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Gene : 109623491 Homo sapiens

Description  This biological region is found on the p arm of chromosome 7, and contains a highly variable minisatellite region with tandem repeats of about 20 nucleotides in length. Repeats typically contain the sequence CCACCTCCCACAGACACT(GC/GT). Repeat instability due to unequal crossing over between alleles and gene conversion during meiosis has been observed in this region. There is also another minisatellite region, MS31B, in close proximity to this region. This region contains a meiotic recombination hotspot that partially overlaps the variable number tandem repeat. [provided by RefSeq, Feb 2017]
  • identifiers:
  • 109623491

Genome feature

Region: gene ?
Location: No location information in HumanMine


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Function

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0 Pathways

Gene --> GO terms.

Gene -> HPO annotation (Human Phenotype Ontology)

Mouse Gene --> Allele [Phenotype]

Genomics

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Gene --> Chromosomal location.

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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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Expression

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

Gene Ontology

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Other

0 Pathways

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1 Data Sets

0 Homologues

0 Located Features

0 Rna Seq Results