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GENE - TERM ANNOTATION REPORT

2 Annotations Found.

An association has been curated linking SLX4 and Fanconi anemia complementation group P in Sus scrofa.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from OMIM Disease Annotation Pipeline
  • The annotation has been inferred from sequence orthology with SLX4 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Fanconi anemia complementation group P  (DOID:0111092)
  • 0 papers in RGD have been used to annotate SLX4


  • An association has been curated linking SLX4 and Fanconi anemia complementation group P in Sus scrofa.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with SLX4 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Fanconi anemia complementation group P  (DOID:0111092)
  • 0 papers in RGD have been used to annotate SLX4
  • Curation Notes: ClinVar Annotator: match by term: Fanconi anemia complementation group P
  • Original References(s): PMID:17576681 PMID:21240275 PMID:21240277 PMID:21805310 PMID:22383991 PMID:22401137 PMID:22911665 PMID:23211700 PMID:23840564 PMID:23994477 PMID:24763404 PMID:25288723 PMID:25326635 PMID:25741868 PMID:26201965 PMID:26824983 PMID:27153395 PMID:28125078 PMID:28202063 PMID:28492532 PMID:28678401 PMID:29146900 PMID:29344583 PMID:29607586 PMID:29641532 PMID:29868112 PMID:29891941 PMID:30268473 PMID:30306255 PMID:30613976 PMID:30995915 PMID:31300551 PMID:31469826 PMID:32368696 PMID:32546565 PMID:33270637 PMID:33558524 PMID:36916425 PMID:9536098


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