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Gene : LOC108903149 Homo sapiens

Name  ? 10p13 OPTN proximal Alu-mediated recombination region Cytological Location  10p13
description  This biological region is known to undergo Alu-repeat-mediated non-allelic homologous recombination (NAHR) with the 10p13 OPTN distal Alu-mediated recombination region, located just centromere-distal of this region, in direct orientation. NAHR events between these regions can lead to deletions of the intervening sequence, and such deletions are thought to be associated with amyotrophic lateral sclerosis (ALS). NAHR sub-regions are found within Alu repeat elements, and the repetitive nature of these elements may play an important role in providing substrates for recombination. [provided by RefSeq, Oct 2016]
  • identifiers:
  • 108903149,
  • LOC108903149

Genome feature

Region: gene ?
Location: No location information in HumanMine Cyto location: 10p13

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0 Pathways

Gene --> GO terms.

Gene -> HPO annotation (Human Phenotype Ontology)

Mouse Gene --> Allele [Phenotype]


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Gene --> Proteins.


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

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Gene --> GO terms.



0 Pathways

0 SN Ps

1 Cross References

3 Data Sets

0 Homologues

0 Located Features

0 Rna Seq Results