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Gene : SLX4 Homo sapiens

Name  ? SLX4 structure-specific endonuclease subunit Cytological Location  16p13.3
Brief Description  SLX4 structure-specific endonuclease subunit
Description  This gene encodes a protein that functions as an assembly component of multiple structure-specific endonucleases. These endonuclease complexes are required for repair of specific types of DNA lesions and critical for cellular responses to replication fork failure. Mutations in this gene were found in patients with Fanconi anemia. [provided by RefSeq, Sep 2016]
  • synonyms:
  • KIAA1784,
  • SLX4 structure-specific endonuclease subunit homolog (S. cerevisiae),
  • MUS312,
  • FANCP,
  • FANCP,
  • SLX4,
  • NM_032444,
  • uc002cvp.3,
  • BTBD12,
  • Fanconi anemia, complementation group P,
  • AB058687,
  • BTBD12,
  • HGNC:23845,
  • KIAA1987,
  • BTB (POZ) domain containing 12,
  • OTTHUMG00000074089
  • identifiers:
  • 84464,
  • ENSG00000188827,
  • SLX4

Genome feature

Region: gene ? Length: 31987  
Location: 16:3579653-3611639 reverse strand Cyto location: 16p13.3


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Proteins

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SNPs

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Disease

1 Diseases

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

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Gene -> HPO annotation (Human Phenotype Ontology)

Mouse Gene --> Allele [Phenotype]

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Expression

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Other

258 SN Ps

5 Cross References

18 Data Sets

5 Homologues

0 Located Features

97 Rna Seq Results