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Gene : LOC109648316 Homo sapiens

Name  ? RUNX1 element RE2
description  This record represents a conserved sequence located in the fifth intron of the runt related transcription factor 1 (RUNX1) gene. This sequence was shown to have physical interactions with the RUNX1 P1 and P2 promoters and may be important for RUNX1 transcription. Naturally occurring polymorphisms in this region are associated with acute myeloid leukemia and may influence the ability of this sequence to function as an enhancer. [provided by RefSeq, Feb 2017]
  • identifiers:
  • 109648316,
  • LOC109648316

Genome feature

Region: gene ?
Location: No location information in HumanMine

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0 Pathways

Gene --> GO terms.

Gene -> HPO annotation (Human Phenotype Ontology)

Mouse Gene --> Allele [Phenotype]


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Gene --> Chromosomal location.

Gene --> GO terms.

Gene --> Overlapping genes.


Gene --> Proteins.


Gene Report --> GWAS hit


0 Diseases

Gene (Hum OR Rat) --> Mouse Allele (Phenotype)

Gene --> Alleles and Disease (clinVar data)

Gene -> HPO annotation (Human Phenotype Ontology)

Mouse Gene --> Allele [Phenotype]


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Gene --> Orthologues


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Gene --> Physical and Genetic Interactions


Gene(s) --> Significant SNPs (GTex data)

Gene Ontology

Gene --> GO terms.



0 Pathways

0 SN Ps

1 Cross References

3 Data Sets

0 Homologues

0 Located Features

0 Rna Seq Results