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Gene : 108169207 Homo sapiens

Description  This genomic region is located on chromosome 6 in the intergenic interval between the OLIG3 (oligodendrocyte transcription factor 3) and TNFAIP3 (TNF alpha induced protein 3) genes. It was identified as a homotypic cluster of transcription factor binding sites (HCT) based on the presence of multiple binding motifs for POU3F2 (POU class 3 homeobox 2). This HCT was validated as a functional enhancer in transgenic reporter assays in zebrafish. [provided by RefSeq, Jun 2016]
  • identifiers:
  • 108169207

Genome feature

Region: gene ?
Location: No location information in HumanMine


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Function

Gene Ontology Displayer

0 Pathways

Gene --> GO terms.

Gene -> HPO annotation (Human Phenotype Ontology)

Mouse Gene --> Allele [Phenotype]

Genomics

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Gene --> Chromosomal location.

Gene --> GO terms.

Gene --> Overlapping genes.

Proteins

Gene --> Proteins.

SNPs

Gene Report --> GWAS hit

Disease

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]

Homology

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Interactions

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Gene --> Physical and Genetic Interactions

Expression

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

Gene Ontology

Gene --> GO terms.

 

Other

0 Pathways

0 SN Ps

0 Cross References

1 Data Sets

0 Homologues

0 Located Features

0 Rna Seq Results