Entity Details

Primary name KMT2B_HUMAN
Entity type UniProt
Source Source Link

Details

AccessionQ9UMN6
EntryNameKMT2B_HUMAN
FullNameHistone-lysine N-methyltransferase 2B
TaxID9606
Evidenceevidence at protein level
Length2715
SequenceStatuscomplete
DateCreated2000-12-01
DateModified2021-06-02

Ontological Relatives

GenesKMT2B

GO terms

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GOName
GO:0005634 nucleus
GO:0005654 nucleoplasm
GO:0008270 zinc ion binding
GO:0035097 histone methyltransferase complex
GO:0042800 histone methyltransferase activity (H3-K4 specific)
GO:0044648 histone H3-K4 dimethylation
GO:0045322 unmethylated CpG binding
GO:0045652 regulation of megakaryocyte differentiation
GO:0045893 positive regulation of transcription, DNA-templated
GO:0051568 histone H3-K4 methylation
GO:0097692 histone H3-K4 monomethylation

Subcellular Location

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Subcellular Location
Nucleus

Domains

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DomainNameCategoryType
IPR001214 SET domainDomainDomain
IPR001965 Zinc finger, PHD-typeDomainDomain
IPR002857 Zinc finger, CXXC-typeDomainDomain
IPR003616 Post-SET domainDomainDomain
IPR003888 FY-rich, N-terminalDomainDomain
IPR003889 FY-rich, C-terminalDomainDomain
IPR011011 Zinc finger, FYVE/PHD-typeFamilyHomologous superfamily
IPR013083 Zinc finger, RING/FYVE/PHD-typeFamilyHomologous superfamily
IPR016569 Methyltransferase, trithoraxFamilyFamily
IPR019787 Zinc finger, PHD-fingerDomainDomain
IPR034732 Extended PHD (ePHD) domainDomainDomain
IPR036427 Bromodomain-like superfamilyFamilyHomologous superfamily
IPR041959 KMT2B, ePHD domainDomainDomain

Diseases

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Disease IDSourceNameDescription
617284 OMIMDystonia 28, childhood-onset (DYT28)A form of dystonia, a disorder defined by the presence of sustained involuntary muscle contraction, often leading to abnormal postures. DYT28 is an autosomal dominant, progressive form characterized by onset in the first decade of life and variable severity. Dystonia begins focally in the lower limbs, resulting in gait difficulties, with later progression to other body regions, including the upper limbs, neck, and orofacial region. The disease is caused by variants affecting the gene represented in this entry.

Interactions

39 interactions

InteractorPartnerSourcesPublicationsLink
KMT2B_HUMANZ512B_HUMANBioGRID, MINT15231748 details
KMT2B_HUMANSMAD3_HUMANBioGRID, MINT15231748 details
KMT2B_HUMANATX1_HUMANBioGRID, IntAct16713569 details
KMT2B_HUMANABL1_HUMANIntAct17474147 details
KMT2B_HUMANCRK_HUMANIntAct17474147 details
KMT2B_HUMANFYN_HUMANIntAct17474147 details
KMT2B_HUMANGRB2_HUMANIntAct17474147 details
KMT2B_HUMANNCK1_HUMANIntAct17474147 details
KMT2B_HUMANANXA1_HUMANBioGRID, MINT21900206 details
KMT2B_HUMANANXA7_HUMANBioGRID, MINT21900206 details
KMT2B_HUMANAT1B1_HUMANBioGRID, MINT21900206 details
KMT2B_HUMANNREP_HUMANBioGRID, MINT21900206 details
KMT2B_HUMANCDN1A_HUMANBioGRID, MINT21900206 details
KMT2B_HUMANGRB7_HUMANBioGRID, MINT21900206 details
KMT2B_HUMANPIN1_HUMANBioGRID, MINT21900206 details
KMT2B_HUMANRAP1B_HUMANBioGRID, MINT21900206 details
KMT2B_HUMANRCC1_HUMANBioGRID, MINT21900206 details
KMT2B_HUMANRPP14_HUMANBioGRID, MINT21900206 details
KMT2B_HUMANSEPT8_HUMANBioGRID, MINT21900206 details
KMT2B_HUMANSMN_HUMANBioGRID, MINT21900206 details
KMT2B_HUMANKITH_HUMANBioGRID, MINT21900206 details
KMT2B_HUMANT22D1_HUMANBioGRID, MINT21900206 details
KMT2B_HUMANWDR5_HUMANBioGRID, DIP, IntAct, MINT20305087 22266653 22665483 23995757 24788516 24981860 26186194 27563068 27705803 28514442 details
KMT2B_HUMANP55G_HUMANBioGRID, IntAct25814554 details
KMT2B_HUMANMEN1_HUMANBioGRID, DIP22327296 23995757 24981860 details
KMT2B_HUMANASH2L_HUMANBioGRID, DIP, MINT17500065 20305087 23995757 24981860 26886794 27563068 34079125 details
KMT2B_HUMANRBBP5_HUMANBioGRID, DIP17500065 21502505 23995757 24981860 27563068 31076518 details
KMT2B_HUMANH31_HUMANBioGRID, IntAct23870121 29568061 details
KMT2B_HUMANTOPB1_HUMANUniProt17913746 details
KMT2B_HUMANTRI63_HUMANBioGRID, IntAct31391242 details
KMT2B_HUMANTRI55_HUMANBioGRID, IntAct31391242 details
KMT2B_HUMANSNF5_HUMANBioGRID19221051 details
KMT2B_HUMANH32_HUMANBioGRID22266653 details
KMT2B_HUMANPPIP1_HUMANIntAct17353931 details
KMT2B_HUMANNCOA6_HUMANBioGRID, DIP17021013 19047629 19433796 24981860 details
KMT2B_HUMANDISC1_HUMANIntAct31413325 details
KMT2B_HUMANPAXI1_HUMANBioGRID17500065 24981860 details
KMT2B_HUMANPAGR1_HUMANBioGRID17500065 details
KMT2B_HUMANWDR82_HUMANBioGRID20516061 24981860 details