatBN7.2
mRatBN7.2 Ensembl845,118,814 - 45,193,181 (-)EnsemblmRatBN7.2 Ensembl
Rnor_6.0849,110,407 - 49,185,872 (-)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_6.0 Ensembl849,114,990 - 49,158,971 (-)EnsemblRnor6.0rn6Rnor6.0
Rnor_5.0847,728,915 - 47,804,551 (-)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.4847,759,175 - 47,834,586 (-)NCBIRGSC3.4RGSC_v3.4rn4RGSC3.4
Celera844,701,780 - 44,782,476 (-)NCBICelera
Cytogenetic Map8q22NCBI
KMT2A
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh3811118,436,492 - 118,526,832 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl11118,436,456 - 118,526,832 (+)EnsemblGRCh38hg38GRCh38
GRCh3711118,307,207 - 118,397,547 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 3611117,812,415 - 117,901,146 (+)NCBINCBI36Build 36hg18NCBI36
Build 3411117,812,414 - 117,901,146NCBI
Celera11115,467,997 - 115,556,730 (+)NCBICelera
Cytogenetic Map11q23.3NCBI
HuRef11114,244,065 - 114,334,229 (+)NCBIHuRef
CHM1_111118,193,852 - 118,284,190 (+)NCBICHM1_1
T2T-CHM13v2.011118,455,794 - 118,546,121 (+)NCBIT2T-CHM13v2.0
Kmt2a
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm39944,714,652 - 44,793,492 (-)NCBIGRCm39GRCm39mm39
GRCm39 Ensembl944,714,652 - 44,792,594 (-)EnsemblGRCm39 Ensembl
GRCm38944,803,355 - 44,881,352 (-)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl944,803,355 - 44,881,296 (-)EnsemblGRCm38mm10GRCm38
MGSCv37944,611,438 - 44,689,357 (-)NCBIGRCm37MGSCv37mm9NCBIm37
MGSCv36944,554,350 - 44,632,269 (-)NCBIMGSCv36mm8
Celera942,068,287 - 42,146,334 (-)NCBICelera
Cytogenetic Map9A5.2NCBI
cM Map924.84NCBI
Kmt2a
(Chinchilla lanigera - long-tailed chinchilla)
Chinchilla AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChiLan1.0 EnsemblNW_00495541219,586,141 - 19,665,527 (+)EnsemblChiLan1.0
ChiLan1.0NW_00495541219,586,435 - 19,670,149 (+)NCBIChiLan1.0ChiLan1.0
KMT2A
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
NHGRI_mPanPan1-v29119,139,884 - 119,230,967 (+)NCBINHGRI_mPanPan1-v2
NHGRI_mPanPan111120,244,773 - 120,335,992 (+)NCBINHGRI_mPanPan1
Mhudiblu_PPA_v011113,273,198 - 113,364,404 (+)NCBIMhudiblu_PPA_v0Mhudiblu_PPA_v0panPan3
PanPan1.111117,203,337 - 117,294,755 (+)NCBIpanpan1.1PanPan1.1panPan2
PanPan1.1 Ensembl11117,204,820 - 117,290,100 (+)Ensemblpanpan1.1panPan2
KMT2A
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.1515,212,559 - 15,302,825 (-)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
CanFam3.1 Ensembl515,217,348 - 15,270,971 (-)EnsemblCanFam3.1canFam3CanFam3.1
Dog10K_Boxer_Tasha515,263,739 - 15,351,690 (-)NCBIDog10K_Boxer_Tasha
ROS_Cfam_1.0515,154,723 - 15,242,720 (-)NCBIROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl515,155,965 - 15,242,720 (-)EnsemblROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.1515,293,171 - 15,381,085 (-)NCBIUMICH_Zoey_3.1
UNSW_CanFamBas_1.0515,196,657 - 15,284,731 (-)NCBIUNSW_CanFamBas_1.0
UU_Cfam_GSD_1.0515,237,660 - 15,325,572 (-)NCBIUU_Cfam_GSD_1.0
Kmt2a
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HiC_Itri_2NW_024404947100,558,662 - 100,644,258 (+)NCBIHiC_Itri_2
SpeTri2.0 EnsemblNW_0049365423,391,774 - 3,562,147 (+)EnsemblSpeTri2.0SpeTri2.0 Ensembl
SpeTri2.0NW_0049365423,480,071 - 3,566,823 (+)NCBISpeTri2.0SpeTri2.0SpeTri2.0
KMT2A
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1 Ensembl945,743,397 - 45,824,884 (+)EnsemblSscrofa11.1susScr11Sscrofa11.1
Sscrofa11.1945,743,566 - 45,828,559 (+)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
Sscrofa10.2950,878,276 - 50,914,778 (-)NCBISscrofa10.2Sscrofa10.2susScr3
KMT2A
(Chlorocebus sabaeus - green monkey)
Green Monkey AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.11109,819,748 - 109,912,763 (+)NCBIChlSab1.1ChlSab1.1chlSab2
ChlSab1.1 Ensembl1109,853,758 - 109,908,113 (+)EnsemblChlSab1.1ChlSab1.1 EnsemblchlSab2
Vero_WHO_p1.0NW_02366604316,125,381 - 16,218,277 (-)NCBIVero_WHO_p1.0Vero_WHO_p1.0
Kmt2a
(Heterocephalus glaber - naked mole-rat)
Naked Mole-Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HetGla_female_1.0 EnsemblNW_00462478413,824,541 - 13,908,077 (+)EnsemblHetGla_female_1.0HetGla_female_1.0 EnsemblhetGla2
HetGla 1.0NW_00462478413,824,507 - 13,912,672 (+)NCBIHetGla_female_1.0HetGla 1.0hetGla2

.

.
Variants in Kmt2a
180 total Variants

Predicted Target Of
Summary Value
Count of predictions:84
Count of miRNA genes:73
Interacting mature miRNAs:75
Transcripts:ENSRNOT00000020573
Prediction methods:Microtar, Miranda, Rnahybrid, Targetscan
Result types:miRGate_prediction

The detailed report is available here: Full Report CSV TAB Printer

miRNA Target Status data imported from miRGate (http://mirgate.bioinfo.cnio.es/).
For more information about miRGate, see PMID:25858286 or access the full paper here.


1 to 10 of 64 rows
The following QTLs overlap with this region.    Full Report CSV TAB Printer Gviewer
RGD ID
Symbol
Name
LOD
P Value
Trait
Sub Trait
Chr
Start
Stop
Species
1298065Scl16Serum cholesterol level QTL 163.8blood cholesterol amount (VT:0000180)plasma total cholesterol level (CMO:0000585)83085640475856404Rat
1554321Bmd3Bone mineral density QTL 37.90.0001femur mineral mass (VT:0010011)volumetric bone mineral density (CMO:0001553)840952565123900184Rat
1578769Uae31Urinary albumin excretion QTL 313.30.001urine albumin amount (VT:0002871)urine albumin excretion rate (CMO:0000757)830848154101699754Rat
1298079Activ2Activity QTL 29.50.000001voluntary movement trait (VT:0003491)rearing measurement (CMO:0001515)84186687686866876Rat
11556286Cm81Cardiac mass QTL 810.01heart mass (VT:0007028)heart weight to body weight ratio (CMO:0000074)83084815461290444Rat
70161Bp62Blood pressure QTL 622.90.001arterial blood pressure trait (VT:2000000)systolic blood pressure (CMO:0000004)84269268490165460Rat
1578765Klgr1Kidney lesion grade QTL 13.30.0001kidney morphology trait (VT:0002135)organ lesion measurement (CMO:0000677)830848154101699754Rat
1582222Epfw2Epididymal fat weight QTL 23.20.0005epididymal fat pad mass (VT:0010421)epididymal fat pad weight to body weight ratio (CMO:0000658)83173772976737729Rat
1354627Despr14Despair related QTL 140.0056locomotor behavior trait (VT:0001392)amount of experiment time spent in a discrete space in an experimental apparatus (CMO:0000958)8768895552688955Rat
61464Niddm11Non-insulin dependent diabetes mellitus QTL 113.10.001blood insulin amount (VT:0001560)plasma insulin level (CMO:0000342)83558203280582032Rat

1 to 10 of 64 rows
BF397432  
Rat AssemblyChrPosition (strand)SourceJBrowse
mRatBN7.2845,168,205 - 45,168,345 (+)MAPPERmRatBN7.2
Rnor_6.0849,161,843 - 49,161,982NCBIRnor6.0
Rnor_5.0847,780,305 - 47,780,444UniSTSRnor5.0
RGSC_v3.4847,810,648 - 47,810,787UniSTSRGSC3.4
Celera844,753,197 - 44,753,336UniSTS
RH 3.4 Map8450.6UniSTS
Cytogenetic Map8q22UniSTS
Mll1  
Rat AssemblyChrPosition (strand)SourceJBrowse
GRCr8854,051,330 - 54,052,138 (+)Marker Load Pipeline
mRatBN7.2845,154,547 - 45,155,354 (+)MAPPERmRatBN7.2
Rnor_6.0849,148,185 - 49,148,991NCBIRnor6.0
Rnor_5.0847,766,647 - 47,767,453UniSTSRnor5.0
RGSC_v3.4847,796,990 - 47,797,796UniSTSRGSC3.4
Celera844,739,562 - 44,740,368UniSTS
Cytogenetic Map8q22UniSTS




alimentary part of gastrointestinal system
appendage
circulatory system
ectoderm
endocrine system
endoderm
exocrine system
hemolymphoid system
hepatobiliary system
integumental system
mesenchyme
mesoderm
nervous system
renal system
reproductive system
respiratory system
9 11 49 113 91 90 59 25 59 6 218 97 93 45 60 31


1 to 21 of 21 rows
RefSeq Transcripts NM_001108139 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001419940 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017603540 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_039082345 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_039082346 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_039082347 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_039082348 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_063265434 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_063265435 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_063265436 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_063265437 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
GenBank Nucleotide AC095317 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC136866 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CH473975 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  FQ225552 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  FQ230296 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  FQ230992 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  FQ232224 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  FQ233101 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  FQ234118 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  JAXUCZ010000008 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
1 to 21 of 21 rows

Ensembl Acc Id: ENSRNOT00000020573   ⟹   ENSRNOP00000020573
Type: CODING
Position:
Rat AssemblyChrPosition (strand)Source
mRatBN7.2 Ensembl845,118,814 - 45,193,181 (-)Ensembl
Rnor_6.0 Ensembl849,114,990 - 49,158,971 (-)Ensembl
RefSeq Acc Id: NM_001108139   ⟹   NP_001101609
RefSeq Status: VALIDATED
Type: CODING
Position:
Rat AssemblyChrPosition (strand)Source
GRCr8854,013,547 - 54,089,219 (-)NCBI
mRatBN7.2845,116,763 - 45,192,437 (-)NCBI
RefSeq Acc Id: NM_001419940   ⟹   NP_001406869
RefSeq Status: VALIDATED
Type: CODING
Position:
Rat AssemblyChrPosition (strand)Source
GRCr8854,013,547 - 54,089,219 (-)NCBI
mRatBN7.2845,116,763 - 45,192,437 (-)NCBI
RefSeq Acc Id: XM_039082345   ⟹   XP_038938273
Type: CODING
Position:
Rat AssemblyChrPosition (strand)Source
GRCr8854,013,555 - 54,089,191 (-)NCBI
mRatBN7.2845,116,771 - 45,193,319 (-)NCBI
RefSeq Acc Id: XM_039082346   ⟹   XP_038938274
Type: CODING
Position:
Rat AssemblyChrPosition (strand)Source
GRCr8854,013,555 - 54,089,191 (-)NCBI
mRatBN7.2845,116,771 - 45,193,320 (-)NCBI
RefSeq Acc Id: XM_039082347   ⟹   XP_038938275
Type: CODING
Position:
Rat AssemblyChrPosition (strand)Source
GRCr8854,013,555 - 54,089,191 (-)NCBI
mRatBN7.2845,116,771 - 45,193,320 (-)NCBI
RefSeq Acc Id: XM_039082348   ⟹   XP_038938276
Type: CODING
Position:
Rat AssemblyChrPosition (strand)Source
GRCr8854,013,555 - 54,089,191 (-)NCBI
mRatBN7.2845,116,771 - 45,193,319 (-)NCBI
RefSeq Acc Id: XM_063265434   ⟹   XP_063121504
Type: CODING
Position:
Rat AssemblyChrPosition (strand)Source
GRCr8854,013,555 - 54,089,191 (-)NCBI
RefSeq Acc Id: XM_063265435   ⟹   XP_063121505
Type: CODING
Position:
Rat AssemblyChrPosition (strand)Source
GRCr8854,013,555 - 54,089,191 (-)NCBI
RefSeq Acc Id: XM_063265436   ⟹   XP_063121506
Type: CODING
Position:
Rat AssemblyChrPosition (strand)Source
GRCr8854,013,555 - 54,057,874 (-)NCBI
RefSeq Acc Id: XM_063265437   ⟹   XP_063121507
Type: CODING
Position:
Rat AssemblyChrPosition (strand)Source
GRCr8854,013,555 - 54,089,191 (-)NCBI
1 to 5 of 11 rows
1 to 5 of 11 rows
Ensembl Acc Id: ENSRNOP00000020573   ⟸   ENSRNOT00000020573
RefSeq Acc Id: XP_038938275   ⟸   XM_039082347
- Peptide Label: isoform X3
- UniProtKB: A6J416 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_038938274   ⟸   XM_039082346
- Peptide Label: isoform X2
- UniProtKB: A6J416 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_038938276   ⟸   XM_039082348
- Peptide Label: isoform X6
- UniProtKB: A6J416 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_038938273   ⟸   XM_039082345
- Peptide Label: isoform X1
- UniProtKB: F1M0L3 (UniProtKB/TrEMBL),   A6J416 (UniProtKB/TrEMBL)
Bromo   CXXC-type   PHD-type   Post-SET   SET


eQTL   View at Phenogen
WGCNA   View at Phenogen
Tissue/Strain Expression   View at Phenogen



1 to 40 of 61 rows
Database
Acc Id
Source(s)
BioCyc Gene G2FUF-30699 BioCyc
Ensembl Genes ENSRNOG00000015133 Ensembl, ENTREZGENE, UniProtKB/TrEMBL
Ensembl Transcript ENSRNOT00000020573 ENTREZGENE
  ENSRNOT00000020573.7 UniProtKB/TrEMBL
  ENSRNOT00000140833 ENTREZGENE
Gene3D-CATH 1.20.920.10 UniProtKB/TrEMBL
  2.170.270.10 UniProtKB/TrEMBL
  3.30.160.360 UniProtKB/TrEMBL
  3.30.40.10 UniProtKB/TrEMBL
  6.10.250.2390 UniProtKB/TrEMBL
InterPro Bromodomain UniProtKB/TrEMBL
  Bromodomain-like_sf UniProtKB/TrEMBL
  EPHD UniProtKB/TrEMBL
  FYrich_C UniProtKB/TrEMBL
  FYrich_N UniProtKB/TrEMBL
  KMT2A_2B_SET UniProtKB/TrEMBL
  KMT2A_ePHD UniProtKB/TrEMBL
  KMT2A_PHD1 UniProtKB/TrEMBL
  KMT2A_PHD2 UniProtKB/TrEMBL
  KMT2A_PHD3 UniProtKB/TrEMBL
  MeTrfase_trithorax UniProtKB/TrEMBL
  Post-SET_dom UniProtKB/TrEMBL
  SET_dom UniProtKB/TrEMBL
  SET_dom_sf UniProtKB/TrEMBL
  Znf_CXXC UniProtKB/TrEMBL
  Znf_FYVE_PHD UniProtKB/TrEMBL
  Znf_PHD UniProtKB/TrEMBL
  Znf_PHD-finger UniProtKB/TrEMBL
  Znf_RING/FYVE/PHD UniProtKB/TrEMBL
NCBI Gene 315606 ENTREZGENE
PANTHER HISTONE-LYSINE-N-METHYLTRANSFERASE 2 KMT2 FAMILY MEMBER UniProtKB/TrEMBL
  PTHR45838:SF2 UniProtKB/TrEMBL
Pfam FYRC UniProtKB/TrEMBL
  FYRN UniProtKB/TrEMBL
  PHD UniProtKB/TrEMBL
  SET UniProtKB/TrEMBL
  zf-CXXC UniProtKB/TrEMBL
  zf-HC5HC2H UniProtKB/TrEMBL
PharmGKB MLL RGD
PhenoGen Kmt2a PhenoGen
1 to 40 of 61 rows


Date Current Symbol Current Name Previous Symbol Previous Name Description Reference Status
2016-02-17 Kmt2a  lysine methyltransferase 2A  Kmt2a  lysine (K)-specific methyltransferase 2A  Nomenclature updated to reflect human and mouse nomenclature 1299863 APPROVED
2013-05-15 Kmt2a  lysine (K)-specific methyltransferase 2A  Mll  myeloid/lymphoid or mixed-lineage leukemia (trithorax homolog, Drosophila)  Nomenclature updated to reflect human and mouse nomenclature 1299863 APPROVED
2013-02-27 Mll  myeloid/lymphoid or mixed-lineage leukemia (trithorax homolog, Drosophila)  Mll1  myeloid/lymphoid or mixed-lineage leukemia 1  Nomenclature updated to reflect human and mouse nomenclature 1299863 APPROVED
2008-03-06 Mll1  myeloid/lymphoid or mixed-lineage leukemia 1  Mll  myeloid/lymphoid or mixed-lineage leukemia  Nomenclature updated to reflect human and mouse nomenclature 1299863 APPROVED
2007-04-13   myeloid/lymphoid or mixed-lineage leukemia  Mll  myeloid/lymphoid or mixed-lineage leukemia (mapped)  Name updated 737654 APPROVED
2007-04-11 Mll  myeloid/lymphoid or mixed-lineage leukemia (mapped)  Mll_mapped  myeloid/lymphoid or mixed-lineage leukemia (mapped)  Data merged from RGD:3093 737654 APPROVED
2006-11-19 Mll  myeloid/lymphoid or mixed-lineage leukemia (mapped)      Symbol and Name status set to provisional 70820 PROVISIONAL
2005-11-17 Mll_mapped  myeloid/lymphoid or mixed-lineage leukemia (mapped)      Symbol and Name updated 1556543 APPROVED
2002-06-10 Mll  Mixed-lineage leukemia (also acute lymphocytic leukemia 1 or tritorax Drosophila gene)      Symbol and Name status set to approved 70586 APPROVED