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GENE - TERM ANNOTATION REPORT

108 Annotations Found.

An association has been curated linking PALB2 and Fanconi anemia complementation group N in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • 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 by association of genotype and phenotype with RGD:8658569 (Homo sapiens)
  • 1 RGD objects have been annotated to Fanconi anemia complementation group N  (DOID:0111094)
  • 8 papers in RGD have been used to annotate PALB2
  • Curation Notes: ClinVar Annotator: match by term: Fanconi anemia complementation group N
  • Original References(s): PMID:17200668 PMID:17200671 PMID:19264984 PMID:19584259 PMID:19609323 PMID:20927582 PMID:21165770 PMID:21365267 PMID:25099575 PMID:25741868 PMID:26283626 PMID:26296701 PMID:26315354 PMID:26467025 PMID:26641009 PMID:26681312 PMID:28492532 PMID:29360161 PMID:31159747 PMID:31757951 PMID:32339256


    • An association has been curated linking PALB2 and Fanconi anemia complementation group N in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • 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 by association of genotype and phenotype with RGD:9834655 (Homo sapiens)
  • 1 RGD objects have been annotated to Fanconi anemia complementation group N  (DOID:0111094)
  • 8 papers in RGD have been used to annotate PALB2
  • Curation Notes: ClinVar Annotator: match by term: Fanconi anemia complementation group N
  • Original References(s): PMID:25085752 PMID:25741868 PMID:28492532


    • An association has been curated linking PALB2 and Fanconi anemia complementation group N in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • 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 by association of genotype and phenotype with RGD:26887836 (Homo sapiens)
  • 1 RGD objects have been annotated to Fanconi anemia complementation group N  (DOID:0111094)
  • 8 papers in RGD have been used to annotate PALB2
  • Curation Notes: ClinVar Annotator: match by term: Fanconi anemia complementation group N
  • Original References(s): PMID:17200672


    • An association has been curated linking PALB2 and Fanconi anemia complementation group N in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • 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 by association of genotype and phenotype with RGD:26887817 (Homo sapiens)
  • 1 RGD objects have been annotated to Fanconi anemia complementation group N  (DOID:0111094)
  • 8 papers in RGD have been used to annotate PALB2
  • Curation Notes: ClinVar Annotator: match by term: Fanconi anemia complementation group N
  • Original References(s): PMID:17924555


    • An association has been curated linking PALB2 and Fanconi anemia complementation group N in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • 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 by association of genotype and phenotype with RGD:12899973 (Homo sapiens)
  • 1 RGD objects have been annotated to Fanconi anemia complementation group N  (DOID:0111094)
  • 8 papers in RGD have been used to annotate PALB2
  • Curation Notes: ClinVar Annotator: match by term: Fanconi anemia complementation group N
  • Original References(s): PMID:25356972 PMID:25741868 PMID:28492532 PMID:28726808 PMID:30638972


    • An association has been curated linking PALB2 and Fanconi anemia complementation group N in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • 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 by association of genotype and phenotype with RGD:8591318 (Homo sapiens)
  • 1 RGD objects have been annotated to Fanconi anemia complementation group N  (DOID:0111094)
  • 8 papers in RGD have been used to annotate PALB2
  • Curation Notes: ClinVar Annotator: match by term: Fanconi anemia complementation group N
  • Original References(s): PMID:17200668 PMID:17287723 PMID:17420451 PMID:18288683 PMID:18302019 PMID:20927582 PMID:21356067 PMID:21365267 PMID:21409391 PMID:21618343 PMID:21932393 PMID:22052327 PMID:22241545 PMID:22310028 PMID:22692731 PMID:23448497 PMID:23824750 PMID:23935836 PMID:24206657 PMID:24556926 PMID:24728327 PMID:24949998 PMID:25741868 PMID:26283626 PMID:28492532


    • An association has been curated linking PALB2 and Fanconi anemia complementation group N in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • 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 by association of genotype and phenotype with RGD:8591314 (Homo sapiens)
  • 1 RGD objects have been annotated to Fanconi anemia complementation group N  (DOID:0111094)
  • 8 papers in RGD have been used to annotate PALB2
  • Curation Notes: ClinVar Annotator: match by term: Fanconi anemia complementation group N
  • Original References(s): PMID:18302019 PMID:18446436 PMID:20180015 PMID:20852946 PMID:21618343 PMID:22052327 PMID:22310028 PMID:22692731 PMID:23448497 PMID:23824750 PMID:23935836 PMID:24556926 PMID:25741868


    • An association has been curated linking PALB2 and Fanconi anemia complementation group N in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • 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 by association of genotype and phenotype with RGD:8591316 (Homo sapiens)
  • 1 RGD objects have been annotated to Fanconi anemia complementation group N  (DOID:0111094)
  • 8 papers in RGD have been used to annotate PALB2
  • Curation Notes: ClinVar Annotator: match by term: Fanconi anemia complementation group N
  • Original References(s): PMID:21356067 PMID:25356972 PMID:25741868 PMID:28492532


    • An association has been curated linking PALB2 and Fanconi anemia complementation group N in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • 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 by association of genotype and phenotype with RGD:8591340 (Homo sapiens)
  • 1 RGD objects have been annotated to Fanconi anemia complementation group N  (DOID:0111094)
  • 8 papers in RGD have been used to annotate PALB2
  • Curation Notes: ClinVar Annotator: match by term: Fanconi anemia complementation group N
  • Original References(s): PMID:17200668 PMID:20582465 PMID:21165770 PMID:23448497 PMID:24206657 PMID:25225577 PMID:25741868 PMID:26283626 PMID:26467025 PMID:26564480 PMID:28492532


    • An association has been curated linking PALB2 and Fanconi anemia complementation group N in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • 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 by association of genotype and phenotype with RGD:8591493 (Homo sapiens)
  • 1 RGD objects have been annotated to Fanconi anemia complementation group N  (DOID:0111094)
  • 8 papers in RGD have been used to annotate PALB2
  • Curation Notes: ClinVar Annotator: match by term: Fanconi anemia complementation group N
  • Original References(s): PMID:18288683 PMID:21113654 PMID:21165770 PMID:21932393 PMID:24728327 PMID:25741868 PMID:26283626 PMID:28492532


    • An association has been curated linking PALB2 and Fanconi anemia complementation group N in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • 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 by association of genotype and phenotype with RGD:8591513 (Homo sapiens)
  • 1 RGD objects have been annotated to Fanconi anemia complementation group N  (DOID:0111094)
  • 8 papers in RGD have been used to annotate PALB2
  • Curation Notes: ClinVar Annotator: match by term: Fanconi anemia complementation group N
  • Original References(s): PMID:18288683 PMID:21932393 PMID:25741868 PMID:28492532


    • An association has been curated linking PALB2 and Fanconi anemia complementation group N in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • 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 by association of genotype and phenotype with RGD:8591515 (Homo sapiens)
  • 1 RGD objects have been annotated to Fanconi anemia complementation group N  (DOID:0111094)
  • 8 papers in RGD have been used to annotate PALB2
  • Curation Notes: ClinVar Annotator: match by term: Fanconi anemia complementation group N
  • Original References(s): PMID:17200668 PMID:18288683 PMID:19333784 PMID:21113654 PMID:21932393 PMID:23824750 PMID:23977390 PMID:24728327 PMID:25741868 PMID:26283626 PMID:28492532 PMID:30287823


    • An association has been curated linking PALB2 and Fanconi anemia complementation group N in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • 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 by association of genotype and phenotype with RGD:8591511 (Homo sapiens)
  • 1 RGD objects have been annotated to Fanconi anemia complementation group N  (DOID:0111094)
  • 8 papers in RGD have been used to annotate PALB2
  • Curation Notes: ClinVar Annotator: match by term: Fanconi anemia complementation group N
  • Original References(s): PMID:19763884 PMID:25741868 PMID:26467025 PMID:28492532


    • An association has been curated linking PALB2 and Fanconi anemia complementation group N in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • 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 by association of genotype and phenotype with RGD:8591349 (Homo sapiens)
  • 1 RGD objects have been annotated to Fanconi anemia complementation group N  (DOID:0111094)
  • 8 papers in RGD have been used to annotate PALB2
  • Curation Notes: ClinVar Annotator: match by term: Fanconi anemia complementation group N
  • Original References(s): PMID:17200668 PMID:17200672 PMID:17287723 PMID:18288683 PMID:18302019 PMID:18446436 PMID:19333784 PMID:19763884 PMID:20180015 PMID:20927582 PMID:21113654 PMID:21165770 PMID:21356067 PMID:21365267 PMID:21409391 PMID:21618343 PMID:21932393 PMID:22052327 PMID:22241545 PMID:22310028 PMID:23448497 PMID:23824750 PMID:23935836 PMID:23977390 PMID:24206657 PMID:24556926 PMID:24728327 PMID:24949998 PMID:25741868 PMID:26283626 PMID:28492532 PMID:30287823


    • An association has been curated linking PALB2 and Fanconi anemia complementation group N in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • 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 by association of genotype and phenotype with RGD:8591465 (Homo sapiens)
  • 1 RGD objects have been annotated to Fanconi anemia complementation group N  (DOID:0111094)
  • 8 papers in RGD have been used to annotate PALB2
  • Curation Notes: ClinVar Annotator: match by term: Fanconi anemia complementation group N
  • Original References(s): PMID:17200668 PMID:17287723 PMID:18288683 PMID:18302019 PMID:19333784 PMID:20122277 PMID:20852946 PMID:20927582 PMID:21165770 PMID:21365267 PMID:21409391 PMID:21618343 PMID:22052327 PMID:22310028 PMID:22692731 PMID:23448497 PMID:23935836 PMID:24206657 PMID:24556926 PMID:24949998 PMID:25741868 PMID:26283626 PMID:28492532


    • An association has been curated linking PALB2 and Fanconi anemia complementation group N in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • 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 by association of genotype and phenotype with RGD:8591307 (Homo sapiens)
  • 1 RGD objects have been annotated to Fanconi anemia complementation group N  (DOID:0111094)
  • 8 papers in RGD have been used to annotate PALB2
  • Curation Notes: ClinVar Annotator: match by term: Fanconi anemia complementation group N
  • Original References(s): PMID:21285249 PMID:21618343 PMID:22052327 PMID:23824750


    • An association has been curated linking PALB2 and Fanconi anemia complementation group N in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • 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 by association of genotype and phenotype with RGD:8591496 (Homo sapiens)
  • 1 RGD objects have been annotated to Fanconi anemia complementation group N  (DOID:0111094)
  • 8 papers in RGD have been used to annotate PALB2
  • Curation Notes: ClinVar Annotator: match by term: Fanconi anemia complementation group N
  • Original References(s): PMID:17200668 PMID:18302019 PMID:21113654 PMID:21932393 PMID:22241545 PMID:24728327 PMID:25741868 PMID:26283626 PMID:28492532


    • An association has been curated linking PALB2 and Fanconi anemia complementation group N in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • 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 by association of genotype and phenotype with RGD:8591303 (Homo sapiens)
  • 1 RGD objects have been annotated to Fanconi anemia complementation group N  (DOID:0111094)
  • 8 papers in RGD have been used to annotate PALB2
  • Curation Notes: ClinVar Annotator: match by term: Fanconi anemia complementation group N
  • Original References(s): PMID:21932393


    • An association has been curated linking PALB2 and Fanconi anemia complementation group N in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • 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 by association of genotype and phenotype with RGD:8591366 (Homo sapiens)
  • 1 RGD objects have been annotated to Fanconi anemia complementation group N  (DOID:0111094)
  • 8 papers in RGD have been used to annotate PALB2
  • Curation Notes: ClinVar Annotator: match by term: Fanconi anemia complementation group N
  • Original References(s): PMID:17200668 PMID:18288683 PMID:18302019 PMID:19333784 PMID:20122277 PMID:20180015 PMID:20927582 PMID:21165770 PMID:21365267 PMID:21409391 PMID:21618343 PMID:21932393 PMID:22052327 PMID:22241545 PMID:22310028 PMID:22692731 PMID:23448497 PMID:23824750 PMID:23935836 PMID:24033266 PMID:24206657 PMID:24556926 PMID:24728327 PMID:24949998 PMID:25741868 PMID:26283626 PMID:28492532


    • An association has been curated linking PALB2 and Fanconi anemia complementation group N in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • 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 by association of genotype and phenotype with RGD:8692309 (Homo sapiens)
  • 1 RGD objects have been annotated to Fanconi anemia complementation group N  (DOID:0111094)
  • 8 papers in RGD have been used to annotate PALB2
  • Curation Notes: ClinVar Annotator: match by term: Fanconi anemia complementation group N
  • Original References(s): PMID:25741868 PMID:26283626 PMID:26467025 PMID:28492532 PMID:28779002


    • An association has been curated linking PALB2 and Fanconi anemia complementation group N in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • 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 by association of genotype and phenotype with RGD:8689913 (Homo sapiens)
  • 1 RGD objects have been annotated to Fanconi anemia complementation group N  (DOID:0111094)
  • 8 papers in RGD have been used to annotate PALB2
  • Curation Notes: ClinVar Annotator: match by term: Fanconi anemia complementation group N
  • Original References(s): PMID:25741868 PMID:26283626 PMID:28492532


    • An association has been curated linking PALB2 and Fanconi anemia complementation group N in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • 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 by association of genotype and phenotype with RGD:11090490 (Homo sapiens)
  • 1 RGD objects have been annotated to Fanconi anemia complementation group N  (DOID:0111094)
  • 8 papers in RGD have been used to annotate PALB2
  • Curation Notes: ClinVar Annotator: match by term: Fanconi anemia complementation group N
  • Original References(s): PMID:26990772


    • An association has been curated linking PALB2 and Fanconi anemia complementation group N in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • 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 by association of genotype and phenotype with RGD:8591417 (Homo sapiens)
  • 1 RGD objects have been annotated to Fanconi anemia complementation group N  (DOID:0111094)
  • 8 papers in RGD have been used to annotate PALB2
  • Curation Notes: ClinVar Annotator: match by term: Fanconi anemia complementation group N
  • Original References(s): PMID:17200668 PMID:17287723 PMID:18302019 PMID:20927582 PMID:21165770 PMID:21356067 PMID:21365267 PMID:21409391 PMID:22241545 PMID:22310028 PMID:24448499 PMID:24556926 PMID:24728327 PMID:24949998 PMID:25356972 PMID:25479140 PMID:25741868 PMID:26283626 PMID:28492532


    • An association has been curated linking PALB2 and Fanconi anemia complementation group N in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • 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 by association of genotype and phenotype with RGD:9834681 (Homo sapiens)
  • 1 RGD objects have been annotated to Fanconi anemia complementation group N  (DOID:0111094)
  • 8 papers in RGD have been used to annotate PALB2
  • Curation Notes: ClinVar Annotator: match by term: Fanconi anemia complementation group N
  • Original References(s): PMID:25741868 PMID:26283626 PMID:26315354 PMID:28492532


    • An association has been curated linking PALB2 and Fanconi anemia complementation group N in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • 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 by association of genotype and phenotype with RGD:8697138 (Homo sapiens)
  • 1 RGD objects have been annotated to Fanconi anemia complementation group N  (DOID:0111094)
  • 8 papers in RGD have been used to annotate PALB2
  • Curation Notes: ClinVar Annotator: match by term: Fanconi anemia complementation group N
  • Original References(s): PMID:25741868 PMID:28492532 PMID:30287823 PMID:32566746


    • An association has been curated linking PALB2 and Fanconi anemia complementation group N in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • 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 by association of genotype and phenotype with RGD:8591431 (Homo sapiens)
  • 1 RGD objects have been annotated to Fanconi anemia complementation group N  (DOID:0111094)
  • 8 papers in RGD have been used to annotate PALB2
  • Curation Notes: ClinVar Annotator: match by term: Fanconi anemia complementation group N
  • Original References(s): PMID:17200668 PMID:17200671 PMID:17200672 PMID:17420451 PMID:21285249 PMID:24136930 PMID:24870022 PMID:25099575 PMID:25741868 PMID:26681312 PMID:26898890 PMID:28492532 PMID:28779002


    • An association has been curated linking PALB2 and Fanconi anemia complementation group N in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • 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 by association of genotype and phenotype with RGD:8698018 (Homo sapiens)
  • 1 RGD objects have been annotated to Fanconi anemia complementation group N  (DOID:0111094)
  • 8 papers in RGD have been used to annotate PALB2
  • Curation Notes: ClinVar Annotator: match by term: Fanconi anemia complementation group N
  • Original References(s): PMID:17200668 PMID:17200671 PMID:17200672 PMID:24136930 PMID:25099575 PMID:25741868 PMID:26467025 PMID:26681312 PMID:27433846 PMID:28492532


    • An association has been curated linking PALB2 and Fanconi anemia complementation group N in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • 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 by association of genotype and phenotype with RGD:9834680 (Homo sapiens)
  • 1 RGD objects have been annotated to Fanconi anemia complementation group N  (DOID:0111094)
  • 8 papers in RGD have been used to annotate PALB2
  • Curation Notes: ClinVar Annotator: match by term: Fanconi anemia complementation group N
  • Original References(s): PMID:23977390 PMID:25186627 PMID:25741868 PMID:26283626 PMID:26411315 PMID:26467025 PMID:26692951 PMID:27783279 PMID:28492532 PMID:28580595 PMID:28767289 PMID:28825143 PMID:30287823 PMID:32566746


    • An association has been curated linking PALB2 and Fanconi anemia complementation group N in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • 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 by association of genotype and phenotype with RGD:9853956 (Homo sapiens)
  • 1 RGD objects have been annotated to Fanconi anemia complementation group N  (DOID:0111094)
  • 8 papers in RGD have been used to annotate PALB2
  • Curation Notes: ClinVar Annotator: match by term: Fanconi anemia complementation group N
  • Original References(s): PMID:17200668 PMID:17200671 PMID:17200672 PMID:24136930 PMID:25099575 PMID:25741868 PMID:26485759 PMID:28492532


    • An association has been curated linking PALB2 and Fanconi anemia complementation group N in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • 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 by association of genotype and phenotype with RGD:8591344 (Homo sapiens)
  • 1 RGD objects have been annotated to Fanconi anemia complementation group N  (DOID:0111094)
  • 8 papers in RGD have been used to annotate PALB2
  • Curation Notes: ClinVar Annotator: match by term: Fanconi anemia complementation group N
  • Original References(s): PMID:17200668 PMID:18288683 PMID:18302019 PMID:19635604 PMID:20582465 PMID:20927582 PMID:21165770 PMID:21365267 PMID:21618343 PMID:22052327 PMID:23448497 PMID:23935836 PMID:24206657 PMID:24556926 PMID:24949998 PMID:25447460 PMID:25741868 PMID:26283626 PMID:26467025 PMID:27067391 PMID:28492532 PMID:30521987


    • An association has been curated linking PALB2 and Fanconi anemia complementation group N in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • 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 by association of genotype and phenotype with RGD:9852956 (Homo sapiens)
  • 1 RGD objects have been annotated to Fanconi anemia complementation group N  (DOID:0111094)
  • 8 papers in RGD have been used to annotate PALB2
  • Curation Notes: ClinVar Annotator: match by term: Fanconi anemia complementation group N
  • Original References(s): PMID:25741868 PMID:26467025 PMID:28492532 PMID:30287823


    • An association has been curated linking PALB2 and Fanconi anemia complementation group N in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • 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 by association of genotype and phenotype with RGD:8591328 (Homo sapiens)
  • 1 RGD objects have been annotated to Fanconi anemia complementation group N  (DOID:0111094)
  • 8 papers in RGD have been used to annotate PALB2
  • Curation Notes: ClinVar Annotator: match by term: Fanconi anemia complementation group N
  • Original References(s): PMID:17200668 PMID:18302019 PMID:21365267 PMID:21618343 PMID:22052327 PMID:23935836 PMID:24556926 PMID:24949998 PMID:25741868 PMID:26283626 PMID:26467025 PMID:26564480 PMID:27573125 PMID:28492532 PMID:29052111 PMID:33512806


    • An association has been curated linking PALB2 and Fanconi anemia complementation group N in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • 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 by association of genotype and phenotype with RGD:8591443 (Homo sapiens)
  • 1 RGD objects have been annotated to Fanconi anemia complementation group N  (DOID:0111094)
  • 8 papers in RGD have been used to annotate PALB2
  • Curation Notes: ClinVar Annotator: match by term: Fanconi anemia complementation group N
  • Original References(s): PMID:21285249 PMID:22241545 PMID:23977390 PMID:25575445 PMID:25741868 PMID:26283626 PMID:26411315 PMID:26467025 PMID:26489409 PMID:26692951 PMID:27616075 PMID:27783279 PMID:28492532 PMID:28580595 PMID:28664506 PMID:28825143 PMID:30287823 PMID:31159747 PMID:31757951 PMID:32531196 PMID:32566746 PMID:33471991


    • An association has been curated linking PALB2 and Fanconi anemia complementation group N in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • 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 by association of genotype and phenotype with RGD:8591396 (Homo sapiens)
  • 1 RGD objects have been annotated to Fanconi anemia complementation group N  (DOID:0111094)
  • 8 papers in RGD have been used to annotate PALB2
  • Curation Notes: ClinVar Annotator: match by term: Fanconi anemia complementation group N
  • Original References(s): PMID:21285249 PMID:25085752 PMID:25356972 PMID:25741868 PMID:26467025 PMID:28492532


    • An association has been curated linking PALB2 and Fanconi anemia complementation group N in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from OMIM Disease Annotation Pipeline
  • 1 RGD objects have been annotated to Fanconi anemia complementation group N  (DOID:0111094)
  • 8 papers in RGD have been used to annotate PALB2
  • Qualifier: susceptibility


    • An association has been curated linking PALB2 and Fanconi anemia complementation group N in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • 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 by association of genotype and phenotype with RGD:151759610 (Homo sapiens)
  • 1 RGD objects have been annotated to Fanconi anemia complementation group N  (DOID:0111094)
  • 8 papers in RGD have been used to annotate PALB2
  • Curation Notes: ClinVar Annotator: match by term: Fanconi anemia complementation group N
  • Original References(s): PMID:17200668 PMID:17200671 PMID:17200672 PMID:24136930 PMID:25099575 PMID:25741868 PMID:28492532


    • An association has been curated linking PALB2 and Fanconi anemia complementation group N in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • 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 by association of genotype and phenotype with RGD:13512103 (Homo sapiens)
  • 1 RGD objects have been annotated to Fanconi anemia complementation group N  (DOID:0111094)
  • 8 papers in RGD have been used to annotate PALB2
  • Curation Notes: ClinVar Annotator: match by term: Fanconi anemia complementation group N
  • Original References(s): PMID:25741868 PMID:26467025 PMID:29470806


    • An association has been curated linking PALB2 and Fanconi anemia complementation group N in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • 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 by association of genotype and phenotype with RGD:12858922 (Homo sapiens)
  • 1 RGD objects have been annotated to Fanconi anemia complementation group N  (DOID:0111094)
  • 8 papers in RGD have been used to annotate PALB2
  • Curation Notes: ClinVar Annotator: match by term: Fanconi anemia complementation group N
  • Original References(s): PMID:17200668 PMID:17200671 PMID:17200672 PMID:24136930 PMID:25099575 PMID:25741868 PMID:28492532 PMID:30287823


    • An association has been curated linking PALB2 and Fanconi anemia complementation group N in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • 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 by association of genotype and phenotype with RGD:13509827 (Homo sapiens)
  • 1 RGD objects have been annotated to Fanconi anemia complementation group N  (DOID:0111094)
  • 8 papers in RGD have been used to annotate PALB2
  • Curation Notes: ClinVar Annotator: match by term: Fanconi anemia complementation group N
  • Original References(s): PMID:21618343 PMID:25741868 PMID:27616075 PMID:28492532


    • An association has been curated linking PALB2 and Fanconi anemia complementation group N in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • 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 by association of genotype and phenotype with RGD:8689917 (Homo sapiens)
  • 1 RGD objects have been annotated to Fanconi anemia complementation group N  (DOID:0111094)
  • 8 papers in RGD have been used to annotate PALB2
  • Curation Notes: ClinVar Annotator: match by term: Fanconi anemia complementation group N
  • Original References(s): PMID:17200668 PMID:17200671 PMID:17200672 PMID:24033266 PMID:24136930 PMID:24448499 PMID:24556926 PMID:25099575 PMID:25741868 PMID:26315354 PMID:26467025 PMID:26845104 PMID:27624329 PMID:28492532 PMID:28724667 PMID:29752822 PMID:29945567 PMID:30322717 PMID:31206626 PMID:31263054 PMID:31447099 PMID:31844177 PMID:32339256 PMID:32566746 PMID:36988593


    • An association has been curated linking PALB2 and Fanconi anemia complementation group N in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • 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 by association of genotype and phenotype with RGD:8658558 (Homo sapiens)
  • 1 RGD objects have been annotated to Fanconi anemia complementation group N  (DOID:0111094)
  • 8 papers in RGD have been used to annotate PALB2
  • Curation Notes: ClinVar Annotator: match by term: Fanconi anemia complementation group N
  • Original References(s): PMID:24728327 PMID:25741868 PMID:26411315 PMID:26467025 PMID:27783279 PMID:28380452 PMID:28492532 PMID:28796317 PMID:29190888 PMID:30287823 PMID:32019277 PMID:32566746 PMID:33309985 PMID:33471991


    • An association has been curated linking PALB2 and Fanconi anemia complementation group N in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • 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 by association of genotype and phenotype with RGD:8698114 (Homo sapiens)
  • 1 RGD objects have been annotated to Fanconi anemia complementation group N  (DOID:0111094)
  • 8 papers in RGD have been used to annotate PALB2
  • Curation Notes: ClinVar Annotator: match by term: Fanconi anemia complementation group N
  • Original References(s): PMID:25085752 PMID:25186627 PMID:25741868 PMID:26315354 PMID:26467025 PMID:26976419 PMID:28492532 PMID:28779002 PMID:30883245 PMID:31159747 PMID:31422574 PMID:31428572 PMID:31636395 PMID:33471991 PMID:35402282 PMID:35610400


    • An association has been curated linking PALB2 and Fanconi anemia complementation group N in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • 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 by association of genotype and phenotype with RGD:12880996 (Homo sapiens)
  • 1 RGD objects have been annotated to Fanconi anemia complementation group N  (DOID:0111094)
  • 8 papers in RGD have been used to annotate PALB2
  • Curation Notes: ClinVar Annotator: match by term: Fanconi anemia complementation group N
  • Original References(s): PMID:17200668 PMID:25099575 PMID:25741868 PMID:28492532


    • An association has been curated linking PALB2 and Fanconi anemia complementation group N in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • 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 by association of genotype and phenotype with RGD:8591480 (Homo sapiens)
  • 1 RGD objects have been annotated to Fanconi anemia complementation group N  (DOID:0111094)
  • 8 papers in RGD have been used to annotate PALB2
  • Curation Notes: ClinVar Annotator: match by term: Fanconi anemia complementation group N
  • Original References(s): PMID:19763884 PMID:20927582 PMID:21165770 PMID:21618343 PMID:24206657 PMID:24949998 PMID:25356972 PMID:25447460 PMID:25741868 PMID:26283626 PMID:26467025 PMID:28492532 PMID:28873162 PMID:35806449


    • An association has been curated linking PALB2 and Fanconi anemia complementation group N in Homo sapiens.        

  • The association was inferred from experiment (EXP)
    		•  
  • The annotation was made from RGD automated import pipeline for CTD gene-to-disease annotations
  • 1 RGD objects have been annotated to Fanconi anemia complementation group N  (DOID:0111094)
  • 8 papers in RGD have been used to annotate PALB2
  • Curation Notes: CTD Direct Evidence: marker/mechanism


    • An association has been curated linking PALB2 and Fanconi anemia complementation group N in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • 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 by association of genotype and phenotype with RGD:8591470 (Homo sapiens)
  • 1 RGD objects have been annotated to Fanconi anemia complementation group N  (DOID:0111094)
  • 8 papers in RGD have been used to annotate PALB2
  • Curation Notes: ClinVar Annotator: match by term: Fanconi anemia complementation group N
  • Original References(s): PMID:22241545 PMID:25741868 PMID:28492532


    • An association has been curated linking PALB2 and Fanconi anemia complementation group N in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • 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 by association of genotype and phenotype with RGD:8591404 (Homo sapiens)
  • 1 RGD objects have been annotated to Fanconi anemia complementation group N  (DOID:0111094)
  • 8 papers in RGD have been used to annotate PALB2
  • Curation Notes: ClinVar Annotator: match by term: Fanconi anemia complementation group N
  • Original References(s): PMID:17200668 PMID:18302019 PMID:18987736 PMID:19763884 PMID:20091115 PMID:20582465 PMID:20722467 PMID:20852946 PMID:21365267 PMID:21618343 PMID:21932393 PMID:22052327 PMID:22241545 PMID:23448497 PMID:23555315 PMID:23824750 PMID:23935836 PMID:24206657 PMID:24556926 PMID:24728327 PMID:24949998 PMID:25117502 PMID:25225577 PMID:25356972 PMID:25447460 PMID:25479140 PMID:25666743 PMID:25741868 PMID:25794774 PMID:26283626 PMID:26315354 PMID:26467025 PMID:26564480 PMID:26878173 PMID:27153395 PMID:28279176 PMID:28492532 PMID:31586400 PMID:31636395 PMID:31757951 PMID:33964450


    • An association has been curated linking PALB2 and Fanconi anemia complementation group N in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • 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 by association of genotype and phenotype with RGD:11091321 (Homo sapiens)
  • 1 RGD objects have been annotated to Fanconi anemia complementation group N  (DOID:0111094)
  • 8 papers in RGD have been used to annotate PALB2
  • Curation Notes: ClinVar Annotator: match by term: Fanconi anemia complementation group N
  • Original References(s): PMID:17200668 PMID:17200671 PMID:17200672 PMID:24136930 PMID:25099575 PMID:25741868 PMID:26315354 PMID:28492532 PMID:29470806 PMID:30128536 PMID:31263054 PMID:31428676 PMID:32885271


    • An association has been curated linking PALB2 and Fanconi anemia complementation group N in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • 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 by association of genotype and phenotype with RGD:8591469 (Homo sapiens)
  • 1 RGD objects have been annotated to Fanconi anemia complementation group N  (DOID:0111094)
  • 8 papers in RGD have been used to annotate PALB2
  • Curation Notes: ClinVar Annotator: match by term: Fanconi anemia complementation group N
  • Original References(s): PMID:17200668 PMID:17200671 PMID:19584259 PMID:19609323 PMID:21165770 PMID:21365267 PMID:22241545 PMID:23341105 PMID:25099575 PMID:25452441 PMID:25741868 PMID:26315354 PMID:26467025 PMID:26845104 PMID:28281021 PMID:28492532 PMID:31636395 PMID:32427313 PMID:32885271


    • An association has been curated linking PALB2 and Fanconi anemia complementation group N in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • 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 by association of genotype and phenotype with RGD:8591450 (Homo sapiens)
  • 1 RGD objects have been annotated to Fanconi anemia complementation group N  (DOID:0111094)
  • 8 papers in RGD have been used to annotate PALB2
  • Curation Notes: ClinVar Annotator: match by term: Fanconi anemia complementation group N
  • Original References(s): PMID:17200668 PMID:17200671 PMID:17200672 PMID:18302019 PMID:19264984 PMID:20412113 PMID:24136930 PMID:25099575 PMID:25452441 PMID:25741868 PMID:26283626 PMID:26467025 PMID:26845104 PMID:28492532 PMID:29909963 PMID:32885271 PMID:33471991 PMID:33917078 PMID:34113003


    • An association has been curated linking PALB2 and Fanconi anemia complementation group N in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • 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 by association of genotype and phenotype with RGD:9853977 (Homo sapiens)
  • 1 RGD objects have been annotated to Fanconi anemia complementation group N  (DOID:0111094)
  • 8 papers in RGD have been used to annotate PALB2
  • Curation Notes: ClinVar Annotator: match by term: Fanconi anemia complementation group N
  • Original References(s): PMID:25741868 PMID:26411315 PMID:27701467 PMID:28492532 PMID:28779002 PMID:28796317 PMID:30093976 PMID:30287823 PMID:32426482 PMID:32566746 PMID:32980694 PMID:33471991


    • An association has been curated linking PALB2 and Fanconi anemia complementation group N in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • 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 by association of genotype and phenotype with RGD:8595357 (Homo sapiens)
  • 1 RGD objects have been annotated to Fanconi anemia complementation group N  (DOID:0111094)
  • 8 papers in RGD have been used to annotate PALB2
  • Curation Notes: ClinVar Annotator: match by term: Fanconi anemia complementation group N
  • Original References(s): PMID:17200668 PMID:17200671 PMID:17200672 PMID:17924555 PMID:19264984 PMID:21285249 PMID:23935836 PMID:24136930 PMID:25099575 PMID:25525159 PMID:25583207 PMID:25741868 PMID:28319063 PMID:28492532 PMID:31446535 PMID:31636395 PMID:31757951 PMID:33471991


    • An association has been curated linking PALB2 and Fanconi anemia complementation group N in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • 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 by association of genotype and phenotype with RGD:8591433 (Homo sapiens)
  • 1 RGD objects have been annotated to Fanconi anemia complementation group N  (DOID:0111094)
  • 8 papers in RGD have been used to annotate PALB2
  • Curation Notes: ClinVar Annotator: match by term: Fanconi anemia complementation group N
  • Original References(s): PMID:21409391 PMID:23555315 PMID:24448499 PMID:25186627 PMID:25225577 PMID:25479140 PMID:25741868 PMID:26283626 PMID:26315354 PMID:26467025 PMID:26689913 PMID:26976419 PMID:28492532 PMID:28767289 PMID:28779002 PMID:28873162 PMID:30541756 PMID:32546565 PMID:32885271 PMID:33471991 PMID:35263119


    • An association has been curated linking PALB2 and Fanconi anemia complementation group N in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • 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 by association of genotype and phenotype with RGD:9834647 (Homo sapiens)
  • 1 RGD objects have been annotated to Fanconi anemia complementation group N  (DOID:0111094)
  • 8 papers in RGD have been used to annotate PALB2
  • Curation Notes: ClinVar Annotator: match by term: Fanconi anemia complementation group N
  • Original References(s): PMID:25741868 PMID:26467025 PMID:26681312 PMID:28492532 PMID:30890586 PMID:31589614


    • An association has been curated linking PALB2 and Fanconi anemia complementation group N in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • 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 by association of genotype and phenotype with RGD:9834644 (Homo sapiens)
  • 1 RGD objects have been annotated to Fanconi anemia complementation group N  (DOID:0111094)
  • 8 papers in RGD have been used to annotate PALB2
  • Curation Notes: ClinVar Annotator: match by term: Fanconi anemia complementation group N
  • Original References(s): PMID:17200668 PMID:17200671 PMID:17200672 PMID:24136930 PMID:25099575 PMID:25741868 PMID:28492532 PMID:31841383


    • An association has been curated linking PALB2 and Fanconi anemia complementation group N in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • 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 by association of genotype and phenotype with RGD:13472235 (Homo sapiens)
  • 1 RGD objects have been annotated to Fanconi anemia complementation group N  (DOID:0111094)
  • 8 papers in RGD have been used to annotate PALB2
  • Curation Notes: ClinVar Annotator: match by term: Fanconi anemia complementation group N
  • Original References(s): PMID:25741868 PMID:26411315 PMID:28492532 PMID:30287823 PMID:32426482


    • An association has been curated linking PALB2 and Fanconi anemia complementation group N in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • 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 by association of genotype and phenotype with RGD:8591418 (Homo sapiens)
  • 1 RGD objects have been annotated to Fanconi anemia complementation group N  (DOID:0111094)
  • 8 papers in RGD have been used to annotate PALB2
  • Curation Notes: ClinVar Annotator: match by term: Fanconi anemia complementation group N
  • Original References(s): PMID:17200668 PMID:18302019 PMID:19635604 PMID:20582465 PMID:20722467 PMID:21165770 PMID:21365267 PMID:21618343 PMID:22241545 PMID:23824750 PMID:23935836 PMID:24033266 PMID:24141787 PMID:24448499 PMID:24556926 PMID:24949998 PMID:25085752 PMID:25186627 PMID:25356972 PMID:25479140 PMID:25575445 PMID:25741868 PMID:26094658 PMID:26283626 PMID:26315354 PMID:26467025 PMID:26534844 PMID:26564480 PMID:26740942 PMID:27099641 PMID:27153395 PMID:27328445 PMID:27397723 PMID:27573125 PMID:27595995 PMID:27829436 PMID:28279176 PMID:28440294 PMID:28492532 PMID:29052111 PMID:29431189 PMID:30521987


    • An association has been curated linking PALB2 and Fanconi anemia complementation group N in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • 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 by association of genotype and phenotype with RGD:8591462 (Homo sapiens)
  • 1 RGD objects have been annotated to Fanconi anemia complementation group N  (DOID:0111094)
  • 8 papers in RGD have been used to annotate PALB2
  • Curation Notes: ClinVar Annotator: match by term: Fanconi anemia complementation group N
  • Original References(s): PMID:17200668 PMID:23824750 PMID:25085752 PMID:25741868 PMID:26315354 PMID:26467025 PMID:28492532 PMID:28779002 PMID:29522266 PMID:30287823 PMID:31422574 PMID:31586400 PMID:32048105 PMID:35263119


    • An association has been curated linking PALB2 and Fanconi anemia complementation group N in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • 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 by association of genotype and phenotype with RGD:8591434 (Homo sapiens)
  • 1 RGD objects have been annotated to Fanconi anemia complementation group N  (DOID:0111094)
  • 8 papers in RGD have been used to annotate PALB2
  • Curation Notes: ClinVar Annotator: match by term: Fanconi anemia complementation group N
  • Original References(s): PMID:17200668 PMID:18288683 PMID:18302019 PMID:18446436 PMID:19333784 PMID:20091115 PMID:20180015 PMID:20722467 PMID:20852946 PMID:20927582 PMID:21165770 PMID:21356067 PMID:21365267 PMID:21409391 PMID:21618343 PMID:21932393 PMID:22052327 PMID:22241545 PMID:22310028 PMID:22995991 PMID:23448497 PMID:23824750 PMID:23935836 PMID:24206657 PMID:24556926 PMID:24728327 PMID:24949998 PMID:25085752 PMID:25741868 PMID:26283626 PMID:28492532


    • An association has been curated linking PALB2 and Fanconi anemia complementation group N in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • 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 by association of genotype and phenotype with RGD:8591363 (Homo sapiens)
  • 1 RGD objects have been annotated to Fanconi anemia complementation group N  (DOID:0111094)
  • 8 papers in RGD have been used to annotate PALB2
  • Curation Notes: ClinVar Annotator: match by term: Fanconi anemia complementation group N
  • Original References(s): PMID:21618343 PMID:23448497 PMID:25741868 PMID:26467025 PMID:28492532


    • An association has been curated linking PALB2 and Fanconi anemia complementation group N in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • 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 by association of genotype and phenotype with RGD:9851251 (Homo sapiens)
  • 1 RGD objects have been annotated to Fanconi anemia complementation group N  (DOID:0111094)
  • 8 papers in RGD have been used to annotate PALB2
  • Curation Notes: ClinVar Annotator: match by term: Fanconi anemia complementation group N
  • Original References(s): PMID:17200668 PMID:21618343 PMID:25741868 PMID:26467025 PMID:28492532 PMID:28779002 PMID:30287823


    • An association has been curated linking PALB2 and Fanconi anemia complementation group N in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • 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 by association of genotype and phenotype with RGD:8591504 (Homo sapiens)
  • 1 RGD objects have been annotated to Fanconi anemia complementation group N  (DOID:0111094)
  • 8 papers in RGD have been used to annotate PALB2
  • Curation Notes: ClinVar Annotator: match by term: Fanconi anemia complementation group N
  • Original References(s): PMID:17200668 PMID:17200671 PMID:17200672 PMID:21932393 PMID:22692731 PMID:23110154 PMID:23824750 PMID:24136930 PMID:24448499 PMID:24763289 PMID:24870022 PMID:25099575 PMID:25428789 PMID:25741868 PMID:25980754 PMID:26283626 PMID:26467025 PMID:26689913 PMID:26786923 PMID:28194609 PMID:28492532 PMID:28779002 PMID:30287823 PMID:30322717 PMID:32854451 PMID:33471991


    • An association has been curated linking PALB2 and Fanconi anemia complementation group N in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • 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 by association of genotype and phenotype with RGD:10768258|RGD:11091941|RGD:12890447|RGD:9834679|RGD:9851587|RGD:9851666 (Homo sapiens) & RGD:10768258|RGD:11091941|RGD:12890447|RGD:9834679|RGD:9851587|RGD:9851666 (Homo sapiens) & RGD:10768258|RGD:11091941|RGD:12890447|RGD:9834679|RGD:9851587|RGD:9851666 (Homo sapiens) & RGD:10768258|RGD:11091941|RGD:12890447|RGD:9834679|RGD:9851587|RGD:9851666 (Homo sapiens) & RGD:10768258|RGD:11091941|RGD:12890447|RGD:9834679|RGD:9851587|RGD:9851666 (Homo sapiens) & RGD:10768258|RGD:11091941|RGD:12890447|RGD:9834679|RGD:9851587|RGD:9851666 (Homo sapiens)
  • 1 RGD objects have been annotated to Fanconi anemia complementation group N  (DOID:0111094)
  • 8 papers in RGD have been used to annotate PALB2
  • Curation Notes: ClinVar Annotator: match by term: Fanconi anemia complementation group N
  • Original References(s): PMID:25741868 PMID:26467025 PMID:28492532


    • An association has been curated linking PALB2 and Fanconi anemia complementation group N in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • 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 by association of genotype and phenotype with RGD:26888076 (Homo sapiens)
  • 1 RGD objects have been annotated to Fanconi anemia complementation group N  (DOID:0111094)
  • 8 papers in RGD have been used to annotate PALB2
  • Curation Notes: ClinVar Annotator: match by term: Fanconi anemia complementation group N
  • Original References(s): PMID:23977390 PMID:25741868 PMID:28492532 PMID:31586400


    • An association has been curated linking PALB2 and Fanconi anemia complementation group N in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • 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 by association of genotype and phenotype with RGD:11089130|RGD:11093599|RGD:12841766|RGD:12843480|RGD:13476401|RGD:13510431|RGD:13512629|RGD:13802936|RGD:13815939|RGD:28893245|RGD:405083279|RGD:8689919|RGD:9850635|RGD:9854114|RGD:9854237 (Homo sapiens) & RGD:11089130|RGD:11093599|RGD:12841766|RGD:12843480|RGD:13476401|RGD:13510431|RGD:13512629|RGD:13802936|RGD:13815939|RGD:28893245|RGD:405083279|RGD:8689919|RGD:9850635|RGD:9854114|RGD:9854237 (Homo sapiens) & RGD:11089130|RGD:11093599|RGD:12841766|RGD:12843480|RGD:13476401|RGD:13510431|RGD:13512629|RGD:13802936|RGD:13815939|RGD:28893245|RGD:405083279|RGD:8689919|RGD:9850635|RGD:9854114|RGD:9854237 (Homo sapiens) & RGD:11089130|RGD:11093599|RGD:12841766|RGD:12843480|RGD:13476401|RGD:13510431|RGD:13512629|RGD:13802936|RGD:13815939|RGD:28893245|RGD:405083279|RGD:8689919|RGD:9850635|RGD:9854114|RGD:9854237 (Homo sapiens) & RGD:11089130|RGD:11093599|RGD:12841766|RGD:12843480|RGD:13476401|RGD:13510431|RGD:13512629|RGD:13802936|RGD:13815939|RGD:28893245|RGD:405083279|RGD:8689919|RGD:9850635|RGD:9854114|RGD:9854237 (Homo sapiens) & RGD:11089130|RGD:11093599|RGD:12841766|RGD:12843480|RGD:13476401|RGD:13510431|RGD:13512629|RGD:13802936|RGD:13815939|RGD:28893245|RGD:405083279|RGD:8689919|RGD:9850635|RGD:9854114|RGD:9854237 (Homo sapiens) & RGD:11089130|RGD:11093599|RGD:12841766|RGD:12843480|RGD:13476401|RGD:13510431|RGD:13512629|RGD:13802936|RGD:13815939|RGD:28893245|RGD:405083279|RGD:8689919|RGD:9850635|RGD:9854114|RGD:9854237 (Homo sapiens) & RGD:11089130|RGD:11093599|RGD:12841766|RGD:12843480|RGD:13476401|RGD:13510431|RGD:13512629|RGD:13802936|RGD:13815939|RGD:28893245|RGD:405083279|RGD:8689919|RGD:9850635|RGD:9854114|RGD:9854237 (Homo sapiens) & RGD:11089130|RGD:11093599|RGD:12841766|RGD:12843480|RGD:13476401|RGD:13510431|RGD:13512629|RGD:13802936|RGD:13815939|RGD:28893245|RGD:405083279|RGD:8689919|RGD:9850635|RGD:9854114|RGD:9854237 (Homo sapiens) & RGD:11089130|RGD:11093599|RGD:12841766|RGD:12843480|RGD:13476401|RGD:13510431|RGD:13512629|RGD:13802936|RGD:13815939|RGD:28893245|RGD:405083279|RGD:8689919|RGD:9850635|RGD:9854114|RGD:9854237 (Homo sapiens) & RGD:11089130|RGD:11093599|RGD:12841766|RGD:12843480|RGD:13476401|RGD:13510431|RGD:13512629|RGD:13802936|RGD:13815939|RGD:28893245|RGD:405083279|RGD:8689919|RGD:9850635|RGD:9854114|RGD:9854237 (Homo sapiens) & RGD:11089130|RGD:11093599|RGD:12841766|RGD:12843480|RGD:13476401|RGD:13510431|RGD:13512629|RGD:13802936|RGD:13815939|RGD:28893245|RGD:405083279|RGD:8689919|RGD:9850635|RGD:9854114|RGD:9854237 (Homo sapiens) & RGD:11089130|RGD:11093599|RGD:12841766|RGD:12843480|RGD:13476401|RGD:13510431|RGD:13512629|RGD:13802936|RGD:13815939|RGD:28893245|RGD:405083279|RGD:8689919|RGD:9850635|RGD:9854114|RGD:9854237 (Homo sapiens) & RGD:11089130|RGD:11093599|RGD:12841766|RGD:12843480|RGD:13476401|RGD:13510431|RGD:13512629|RGD:13802936|RGD:13815939|RGD:28893245|RGD:405083279|RGD:8689919|RGD:9850635|RGD:9854114|RGD:9854237 (Homo sapiens) & RGD:11089130|RGD:11093599|RGD:12841766|RGD:12843480|RGD:13476401|RGD:13510431|RGD:13512629|RGD:13802936|RGD:13815939|RGD:28893245|RGD:405083279|RGD:8689919|RGD:9850635|RGD:9854114|RGD:9854237 (Homo sapiens)
  • 1 RGD objects have been annotated to Fanconi anemia complementation group N  (DOID:0111094)
  • 8 papers in RGD have been used to annotate PALB2
  • Curation Notes: ClinVar Annotator: match by term: Fanconi anemia complementation group N
  • Original References(s): PMID:25741868 PMID:28492532


    • An association has been curated linking PALB2 and Fanconi anemia complementation group N in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • 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 by association of genotype and phenotype with RGD:12893057 (Homo sapiens)
  • 1 RGD objects have been annotated to Fanconi anemia complementation group N  (DOID:0111094)
  • 8 papers in RGD have been used to annotate PALB2
  • Curation Notes: ClinVar Annotator: match by term: Fanconi anemia complementation group N
  • Original References(s): PMID:25741868 PMID:28492532 PMID:28779002 PMID:28825143 PMID:30287823 PMID:31214711 PMID:33471991 PMID:34034685


    • An association has been curated linking PALB2 and Fanconi anemia complementation group N in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • 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 by association of genotype and phenotype with RGD:10407735 (Homo sapiens)
  • 1 RGD objects have been annotated to Fanconi anemia complementation group N  (DOID:0111094)
  • 8 papers in RGD have been used to annotate PALB2
  • Curation Notes: ClinVar Annotator: match by term: Fanconi anemia complementation group N
  • Original References(s): PMID:23555315 PMID:25085752 PMID:25741868 PMID:26467025 PMID:28492532 PMID:28873162 PMID:32832836 PMID:32868316


    • An association has been curated linking PALB2 and Fanconi anemia complementation group N in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • 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 by association of genotype and phenotype with RGD:11346544 (Homo sapiens)
  • 1 RGD objects have been annotated to Fanconi anemia complementation group N  (DOID:0111094)
  • 8 papers in RGD have been used to annotate PALB2
  • Curation Notes: ClinVar Annotator: match by term: Fanconi anemia complementation group N
  • Original References(s): PMID:17200668 PMID:17200671 PMID:17200672 PMID:24136930 PMID:25099575 PMID:25741868 PMID:26023681 PMID:28492532 PMID:29625052 PMID:29785153 PMID:31159747 PMID:31447099 PMID:31619740


    • An association has been curated linking PALB2 and Fanconi anemia complementation group N in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • 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 by association of genotype and phenotype with RGD:12882311|RGD:14744566|RGD:25317861|RGD:9852708|RGD:9853532 (Homo sapiens) & RGD:12882311|RGD:14744566|RGD:25317861|RGD:9852708|RGD:9853532 (Homo sapiens) & RGD:12882311|RGD:14744566|RGD:25317861|RGD:9852708|RGD:9853532 (Homo sapiens) & RGD:12882311|RGD:14744566|RGD:25317861|RGD:9852708|RGD:9853532 (Homo sapiens) & RGD:12882311|RGD:14744566|RGD:25317861|RGD:9852708|RGD:9853532 (Homo sapiens)
  • 1 RGD objects have been annotated to Fanconi anemia complementation group N  (DOID:0111094)
  • 8 papers in RGD have been used to annotate PALB2
  • Curation Notes: ClinVar Annotator: match by term: Fanconi anemia complementation group N
  • Original References(s): PMID:25741868 PMID:28492532 PMID:30287823


    • An association has been curated linking PALB2 and Fanconi anemia complementation group N in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • 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 by association of genotype and phenotype with RGD:8658543 (Homo sapiens)
  • 1 RGD objects have been annotated to Fanconi anemia complementation group N  (DOID:0111094)
  • 8 papers in RGD have been used to annotate PALB2
  • Curation Notes: ClinVar Annotator: match by term: Fanconi anemia complementation group N
  • Original References(s): PMID:17200668 PMID:17200671 PMID:17200672 PMID:20412113 PMID:21165770 PMID:21285249 PMID:21618343 PMID:22692731 PMID:24136930 PMID:24448499 PMID:25099575 PMID:25186627 PMID:25741868 PMID:26467025 PMID:26681312 PMID:26720728 PMID:27449771 PMID:27553368 PMID:28492532 PMID:28528518 PMID:28724667 PMID:29470806 PMID:30067863 PMID:30128536 PMID:31467304 PMID:31619740 PMID:33471991 PMID:36988593


    • An association has been curated linking PALB2 and Fanconi anemia complementation group N in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • 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 by association of genotype and phenotype with RGD:8591453 (Homo sapiens)
  • 1 RGD objects have been annotated to Fanconi anemia complementation group N  (DOID:0111094)
  • 8 papers in RGD have been used to annotate PALB2
  • Curation Notes: ClinVar Annotator: match by term: Fanconi anemia complementation group N
  • Original References(s): PMID:22241545 PMID:25741868 PMID:28492532 PMID:28779002 PMID:30287823 PMID:30651582 PMID:31214711 PMID:31721781 PMID:32980694 PMID:33471991 PMID:34284872 PMID:37013556


    • An association has been curated linking PALB2 and Fanconi anemia complementation group N in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • 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 by association of genotype and phenotype with RGD:8591358 (Homo sapiens)
  • 1 RGD objects have been annotated to Fanconi anemia complementation group N  (DOID:0111094)
  • 8 papers in RGD have been used to annotate PALB2
  • Curation Notes: ClinVar Annotator: match by term: Fanconi anemia complementation group N
  • Original References(s): PMID:22241545 PMID:25186627 PMID:25741868 PMID:26283626 PMID:26315354 PMID:26467025 PMID:28492532 PMID:31843900 PMID:33471991 PMID:35263119


    • An association has been curated linking PALB2 and Fanconi anemia complementation group N in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • 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 by association of genotype and phenotype with RGD:8591505 (Homo sapiens)
  • 1 RGD objects have been annotated to Fanconi anemia complementation group N  (DOID:0111094)
  • 8 papers in RGD have been used to annotate PALB2
  • Curation Notes: ClinVar Annotator: match by term: Fanconi anemia complementation group N
  • Original References(s): PMID:17200668 PMID:18302019 PMID:25741868 PMID:26467025 PMID:26564480 PMID:28492532


    • An association has been curated linking PALB2 and Fanconi anemia complementation group N in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • 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 by association of genotype and phenotype with RGD:8591426 (Homo sapiens)
  • 1 RGD objects have been annotated to Fanconi anemia complementation group N  (DOID:0111094)
  • 8 papers in RGD have been used to annotate PALB2
  • Curation Notes: ClinVar Annotator: match by term: Fanconi anemia complementation group N
  • Original References(s): PMID:21932393 PMID:23555315 PMID:23824750 PMID:24728327 PMID:25741868 PMID:26467025 PMID:28492532 PMID:31206626


    • An association has been curated linking PALB2 and Fanconi anemia complementation group N in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • 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 by association of genotype and phenotype with RGD:9852725 (Homo sapiens)
  • 1 RGD objects have been annotated to Fanconi anemia complementation group N  (DOID:0111094)
  • 8 papers in RGD have been used to annotate PALB2
  • Curation Notes: ClinVar Annotator: match by term: Fanconi anemia complementation group N
  • Original References(s): PMID:23977390 PMID:25741868 PMID:26283626 PMID:26467025 PMID:28492532 PMID:30287823 PMID:31214711


    • An association has been curated linking PALB2 and Fanconi anemia complementation group N in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • 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 by association of genotype and phenotype with RGD:8591475 (Homo sapiens)
  • 1 RGD objects have been annotated to Fanconi anemia complementation group N  (DOID:0111094)
  • 8 papers in RGD have been used to annotate PALB2
  • Curation Notes: ClinVar Annotator: match by term: Fanconi anemia complementation group N
  • Original References(s): PMID:20852946 PMID:22692731 PMID:24448499 PMID:24556926 PMID:25085752 PMID:25186627 PMID:25479140 PMID:25741868 PMID:26283626 PMID:26315354 PMID:26467025 PMID:26564480 PMID:26898890 PMID:27878467 PMID:28492532 PMID:28779002 PMID:28944238 PMID:29522266 PMID:30306255 PMID:31206626 PMID:31451522 PMID:31512090 PMID:31757951 PMID:32658311 PMID:33195396 PMID:33320972 PMID:33471991 PMID:33558524 PMID:33630411 PMID:33980423 PMID:34426522 PMID:34478935 PMID:36605468


    • An association has been curated linking PALB2 and Fanconi anemia complementation group N in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • 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 by association of genotype and phenotype with RGD:13619595 (Homo sapiens)
  • 1 RGD objects have been annotated to Fanconi anemia complementation group N  (DOID:0111094)
  • 8 papers in RGD have been used to annotate PALB2
  • Curation Notes: ClinVar Annotator: match by term: Fanconi anemia complementation group N
  • Original References(s): PMID:25741868 PMID:26467025 PMID:28492532 PMID:33471991


    • An association has been curated linking PALB2 and Fanconi anemia complementation group N in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • 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 by association of genotype and phenotype with RGD:9851544 (Homo sapiens)
  • 1 RGD objects have been annotated to Fanconi anemia complementation group N  (DOID:0111094)
  • 8 papers in RGD have been used to annotate PALB2
  • Curation Notes: ClinVar Annotator: match by term: Fanconi anemia complementation group N
  • Original References(s): PMID:25741868 PMID:26283626 PMID:26315354 PMID:26411315 PMID:26467025 PMID:26689913 PMID:27621404 PMID:28492532 PMID:28796317 PMID:29667044 PMID:29802286 PMID:30287823 PMID:31206626 PMID:31214711 PMID:32426482 PMID:32566746 PMID:33309985 PMID:33471991 PMID:34608183


    • An association has been curated linking PALB2 and Fanconi anemia complementation group N in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • 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 by association of genotype and phenotype with RGD:8591516 (Homo sapiens)
  • 1 RGD objects have been annotated to Fanconi anemia complementation group N  (DOID:0111094)
  • 8 papers in RGD have been used to annotate PALB2
  • Curation Notes: ClinVar Annotator: match by term: Fanconi anemia complementation group N
  • Original References(s): PMID:23448497 PMID:24728327 PMID:25085752 PMID:25186627 PMID:25503501 PMID:25741868 PMID:25980754 PMID:26283626 PMID:26467025 PMID:27153395 PMID:28492532 PMID:28779002 PMID:31586400 PMID:33471991 PMID:34687117


    • An association has been curated linking PALB2 and Fanconi anemia complementation group N in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • 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 by association of genotype and phenotype with RGD:8658555 (Homo sapiens)
  • 1 RGD objects have been annotated to Fanconi anemia complementation group N  (DOID:0111094)
  • 8 papers in RGD have been used to annotate PALB2
  • Curation Notes: ClinVar Annotator: match by term: Fanconi anemia complementation group N
  • Original References(s): PMID:24556926 PMID:25741868 PMID:26283626 PMID:26467025 PMID:26564480 PMID:27106063 PMID:28492532 PMID:28779002 PMID:28794409 PMID:31642931 PMID:35264596 PMID:35806449


    • An association has been curated linking PALB2 and Fanconi anemia complementation group N in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • 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 by association of genotype and phenotype with RGD:8591373 (Homo sapiens)
  • 1 RGD objects have been annotated to Fanconi anemia complementation group N  (DOID:0111094)
  • 8 papers in RGD have been used to annotate PALB2
  • Curation Notes: ClinVar Annotator: match by term: Fanconi anemia complementation group N
  • Original References(s): PMID:20122277 PMID:20589654 PMID:21618343 PMID:22241545 PMID:22692731 PMID:25085752 PMID:25356972 PMID:25741868 PMID:25980754 PMID:26283626 PMID:26315354 PMID:26467025 PMID:28051113 PMID:28492532 PMID:29052111 PMID:30995915 PMID:33471991 PMID:33964450 PMID:35264596


    • An association has been curated linking PALB2 and Fanconi anemia complementation group N in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • 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 by association of genotype and phenotype with RGD:8697137 (Homo sapiens)
  • 1 RGD objects have been annotated to Fanconi anemia complementation group N  (DOID:0111094)
  • 8 papers in RGD have been used to annotate PALB2
  • Curation Notes: ClinVar Annotator: match by term: Fanconi anemia complementation group N
  • Original References(s): PMID:17200668 PMID:17200671 PMID:17200672 PMID:23977390 PMID:24136930 PMID:24556926 PMID:24763289 PMID:25099575 PMID:25741868 PMID:26467025 PMID:28135048 PMID:28492532 PMID:29431189 PMID:29522266 PMID:30128536 PMID:30287823 PMID:31054147 PMID:31263054 PMID:31428676 PMID:32339256 PMID:33193564 PMID:33471991 PMID:33811135


    • An association has been curated linking PALB2 and Fanconi anemia complementation group N in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • 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 by association of genotype and phenotype with RGD:8591464 (Homo sapiens)
  • 1 RGD objects have been annotated to Fanconi anemia complementation group N  (DOID:0111094)
  • 8 papers in RGD have been used to annotate PALB2
  • Curation Notes: ClinVar Annotator: match by term: Fanconi anemia complementation group N
  • Original References(s): PMID:17200668 PMID:17200671 PMID:17200672 PMID:19264984 PMID:21165770 PMID:23561644 PMID:23935836 PMID:24136930 PMID:25099575 PMID:25356972 PMID:25741868 PMID:26283626 PMID:26315354 PMID:26467025 PMID:26681312 PMID:26720728 PMID:26845104 PMID:28492532 PMID:28724667 PMID:28779002 PMID:29752822 PMID:30720863 PMID:31841383 PMID:32068069 PMID:32566746 PMID:32853339 PMID:33169439 PMID:33471991 PMID:34439348 PMID:36988593


    • An association has been curated linking PALB2 and Fanconi anemia complementation group N in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • 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 by association of genotype and phenotype with RGD:11346974 (Homo sapiens)
  • 1 RGD objects have been annotated to Fanconi anemia complementation group N  (DOID:0111094)
  • 8 papers in RGD have been used to annotate PALB2
  • Curation Notes: ClinVar Annotator: match by term: Fanconi anemia complementation group N
  • Original References(s): PMID:16793542 PMID:19369211 PMID:25099575 PMID:26649820 PMID:28319063 PMID:28492532 PMID:30337689 PMID:31173646 PMID:31263571 PMID:31586400 PMID:31871297 PMID:35626031


    • An association has been curated linking PALB2 and Fanconi anemia complementation group N in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • 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 by association of genotype and phenotype with RGD:13496947 (Homo sapiens)
  • 1 RGD objects have been annotated to Fanconi anemia complementation group N  (DOID:0111094)
  • 8 papers in RGD have been used to annotate PALB2
  • Curation Notes: ClinVar Annotator: match by term: Fanconi anemia complementation group N
  • Original References(s): PMID:25741868 PMID:26467025 PMID:28492532 PMID:28828701 PMID:28873162 PMID:31206626 PMID:33471991 PMID:33558524


    • An association has been curated linking PALB2 and Fanconi anemia complementation group N in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • 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 by association of genotype and phenotype with RGD:8591384 (Homo sapiens)
  • 1 RGD objects have been annotated to Fanconi anemia complementation group N  (DOID:0111094)
  • 8 papers in RGD have been used to annotate PALB2
  • Curation Notes: ClinVar Annotator: match by term: Fanconi anemia complementation group N
  • Original References(s): PMID:17200668 PMID:17200671 PMID:17200672 PMID:19264984 PMID:19763819 PMID:20852946 PMID:20858716 PMID:21285249 PMID:23935381 PMID:24136930 PMID:24415441 PMID:24549055 PMID:25099575 PMID:25741868 PMID:26283626 PMID:26467025 PMID:26489409 PMID:26786923 PMID:28492532 PMID:28767289 PMID:29431189 PMID:33471991


    • An association has been curated linking PALB2 and Fanconi anemia complementation group N in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • 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 by association of genotype and phenotype with RGD:10042195 (Homo sapiens)
  • 1 RGD objects have been annotated to Fanconi anemia complementation group N  (DOID:0111094)
  • 8 papers in RGD have been used to annotate PALB2
  • Curation Notes: ClinVar Annotator: match by term: Fanconi anemia complementation group N
  • Original References(s): PMID:21618343 PMID:25741868 PMID:28492532 PMID:31586400 PMID:32546565 PMID:32658311 PMID:33471991 PMID:35089076


    • An association has been curated linking PALB2 and Fanconi anemia complementation group N in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • 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 by association of genotype and phenotype with RGD:9834633 (Homo sapiens)
  • 1 RGD objects have been annotated to Fanconi anemia complementation group N  (DOID:0111094)
  • 8 papers in RGD have been used to annotate PALB2
  • Curation Notes: ClinVar Annotator: match by term: Fanconi anemia complementation group N
  • Original References(s): PMID:17200668 PMID:17200671 PMID:17200672 PMID:24136930 PMID:25099575 PMID:25741868 PMID:26467025 PMID:26681312 PMID:28492532 PMID:28724667 PMID:29506128 PMID:31768816 PMID:36988593


    • An association has been curated linking PALB2 and Fanconi anemia complementation group N in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • 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 by association of genotype and phenotype with RGD:8591407 (Homo sapiens)
  • 1 RGD objects have been annotated to Fanconi anemia complementation group N  (DOID:0111094)
  • 8 papers in RGD have been used to annotate PALB2
  • Curation Notes: ClinVar Annotator: match by term: Fanconi anemia complementation group N
  • Original References(s): PMID:17200668 PMID:22241545 PMID:25085752 PMID:25186627 PMID:25356972 PMID:25575445 PMID:25741868 PMID:25980754 PMID:26283626 PMID:26315354 PMID:26467025 PMID:26534844 PMID:26689913 PMID:28492532 PMID:28503720 PMID:28779002 PMID:29368341 PMID:30113427 PMID:30287823 PMID:30982232 PMID:31214711 PMID:31742824 PMID:32830346 PMID:32853339 PMID:32980694 PMID:33471991


    • An association has been curated linking PALB2 and Fanconi anemia complementation group N in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • 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 by association of genotype and phenotype with RGD:9853647 (Homo sapiens)
  • 1 RGD objects have been annotated to Fanconi anemia complementation group N  (DOID:0111094)
  • 8 papers in RGD have been used to annotate PALB2
  • Curation Notes: ClinVar Annotator: match by term: Fanconi anemia complementation group N
  • Original References(s): PMID:25085752 PMID:25741868 PMID:26689913 PMID:28492532 PMID:28779002 PMID:28944238 PMID:33471991 PMID:35610400


    • An association has been curated linking PALB2 and Fanconi anemia complementation group N in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • 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 by association of genotype and phenotype with RGD:8591492 (Homo sapiens)
  • 1 RGD objects have been annotated to Fanconi anemia complementation group N  (DOID:0111094)
  • 8 papers in RGD have been used to annotate PALB2
  • Curation Notes: ClinVar Annotator: match by term: Fanconi anemia complementation group N
  • Original References(s): PMID:17200668 PMID:17200671 PMID:17200672 PMID:20122277 PMID:20412113 PMID:20582465 PMID:20589654 PMID:21165770 PMID:21285249 PMID:21365267 PMID:24061862 PMID:24136930 PMID:24415441 PMID:25099575 PMID:25186627 PMID:25330149 PMID:25452441 PMID:25741868 PMID:25959805 PMID:26083025 PMID:26270727 PMID:26467025 PMID:26689913 PMID:26720728 PMID:26845104 PMID:27038244 PMID:27099641 PMID:27106063 PMID:28158555 PMID:28279176 PMID:28492532 PMID:28709830 PMID:29052111 PMID:29478780 PMID:29625052 PMID:30086788 PMID:30113427 PMID:30833416 PMID:31159747 PMID:31312277 PMID:31570822 PMID:32295079 PMID:32546565 PMID:32554798 PMID:32853339 PMID:32885271 PMID:32997802 PMID:33471991 PMID:33674644


    • An association has been curated linking PALB2 and Fanconi anemia complementation group N in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • 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 by association of genotype and phenotype with RGD:11094354 (Homo sapiens)
  • 1 RGD objects have been annotated to Fanconi anemia complementation group N  (DOID:0111094)
  • 8 papers in RGD have been used to annotate PALB2
  • Curation Notes: ClinVar Annotator: match by term: Fanconi anemia complementation group N
  • Original References(s): PMID:25741868 PMID:27106063 PMID:28492532 PMID:29522266 PMID:30303537 PMID:30680046 PMID:31636395 PMID:33471991


    • An association has been curated linking PALB2 and Fanconi anemia complementation group N in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • 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 by association of genotype and phenotype with RGD:10448870 (Homo sapiens)
  • 1 RGD objects have been annotated to Fanconi anemia complementation group N  (DOID:0111094)
  • 8 papers in RGD have been used to annotate PALB2
  • Curation Notes: ClinVar Annotator: match by term: Fanconi anemia complementation group N
  • Original References(s): PMID:21618343 PMID:25741868 PMID:27930734 PMID:27978560 PMID:28492532 PMID:29522266 PMID:31159747 PMID:31586400 PMID:31636395 PMID:33471991 PMID:33964450 PMID:33980423


    • An association has been curated linking PALB2 and Fanconi anemia complementation group N in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • 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 by association of genotype and phenotype with RGD:8595359 (Homo sapiens)
  • 1 RGD objects have been annotated to Fanconi anemia complementation group N  (DOID:0111094)
  • 8 papers in RGD have been used to annotate PALB2
  • Curation Notes: ClinVar Annotator: match by term: Fanconi anemia complementation group N
  • Original References(s): PMID:17200668 PMID:17200671 PMID:17200672 PMID:19264984 PMID:21365267 PMID:21618343 PMID:24136930 PMID:25099575 PMID:25525159 PMID:25741868 PMID:28152038 PMID:28492532 PMID:28779002 PMID:33471991


    • An association has been curated linking PALB2 and Fanconi anemia complementation group N in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • 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 by association of genotype and phenotype with RGD:8698013 (Homo sapiens)
  • 1 RGD objects have been annotated to Fanconi anemia complementation group N  (DOID:0111094)
  • 8 papers in RGD have been used to annotate PALB2
  • Curation Notes: ClinVar Annotator: match by term: Fanconi anemia complementation group N
  • Original References(s): PMID:17200668 PMID:17200671 PMID:17200672 PMID:19264984 PMID:19763884 PMID:20852946 PMID:21618343 PMID:24033266 PMID:24136930 PMID:25099575 PMID:25186627 PMID:25452441 PMID:25741868 PMID:26467025 PMID:27783279 PMID:27798748 PMID:28152038 PMID:28423363 PMID:28486781 PMID:28492532 PMID:28724667 PMID:28779002 PMID:29093764 PMID:29338689 PMID:29566657 PMID:29752822 PMID:29915322 PMID:30287823 PMID:30303537 PMID:30306255 PMID:30982232 PMID:31089269 PMID:31300551 PMID:31786208 PMID:32339256 PMID:32832836 PMID:32854451 PMID:32885271 PMID:33169439 PMID:33471991 PMID:36605468 PMID:36988593


    • An association has been curated linking PALB2 and Fanconi anemia complementation group N in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • 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 by association of genotype and phenotype with RGD:8697395 (Homo sapiens)
  • 1 RGD objects have been annotated to Fanconi anemia complementation group N  (DOID:0111094)
  • 8 papers in RGD have been used to annotate PALB2
  • Curation Notes: ClinVar Annotator: match by term: Fanconi anemia complementation group N
  • Original References(s): PMID:25085752 PMID:25741868 PMID:26283626 PMID:26315354 PMID:26467025 PMID:26580448 PMID:28492532 PMID:33471991


    • An association has been curated linking PALB2 and Fanconi anemia complementation group N in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • 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 by association of genotype and phenotype with RGD:8595358 (Homo sapiens)
  • 1 RGD objects have been annotated to Fanconi anemia complementation group N  (DOID:0111094)
  • 8 papers in RGD have been used to annotate PALB2
  • Curation Notes: ClinVar Annotator: match by term: Fanconi anemia complementation group N
  • Original References(s): PMID:17200668 PMID:17200671 PMID:19264984 PMID:19584259 PMID:19609323 PMID:20927582 PMID:21165770 PMID:21365267 PMID:22241545 PMID:24415441 PMID:24728327 PMID:24949998 PMID:25099575 PMID:25225577 PMID:25452441 PMID:25741868 PMID:26283626 PMID:26296701 PMID:26315354 PMID:26467025 PMID:26641009 PMID:26681312 PMID:26845104 PMID:26898890 PMID:27356891 PMID:28008555 PMID:28492532 PMID:28779002 PMID:29360161 PMID:29753700 PMID:30322717 PMID:31159747 PMID:31575519 PMID:31757951 PMID:32012241 PMID:32339256 PMID:32546565 PMID:34113003


    • An association has been curated linking PALB2 and Fanconi anemia complementation group N in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • 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 by association of genotype and phenotype with RGD:8696866 (Homo sapiens)
  • 1 RGD objects have been annotated to Fanconi anemia complementation group N  (DOID:0111094)
  • 8 papers in RGD have been used to annotate PALB2
  • Curation Notes: ClinVar Annotator: match by term: Fanconi anemia complementation group N
  • Original References(s): PMID:25741868 PMID:28492532 PMID:30306255 PMID:30982232 PMID:31636395 PMID:33471991 PMID:35264596


    • An association has been curated linking PALB2 and Fanconi anemia complementation group N in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • 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 by association of genotype and phenotype with RGD:8591446 (Homo sapiens)
  • 1 RGD objects have been annotated to Fanconi anemia complementation group N  (DOID:0111094)
  • 8 papers in RGD have been used to annotate PALB2
  • Curation Notes: ClinVar Annotator: match by term: Fanconi anemia complementation group N
  • Original References(s): PMID:100849 PMID:17200668 PMID:18302019 PMID:19264984 PMID:21182766 PMID:21285249 PMID:21409391 PMID:22241545 PMID:23448497 PMID:23471749 PMID:23787919 PMID:24206657 PMID:24415441 PMID:25099575 PMID:25225577 PMID:25356972 PMID:25525159 PMID:25575445 PMID:25741868 PMID:26283626 PMID:26315354 PMID:26467025 PMID:26534844 PMID:26681312 PMID:26689913 PMID:26845104 PMID:27433846 PMID:27595995 PMID:28158555 PMID:28492532 PMID:28779002 PMID:28864920 PMID:29431189 PMID:29625052 PMID:29909963 PMID:29961768 PMID:30322717 PMID:30665703 PMID:31090900 PMID:31263054 PMID:31447099 PMID:31757951 PMID:31843900 PMID:32081490 PMID:32338768 PMID:32426482 PMID:32581362 PMID:32832836 PMID:32853339 PMID:33471991


    • An association has been curated linking PALB2 and Fanconi anemia complementation group N in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • 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 by association of genotype and phenotype with RGD:11523339 (Homo sapiens)
  • 1 RGD objects have been annotated to Fanconi anemia complementation group N  (DOID:0111094)
  • 8 papers in RGD have been used to annotate PALB2
  • Curation Notes: ClinVar Annotator: match by term: Fanconi anemia complementation group N
  • Original References(s): PMID:17200668 PMID:17200671 PMID:17200672 PMID:24136930 PMID:25099575 PMID:25741868 PMID:28492532 PMID:33471991


    • An association has been curated linking PALB2 and Fanconi anemia complementation group N in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • 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 by association of genotype and phenotype with RGD:8591483 (Homo sapiens)
  • 1 RGD objects have been annotated to Fanconi anemia complementation group N  (DOID:0111094)
  • 8 papers in RGD have been used to annotate PALB2
  • Curation Notes: ClinVar Annotator: match by term: Fanconi anemia complementation group N
  • Original References(s): PMID:17200668 PMID:17200671 PMID:19264984 PMID:24136930 PMID:25099575 PMID:28492532


    • An association has been curated linking PALB2 and Fanconi anemia complementation group N in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • 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 by association of genotype and phenotype with RGD:26888107|RGD:8591386 (Homo sapiens) & RGD:26888107|RGD:8591386 (Homo sapiens)
  • 1 RGD objects have been annotated to Fanconi anemia complementation group N  (DOID:0111094)
  • 8 papers in RGD have been used to annotate PALB2
  • Curation Notes: ClinVar Annotator: match by term: Fanconi anemia complementation group N
  • Original References(s): PMID:17200671 PMID:19264984


    • An association has been curated linking PALB2 and Fanconi anemia complementation group N in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • 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 by association of genotype and phenotype with RGD:11613761 (Homo sapiens)
  • 1 RGD objects have been annotated to Fanconi anemia complementation group N  (DOID:0111094)
  • 8 papers in RGD have been used to annotate PALB2
  • Curation Notes: ClinVar Annotator: match by term: Fanconi anemia complementation group N
  • Original References(s): PMID:25741868 PMID:28492532 PMID:28580595 PMID:29263802 PMID:33811135


    • An association has been curated linking PALB2 and Fanconi anemia complementation group N in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • 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 by association of genotype and phenotype with RGD:11647823|RGD:28893742|RGD:28893745 (Homo sapiens) & RGD:11647823|RGD:28893742|RGD:28893745 (Homo sapiens) & RGD:11647823|RGD:28893742|RGD:28893745 (Homo sapiens)
  • 1 RGD objects have been annotated to Fanconi anemia complementation group N  (DOID:0111094)
  • 8 papers in RGD have been used to annotate PALB2
  • Curation Notes: ClinVar Annotator: match by term: Fanconi anemia complementation group N


    • An association has been curated linking PALB2 and Fanconi anemia complementation group N in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • 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 by association of genotype and phenotype with RGD:11090021|RGD:11091508|RGD:8697145 (Homo sapiens) & RGD:11090021|RGD:11091508|RGD:8697145 (Homo sapiens) & RGD:11090021|RGD:11091508|RGD:8697145 (Homo sapiens)
  • 1 RGD objects have been annotated to Fanconi anemia complementation group N  (DOID:0111094)
  • 8 papers in RGD have been used to annotate PALB2
  • Curation Notes: ClinVar Annotator: match by term: Fanconi anemia complementation group N
  • Original References(s): PMID:25741868 PMID:28492532 PMID:33471991


    • An association has been curated linking PALB2 and Fanconi anemia complementation group N in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • 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 by association of genotype and phenotype with RGD:11653601|RGD:13480117 (Homo sapiens) & RGD:11653601|RGD:13480117 (Homo sapiens)
  • 1 RGD objects have been annotated to Fanconi anemia complementation group N  (DOID:0111094)
  • 8 papers in RGD have been used to annotate PALB2
  • Curation Notes: ClinVar Annotator: match by term: Fanconi anemia complementation group N
  • Original References(s): PMID:28492532


    • An association has been curated linking PALB2 and Fanconi anemia complementation group N in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • 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 by association of genotype and phenotype with RGD:11347986 (Homo sapiens)
  • 1 RGD objects have been annotated to Fanconi anemia complementation group N  (DOID:0111094)
  • 8 papers in RGD have been used to annotate PALB2
  • Curation Notes: ClinVar Annotator: match by term: Fanconi anemia complementation group N
  • Original References(s): PMID:25085752 PMID:25741868 PMID:25980754 PMID:28492532 PMID:28873162 PMID:32885271 PMID:33471991 PMID:35610400


    • An association has been curated linking PALB2 and Fanconi anemia complementation group N in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • 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 by association of genotype and phenotype with RGD:11094820|RGD:150408664|RGD:150546347|RGD:401856314 (Homo sapiens) & RGD:11094820|RGD:150408664|RGD:150546347|RGD:401856314 (Homo sapiens) & RGD:11094820|RGD:150408664|RGD:150546347|RGD:401856314 (Homo sapiens) & RGD:11094820|RGD:150408664|RGD:150546347|RGD:401856314 (Homo sapiens)
  • 1 RGD objects have been annotated to Fanconi anemia complementation group N  (DOID:0111094)
  • 8 papers in RGD have been used to annotate PALB2
  • Curation Notes: ClinVar Annotator: match by term: Fanconi anemia complementation group N
  • Original References(s): PMID:25741868


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