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Gene : LOC107522031 Homo sapiens

Name  ? meiotic recombination hotspot CG Cytological Location  16p13.3
description  This region is located within an intron of the RNA binding protein, fox-1 homolog (C. elegans) 1 (RBFOX1) gene on the p arm of chromosome 16, and has been identified as a meiotic recombination hotspot by sperm typing assays, molecular assays in male germ cells to identify meiotic double strand breaks, and linkage disequilibrium studies. This meiotic recombination hotspot tends to have a higher recombination frequency in individuals bearing either a PRDM9 A or B allele, with little to no meiotic recombination activity observed in some individuals with other PRDM9 alleles. Meiotic hotspot activity can vary widely amongst individuals and can be influenced by both the nucleotide sequence at the meiotic recombination hotspot and the specific alleles present at the PR domain 9 (PRDM9) locus. [provided by RefSeq, Apr 2016]
  • identifiers:
  • 107522031,
  • LOC107522031

Genome feature

Region: gene ?
Location: No location information in HumanMine Cyto location: 16p13.3

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0 Pathways

Gene --> GO terms.

Mouse Gene --> Allele [Phenotype]


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Gene --> Chromosomal location.

Gene --> GO terms.

Gene --> Overlapping genes.


Gene --> Proteins.


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0 Diseases

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

Gene --> Alleles and Disease (clinVar data)

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