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GENE - TERM ANNOTATION REPORT

64 Annotations Found.

An association has been curated linking Palb2 and Fanconi anemia complementation group N in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with PALB2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Fanconi anemia complementation group N  (DOID:0111094)
  • 7 papers in RGD have been used to annotate Palb2
  • Curation Notes: ClinVar Annotator: match by OMIM:610832
  • Original References(s): PMID:17200671, PMID:19264984


  • An association has been curated linking Palb2 and Fanconi anemia complementation group N in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from OMIM Disease Annotation Pipeline
  • The annotation has been inferred from sequence orthology with PALB2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Fanconi anemia complementation group N  (DOID:0111094)
  • 7 papers in RGD have been used to annotate Palb2


  • An association has been curated linking Palb2 and Fanconi anemia complementation group N in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with PALB2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Fanconi anemia complementation group N  (DOID:0111094)
  • 7 papers in RGD have been used to annotate Palb2
  • Curation Notes: ClinVar Annotator: match by OMIM:610832


  • An association has been curated linking Palb2 and Fanconi anemia complementation group N in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with PALB2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Fanconi anemia complementation group N  (DOID:0111094)
  • 7 papers in RGD have been used to annotate Palb2
  • Curation Notes: ClinVar Annotator: match by OMIM:610832
  • Original References(s): PMID:17200672


  • An association has been curated linking Palb2 and Fanconi anemia complementation group N in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with PALB2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Fanconi anemia complementation group N  (DOID:0111094)
  • 7 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:18302019, PMID:19264984, PMID:20412113, PMID:25099575, PMID:25452441, PMID:25741868, PMID:26283626, PMID:26845104, PMID:28492532, PMID:29909963


  • An association has been curated linking Palb2 and Fanconi anemia complementation group N in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with PALB2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Fanconi anemia complementation group N  (DOID:0111094)
  • 7 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, PMID:17924555, PMID:19264984, PMID:21285249, PMID:23935836, PMID:25099575, PMID:25525159, PMID:25741868, PMID:28319063, PMID:28492532


  • An association has been curated linking Palb2 and Fanconi anemia complementation group N in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with PALB2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Fanconi anemia complementation group N  (DOID:0111094)
  • 7 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:25452441, PMID:25741868, PMID:26283626, PMID:26315354, PMID:26681312, PMID:26845104, PMID:26898890, PMID:27356891, PMID:28008555, PMID:28492532, PMID:29360161


  • An association has been curated linking Palb2 and Fanconi anemia complementation group N in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with PALB2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Fanconi anemia complementation group N  (DOID:0111094)
  • 7 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 Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with PALB2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Fanconi anemia complementation group N  (DOID:0111094)
  • 7 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:25186627, PMID:25503501, PMID:25741868, PMID:25980754, PMID:26283626, PMID:26467025, PMID:27153395, PMID:28492532, PMID:31586400


  • An association has been curated linking Palb2 and Fanconi anemia complementation group N in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with PALB2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Fanconi anemia complementation group N  (DOID:0111094)
  • 7 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:19584259, PMID:19609323, PMID:21165770, PMID:23341105, PMID:25099575, PMID:25452441, PMID:25741868, PMID:26467025, PMID:26845104, PMID:28281021, PMID:28492532


  • An association has been curated linking Palb2 and Fanconi anemia complementation group N in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with PALB2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Fanconi anemia complementation group N  (DOID:0111094)
  • 7 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, PMID:28492532


  • An association has been curated linking Palb2 and Fanconi anemia complementation group N in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with PALB2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Fanconi anemia complementation group N  (DOID:0111094)
  • 7 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: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:28492532


  • An association has been curated linking Palb2 and Fanconi anemia complementation group N in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with PALB2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Fanconi anemia complementation group N  (DOID:0111094)
  • 7 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


  • An association has been curated linking Palb2 and Fanconi anemia complementation group N in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with PALB2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Fanconi anemia complementation group N  (DOID:0111094)
  • 7 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: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:30287823


  • An association has been curated linking Palb2 and Fanconi anemia complementation group N in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with PALB2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Fanconi anemia complementation group N  (DOID:0111094)
  • 7 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


  • An association has been curated linking Palb2 and Fanconi anemia complementation group N in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with PALB2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Fanconi anemia complementation group N  (DOID:0111094)
  • 7 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 Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with PALB2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Fanconi anemia complementation group N  (DOID:0111094)
  • 7 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:25741868, PMID:26283626, PMID:28492532


  • An association has been curated linking Palb2 and Fanconi anemia complementation group N in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with PALB2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Fanconi anemia complementation group N  (DOID:0111094)
  • 7 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 Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with PALB2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Fanconi anemia complementation group N  (DOID:0111094)
  • 7 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


  • An association has been curated linking Palb2 and Fanconi anemia complementation group N in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with PALB2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Fanconi anemia complementation group N  (DOID:0111094)
  • 7 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:25356972, PMID:25741868, PMID:25980754, PMID:26283626, PMID:26315354, PMID:26467025, PMID:28051113, PMID:28492532, PMID:29052111


  • An association has been curated linking Palb2 and Fanconi anemia complementation group N in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with PALB2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Fanconi anemia complementation group N  (DOID:0111094)
  • 7 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:25741868, PMID:26315354, PMID:26467025, PMID:28492532, PMID:30287823


  • An association has been curated linking Palb2 and Fanconi anemia complementation group N in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with PALB2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Fanconi anemia complementation group N  (DOID:0111094)
  • 7 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 Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with PALB2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Fanconi anemia complementation group N  (DOID:0111094)
  • 7 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:25356972, PMID:25741868, PMID:26467025, PMID:28492532


  • An association has been curated linking Palb2 and Fanconi anemia complementation group N in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with PALB2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Fanconi anemia complementation group N  (DOID:0111094)
  • 7 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 Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with PALB2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Fanconi anemia complementation group N  (DOID:0111094)
  • 7 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 Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with PALB2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Fanconi anemia complementation group N  (DOID:0111094)
  • 7 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 Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with PALB2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Fanconi anemia complementation group N  (DOID:0111094)
  • 7 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 Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with PALB2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Fanconi anemia complementation group N  (DOID:0111094)
  • 7 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 Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with PALB2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Fanconi anemia complementation group N  (DOID:0111094)
  • 7 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 Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with PALB2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Fanconi anemia complementation group N  (DOID:0111094)
  • 7 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 Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with PALB2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Fanconi anemia complementation group N  (DOID:0111094)
  • 7 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 Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with PALB2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Fanconi anemia complementation group N  (DOID:0111094)
  • 7 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


  • An association has been curated linking Palb2 and Fanconi anemia complementation group N in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with PALB2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Fanconi anemia complementation group N  (DOID:0111094)
  • 7 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:25741868, PMID:26283626, PMID:26467025, PMID:28492532


  • An association has been curated linking Palb2 and Fanconi anemia complementation group N in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with PALB2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Fanconi anemia complementation group N  (DOID:0111094)
  • 7 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 Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with PALB2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Fanconi anemia complementation group N  (DOID:0111094)
  • 7 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


  • An association has been curated linking Palb2 and Fanconi anemia complementation group N in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with PALB2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Fanconi anemia complementation group N  (DOID:0111094)
  • 7 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 Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with PALB2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Fanconi anemia complementation group N  (DOID:0111094)
  • 7 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 Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with PALB2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Fanconi anemia complementation group N  (DOID:0111094)
  • 7 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


  • An association has been curated linking Palb2 and Fanconi anemia complementation group N in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with PALB2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Fanconi anemia complementation group N  (DOID:0111094)
  • 7 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 Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with PALB2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Fanconi anemia complementation group N  (DOID:0111094)
  • 7 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:28492532


  • An association has been curated linking Palb2 and Fanconi anemia complementation group N in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with PALB2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Fanconi anemia complementation group N  (DOID:0111094)
  • 7 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 Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with PALB2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Fanconi anemia complementation group N  (DOID:0111094)
  • 7 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 Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with PALB2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Fanconi anemia complementation group N  (DOID:0111094)
  • 7 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


  • An association has been curated linking Palb2 and Fanconi anemia complementation group N in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with PALB2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Fanconi anemia complementation group N  (DOID:0111094)
  • 7 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 Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with PALB2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Fanconi anemia complementation group N  (DOID:0111094)
  • 7 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 Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with PALB2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Fanconi anemia complementation group N  (DOID:0111094)
  • 7 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:30287823


  • An association has been curated linking Palb2 and Fanconi anemia complementation group N in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with PALB2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Fanconi anemia complementation group N  (DOID:0111094)
  • 7 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 Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with PALB2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Fanconi anemia complementation group N  (DOID:0111094)
  • 7 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:25980754, PMID:28492532, PMID:28873162


  • An association has been curated linking Palb2 and Fanconi anemia complementation group N in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with PALB2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Fanconi anemia complementation group N  (DOID:0111094)
  • 7 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 Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with PALB2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Fanconi anemia complementation group N  (DOID:0111094)
  • 7 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 Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with PALB2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Fanconi anemia complementation group N  (DOID:0111094)
  • 7 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


  • An association has been curated linking Palb2 and Fanconi anemia complementation group N in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with PALB2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Fanconi anemia complementation group N  (DOID:0111094)
  • 7 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:28492532


  • An association has been curated linking Palb2 and Fanconi anemia complementation group N in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with PALB2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Fanconi anemia complementation group N  (DOID:0111094)
  • 7 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


  • An association has been curated linking Palb2 and Fanconi anemia complementation group N in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with PALB2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Fanconi anemia complementation group N  (DOID:0111094)
  • 7 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:28492532, PMID:30287823


  • An association has been curated linking Palb2 and Fanconi anemia complementation group N in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with PALB2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Fanconi anemia complementation group N  (DOID:0111094)
  • 7 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


  • An association has been curated linking Palb2 and Fanconi anemia complementation group N in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with PALB2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Fanconi anemia complementation group N  (DOID:0111094)
  • 7 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


  • An association has been curated linking Palb2 and Fanconi anemia complementation group N in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with PALB2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Fanconi anemia complementation group N  (DOID:0111094)
  • 7 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, PMID:21365267, PMID:21618343, PMID:25525159, PMID:25741868, PMID:28152038, PMID:28492532, PMID:28779002


  • An association has been curated linking Palb2 and Fanconi anemia complementation group N in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with PALB2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Fanconi anemia complementation group N  (DOID:0111094)
  • 7 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


  • An association has been curated linking Palb2 and Fanconi anemia complementation group N in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with PALB2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Fanconi anemia complementation group N  (DOID:0111094)
  • 7 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:28796317, PMID:30287823, PMID:32566746


  • An association has been curated linking Palb2 and Fanconi anemia complementation group N in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with PALB2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Fanconi anemia complementation group N  (DOID:0111094)
  • 7 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:26689913, PMID:27621404, PMID:28492532, PMID:28796317, PMID:29667044, PMID:29802286, PMID:30287823, PMID:32566746


  • An association has been curated linking Palb2 and Fanconi anemia complementation group N in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with PALB2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Fanconi anemia complementation group N  (DOID:0111094)
  • 7 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 Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with PALB2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Fanconi anemia complementation group N  (DOID:0111094)
  • 7 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:32566746


  • An association has been curated linking Palb2 and Fanconi anemia complementation group N in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with PALB2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Fanconi anemia complementation group N  (DOID:0111094)
  • 7 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 Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with PALB2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Fanconi anemia complementation group N  (DOID:0111094)
  • 7 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:27783279, PMID:28380452, PMID:28492532, PMID:28796317, PMID:29190888, PMID:30287823, PMID:32566746


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    RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.