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EntrezGene:8085: Difference between revisions

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{{EntrezGene
{{EntrezGene
|tax_id=9606
|Full_name_from_nomenclature_authority=myeloid/lymphoid or mixed-lineage leukemia 2
|GeneID=8085
|GeneID=8085
|LocusTag=-
|Modification_date=20120108
|Nomenclature_status=O
|Other_designations=ALL1-related protein;;Kabuki make-up syndrome;;Kabuki mental retardation syndrome;;histone-lysine N-methyltransferase MLL2;;lysine N-methyltransferase 2B;;lysine N-methyltransferase 2D;;trinucleotide repeat containing 21
|Symbol=MLL2
|Symbol=MLL2
|LocusTag=-
|Symbol_from_nomenclature_authority=MLL2
|Synonyms=AAD10;;ALR;;CAGL114;;KMS;;KMT2B;;KMT2D;;MLL4;;TNRC21
|Synonyms=AAD10;;ALR;;CAGL114;;KMS;;KMT2B;;KMT2D;;MLL4;;TNRC21
|dbXrefs=HGNC:7133;;MIM:602113;;Ensembl:ENSG00000167548;;HPRD:03664;;Vega:OTTHUMG00000166524
|chromosome=12
|chromosome=12
|dbXrefs=HGNC:7133;;MIM:602113;;Ensembl:ENSG00000167548;;HPRD:03664;;Vega:OTTHUMG00000166524;;EpiFactors:8085:genes
|description=myeloid/lymphoid or mixed-lineage leukemia 2
|map_location=12q13.12
|map_location=12q13.12
|description=myeloid/lymphoid or mixed-lineage leukemia 2
|tax_id=9606
|tf?=yes
|transcription_factor=
|type_of_gene=protein-coding
|type_of_gene=protein-coding
|Symbol_from_nomenclature_authority=MLL2
|Full_name_from_nomenclature_authority=myeloid/lymphoid or mixed-lineage leukemia 2
|Nomenclature_status=O
|Other_designations=ALL1-related protein;;Kabuki make-up syndrome;;Kabuki mental retardation syndrome;;histone-lysine N-methyltransferase MLL2;;lysine N-methyltransferase 2B;;lysine N-methyltransferase 2D;;trinucleotide repeat containing 21
|Modification_date=20120108
|transcription_factor=
}}
}}

Latest revision as of 13:24, 26 June 2015

Symbol:MLL2
Description:myeloid/lymphoid or mixed-lineage leukemia 2
Synonyms:AAD10, ALR, CAGL114, KMS, KMT2B, KMT2D, MLL4, TNRC21
Species:Human (Homo sapiens)
Xrefs:
EntrezGene:8085
HGNC:7133
MIM:602113
Ensembl:ENSG00000167548
HPRD:03664
Vega:OTTHUMG00000166524
EpiFactors:8085
Associated motifs:NA
Transcripton Factor?: Yes

TSS regions




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TSS expression






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  • Click each plot point to find sample in table

ENCODE TF ChIP-seq peak enrichment analysis Analyst: Erik Arner <br>Summary: For each TF and each co-expression cluster, the number of promoters with ENCODE TF ChIP signal was compared with the rest of promoters from the robust set using Fisher's exact test. Clusters with significant ChIP enrichment (q <= 0.05) after Benjamini-Hochberg correction were retained. <br><br><br>link to source dataset.<br>data


No analysis results for this cluster

Details<b>Summary:</b>It includes sequences from the international sequence collaboration, Swiss-Prot, and RefSeq. The RefSeq subset of this file is also available as gene2refseq.<br><br>links to source dataset.<br>human <br>mouse


GeneID:8085
LocusTag:-
chromosome:12
map location:12q13.12
type of gene:protein-coding
Symbol from
nomenclature authority:
MLL2
Full name from
nomenclature authority:
myeloid/lymphoid or mixed-lineage leukemia 2
Nomenclature status:O
Other designations:ALL1-related protein, Kabuki make-up syndrome, Kabuki mental retardation syndrome, histone-lysine N-methyltransferase MLL2, lysine N-methyltransferase 2B, lysine N-methyltransferase 2D, trinucleotide repeat containing 21, ALL1-related protein;;Kabuki make-up syndrome;;Kabuki mental retardation syndrome;;histone-lysine N-methyltransferase MLL2;;lysine N-methyltransferase 2B;;lysine N-methyltransferase 2D;;trinucleotide repeat containing 21
Modification date:08.01.2012