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GENE - TERM ANNOTATION REPORT

7 Annotations Found.

An association has been curated linking F11 and factor XI deficiency in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
    		•  
  • The annotation was made from Ventura C, etal., Thromb Haemost. 2000 Nov;84(5):833-40.
  • The annotation has been inferred from sequence orthology with F11 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 additional annotations were made from Ventura C, etal., Thromb Haemost. 2000 Nov;84(5):833-40.
  • 11 RGD objects have been annotated to factor XI deficiency  (DOID:2229)
  • 21 papers in RGD have been used to annotate F11
  • Curation Notes: DNA:missense, nonsense, duplication, deletion:cds:


    • An association has been curated linking F11 and factor XI deficiency in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
    		•  
  • The annotation was made from Asakai R, etal., Proc Natl Acad Sci U S A. 1989 Oct;86(20):7667-71.
  • The annotation has been inferred from sequence orthology with F11 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 additional annotations were made from Asakai R, etal., Proc Natl Acad Sci U S A. 1989 Oct;86(20):7667-71.
  • 11 RGD objects have been annotated to factor XI deficiency  (DOID:2229)
  • 21 papers in RGD have been used to annotate F11


    • An association has been curated linking F11 and factor XI deficiency in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
    		•  
  • The annotation was made from Sato E, etal., Am J Hematol. 2000 Apr;63(4):165-9.
  • The annotation has been inferred from sequence orthology with F11 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 3 additional annotations were made from Sato E, etal., Am J Hematol. 2000 Apr;63(4):165-9.
  • 11 RGD objects have been annotated to factor XI deficiency  (DOID:2229)
  • 21 papers in RGD have been used to annotate F11
  • Curation Notes: DNA:nonsense mutation:exon:G263X(human)


    • An association has been curated linking F11 and factor XI deficiency 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 F11 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 11 RGD objects have been annotated to factor XI deficiency  (DOID:2229)
  • 21 papers in RGD have been used to annotate F11


    • An association has been curated linking F11 and factor XI deficiency in Rattus norvegicus.        

  • The association was inferred from sequence or structural similarity (ISS)
    		•  
  • The annotation was made from RGD automated import pipeline for MGI gene-to-disease annotations
  • The annotation has been inferred from sequence or structural similarity with F11 (Mus musculus) [(IAGP) inferred by association of genotype and phenotype]
  • 11 RGD objects have been annotated to factor XI deficiency  (DOID:2229)
  • 21 papers in RGD have been used to annotate F11
  • Curation Notes: OMIM:612416


    • An association has been curated linking F11 and factor XI deficiency in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
    		•  
  • The annotation was made from RGD automated import pipeline for CTD gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with F11 (Homo sapiens) [(EXP) inferred from experiment]
  • 11 RGD objects have been annotated to factor XI deficiency  (DOID:2229)
  • 21 papers in RGD have been used to annotate F11
  • Curation Notes: CTD Direct Evidence: marker/mechanism


    • An association has been curated linking F11 and factor XI deficiency 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 F11 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 11 RGD objects have been annotated to factor XI deficiency  (DOID:2229)
  • 21 papers in RGD have been used to annotate F11
  • Curation Notes: ClinVar Annotator: match by term: Hereditary factor XI deficiency disease | ClinVar Annotator: match by term: Plasma factor XI deficiency
  • Original References(s): PMID:10444286 PMID:10593931 PMID:10606881 PMID:10706758 PMID:11122101 PMID:11127865 PMID:11418471 PMID:11895778 PMID:12586617 PMID:12716376 PMID:12879434 PMID:14508802 PMID:14717969 PMID:15026311 PMID:15090552 PMID:15140127 PMID:15140147 PMID:15180874 PMID:15456490 PMID:1547342 PMID:15531455 PMID:15613027 PMID:15634276 PMID:15728123 PMID:15749683 PMID:15842381 PMID:15870541 PMID:15946525 PMID:15953011 PMID:15968392 PMID:16079124 PMID:16086308 PMID:16199547 PMID:16519703 PMID:16607084 PMID:16787881 PMID:16835901 PMID:17229051 PMID:17549289 PMID:17576681 PMID:18005151 PMID:18024374 PMID:18327400 PMID:18388506 PMID:18446632 PMID:18515884 PMID:18758779 PMID:18832909 PMID:18839438 PMID:19367158 PMID:19652879 PMID:20015217 PMID:20398070 PMID:2052060 PMID:20523169 PMID:21192253 PMID:21457405 PMID:21649796 PMID:21668437 PMID:21718436 PMID:21824284 PMID:22016685 PMID:22159456 PMID:22197449 PMID:23305485 PMID:23315997 PMID:23332144 PMID:23929304 PMID:24033266 PMID:24112640 PMID:24982842 PMID:25074526 PMID:25158988 PMID:25681615 PMID:25741868 PMID:25741869 PMID:26558335 PMID:26879396 PMID:27067486 PMID:27710856 PMID:27723456 PMID:2813350 PMID:28445521 PMID:28492532 PMID:28615222 PMID:28960694 PMID:29138690 PMID:29178608 PMID:29367083 PMID:30261521 PMID:31064749 PMID:31644447 PMID:32220196 PMID:32333264 PMID:32581362 PMID:32596782 PMID:33751533 PMID:34355501 PMID:34776502 PMID:35059554 PMID:35627175 PMID:36195107 PMID:7669672 PMID:7888672 PMID:8832909 PMID:9326232 PMID:9401068 PMID:9536098 PMID:9787168


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