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GENE - TERM ANNOTATION REPORT

2 Annotations Found.

An association has been curated linking Phox2b and Hereditary Neoplastic Syndromes in Mus musculus.        

  • 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 PHOX2B (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1283 RGD objects have been annotated to Hereditary Neoplastic Syndromes  (DOID:9007071)
  • 14 papers in RGD have been used to annotate Phox2b
  • Curation Notes: ClinVar Annotator: match by term: Hereditary Cancer Syndrome | ClinVar Annotator: match by term: Hereditary cancer-predisposing syndrome | ClinVar Annotator: match by term: Hereditary neoplastic syndrome | ClinVar Annotator: match by term: Neoplastic Syndromes, Hereditary
  • Original References(s): PMID:11953745 PMID:12438263 PMID:12631670 PMID:12640453 PMID:14566559 PMID:14608649 PMID:14709596 PMID:15024693 PMID:15121777 PMID:15334515 PMID:15338462 PMID:15657873 PMID:15949893 PMID:16249188 PMID:16443855 PMID:16691592 PMID:16763219 PMID:16830328 PMID:16888290 PMID:17576681 PMID:17637745 PMID:17765533 PMID:18079495 PMID:18157832 PMID:18292934 PMID:18407552 PMID:18798833 PMID:19011468 PMID:19058226 PMID:19422034 PMID:20089899 PMID:20208042 PMID:20301600 PMID:20456320 PMID:21373876 PMID:23460419 PMID:23622117 PMID:23754957 PMID:23873030 PMID:24033266 PMID:24169930 PMID:24728327 PMID:25156769 PMID:25319843 PMID:25741868 PMID:26063465 PMID:26375764 PMID:26580448 PMID:27013732 PMID:27153395 PMID:28371199 PMID:28422456 PMID:28433712 PMID:28492532 PMID:28873162 PMID:29531718 PMID:29543228 PMID:29641532 PMID:29704303 PMID:30518452 PMID:30672101 PMID:30850150 PMID:32573669 PMID:33958749 PMID:34298581 PMID:9536098


    • An association has been curated linking Phox2b and Hereditary Neoplastic Syndromes in Mus musculus.        

  • 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 PHOX2B (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1283 RGD objects have been annotated to Hereditary Neoplastic Syndromes  (DOID:9007071)
  • 14 papers in RGD have been used to annotate Phox2b
  • Curation Notes: ClinVar Annotator: match by term: Hereditary Cancer Syndrome | ClinVar Annotator: match by term: Hereditary cancer-predisposing syndrome | ClinVar Annotator: match by term: Hereditary neoplastic syndrome | ClinVar Annotator: match by term: Neoplastic Syndromes, Hereditary
  • Original References(s): PMID:11953745 PMID:12438263 PMID:12631670 PMID:12640453 PMID:14566559 PMID:14608649 PMID:14709596 PMID:15024693 PMID:15121777 PMID:15334515 PMID:15338462 PMID:15657873 PMID:15949893 PMID:16199547 PMID:16249188 PMID:16691592 PMID:16763219 PMID:16830328 PMID:16888290 PMID:17576681 PMID:17637745 PMID:17765533 PMID:18079495 PMID:18157832 PMID:18292934 PMID:18407552 PMID:18798833 PMID:19011468 PMID:19058226 PMID:19422034 PMID:20089899 PMID:20208042 PMID:20301600 PMID:20456320 PMID:21373876 PMID:23460419 PMID:23622117 PMID:23754957 PMID:23873030 PMID:24033266 PMID:24169930 PMID:24728327 PMID:25156769 PMID:25319843 PMID:25741868 PMID:26063465 PMID:26375764 PMID:26580448 PMID:27013732 PMID:27153395 PMID:28371199 PMID:28422456 PMID:28433712 PMID:28492532 PMID:28873162 PMID:29531718 PMID:29543228 PMID:29641532 PMID:29704303 PMID:30518452 PMID:30672101 PMID:30850150 PMID:32573669 PMID:33958749 PMID:34012823 PMID:34298581 PMID:9536098


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