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MGI:Mll5

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Contents

Species (Taxon ID) Mus musculus (house mouse) (taxon:10090)
Gene Name(s) Mll5 ( synonyms: Kmt2E )
Protein Name(s) myeloid/lymphoid or mixed-lineage leukemia 5,
External Links
MGI MGI:1924825

Annotations

Qualifier GO ID GO term name Reference Evidence Code with/from Aspect Notes Status
GO:0002446

neutrophil mediated immunity

MGI:MGI:3834766
PMID:18854576[1]

IMP: Inferred from Mutant Phenotype

P

From MGI

GO:0003713

transcription coactivator activity

MGI:MGI:4834177

ISO: Inferred from Sequence Orthology

UniProtKB:Q8IZD2

F

From MGI

GO:0005634

nucleus

MGI:MGI:1354194

IEA: Inferred from Electronic Annotation

UniProtKB-KW:KW-0539

C

From MGI

GO:0006306

DNA methylation

MGI:MGI:3834766
PMID:18854576[1]

IMP: Inferred from Mutant Phenotype

P

From MGI

GO:0006351

transcription, DNA-dependent

MGI:MGI:1354194

IEA: Inferred from Electronic Annotation

UniProtKB-KW:KW-0804

P

From MGI

GO:0006355

regulation of transcription, DNA-dependent

MGI:MGI:1354194

IEA: Inferred from Electronic Annotation

UniProtKB-KW:KW-0805

P

From MGI

GO:0007049

cell cycle

MGI:MGI:1354194

IEA: Inferred from Electronic Annotation

UniProtKB-KW:KW-0131

P

From MGI

GO:0007050

cell cycle arrest

MGI:MGI:1354194

IEA: Inferred from Electronic Annotation

UniProtKB-KW:KW-0338

P

From MGI

GO:0008168

methyltransferase activity

MGI:MGI:1354194

IEA: Inferred from Electronic Annotation

UniProtKB-KW:KW-0489

F

From MGI

GO:0008270

zinc ion binding

MGI:MGI:2152098

IEA: Inferred from Electronic Annotation

InterPro:IPR001965

F

From MGI

GO:0016568

chromatin modification

MGI:MGI:1354194

IEA: Inferred from Electronic Annotation

UniProtKB-KW:KW-0156

P

From MGI

GO:0016740

transferase activity

MGI:MGI:1354194

IEA: Inferred from Electronic Annotation

UniProtKB-KW:KW-0808

F

From MGI

GO:0018022

peptidyl-lysine methylation

MGI:MGI:2152096

IEA: Inferred from Electronic Annotation

EC:2.1.1.43

P

From MGI

GO:0018022

peptidyl-lysine methylation

MGI:MGI:4834177

ISO: Inferred from Sequence Orthology

UniProtKB:Q8IZD2

P

From MGI

GO:0018024

histone-lysine N-methyltransferase activity

MGI:MGI:2152096

IEA: Inferred from Electronic Annotation

EC:2.1.1.43

F

From MGI

GO:0019899

enzyme binding

MGI:MGI:4834177

ISO: Inferred from Sequence Orthology

UniProtKB:Q8IZD2

F

From MGI

GO:0030218

erythrocyte differentiation

MGI:MGI:3834766
PMID:18854576[1]

IMP: Inferred from Mutant Phenotype

P

From MGI

GO:0030854

positive regulation of granulocyte differentiation

MGI:MGI:4834177

ISO: Inferred from Sequence Orthology

UniProtKB:Q8IZD2

P

From MGI

GO:0032259

methylation

MGI:MGI:1354194

IEA: Inferred from Electronic Annotation

UniProtKB-KW:KW-0489

P

From MGI

GO:0034968

histone lysine methylation

MGI:MGI:2152096

IEA: Inferred from Electronic Annotation

EC:2.1.1.43

P

From MGI

GO:0042119

neutrophil activation

MGI:MGI:3834766
PMID:18854576[1]

IMP: Inferred from Mutant Phenotype

P

From MGI

GO:0042800

histone methyltransferase activity (H3-K4 specific)

MGI:MGI:4834177

ISO: Inferred from Sequence Orthology

UniProtKB:Q8IZD2

F

From MGI

GO:0045893

positive regulation of transcription, DNA-dependent

MGI:MGI:4834177

ISO: Inferred from Sequence Orthology

UniProtKB:Q8IZD2

P

From MGI

GO:0046872

metal ion binding

MGI:MGI:1354194

IEA: Inferred from Electronic Annotation

UniProtKB-KW:KW-0479

F

From MGI

GO:0048384

retinoic acid receptor signaling pathway

MGI:MGI:4834177

ISO: Inferred from Sequence Orthology

UniProtKB:Q8IZD2

P

From MGI

GO:0051568

histone H3-K4 methylation

MGI:MGI:4834177

ISO: Inferred from Sequence Orthology

UniProtKB:Q8IZD2

P

From MGI

GO:0070688

MLL5-L complex

MGI:MGI:4834177

ISO: Inferred from Sequence Orthology

UniProtKB:Q8IZD2

C

From MGI

GO:0071300

cellular response to retinoic acid

MGI:MGI:4834177

ISO: Inferred from Sequence Orthology

UniProtKB:Q8IZD2

P

From MGI


Notes

References

See Help:References for how to manage references in GONUTS.
  1. 1.0 1.1 1.2 1.3 Heuser M et al. (2009) Loss of MLL5 results in pleiotropic hematopoietic defects, reduced neutrophil immune function, and extreme sensitivity to DNA demethylation. Blood 113: 1432-43 PubMed GONUTS page
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