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GENE - TERM ANNOTATION REPORT

48 Annotations Found.

An association has been curated linking Nod2 and Blau syndrome in Mus musculus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from van Duist MM, etal., Eur J Hum Genet. 2005 Jun;13(6):742-7.
  • The annotation has been inferred from sequence orthology with NOD2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 additional annotations were made from van Duist MM, etal., Eur J Hum Genet. 2005 Jun;13(6):742-7.
  • 1 RGD objects have been annotated to Blau syndrome  (DOID:0050678)
  • 67 papers in RGD have been used to annotate Nod2
  • Qualifier: susceptibility
  • Curation Notes: DNA:snp:cds:p.E383K (human)

  • This annotation was curated on 2015-12-12 12:00:34.0 by RGD . For more information contact us

    An association has been curated linking Nod2 and Blau syndrome in Mus musculus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from Rose CD, etal., Arthritis Rheum. 2009 Jun;60(6):1797-803. doi: 10.1002/art.24533.
  • The annotation has been inferred from sequence orthology with NOD2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 5 additional annotations were made from Rose CD, etal., Arthritis Rheum. 2009 Jun;60(6):1797-803. doi: 10.1002/art.24533.
  • 1 RGD objects have been annotated to Blau syndrome  (DOID:0050678)
  • 67 papers in RGD have been used to annotate Nod2
  • Qualifier: susceptibility
  • Curation Notes: DNA:snps:cds:p.R587C, p.C495Y, p.W490L (human)

  • This annotation was curated on 2015-12-12 12:00:34.0 by RGD . For more information contact us

    An association has been curated linking Nod2 and Blau syndrome in Mus musculus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from Miceli-Richard C, etal., Nat Genet. 2001 Sep;29(1):19-20.
  • The annotation has been inferred from sequence orthology with NOD2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 3 additional annotations were made from Miceli-Richard C, etal., Nat Genet. 2001 Sep;29(1):19-20.
  • 1 RGD objects have been annotated to Blau syndrome  (DOID:0050678)
  • 67 papers in RGD have been used to annotate Nod2
  • Qualifier: susceptibility
  • Curation Notes: DNA:snps:cds:p.R334Q, p.R334W, p.L469F (human)

  • This annotation was curated on 2015-12-12 12:00:34.0 by RGD . For more information contact us

    An association has been curated linking Nod2 and Blau syndrome in Mus musculus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from Okafuji I, etal., Arthritis Rheum. 2009 Jan;60(1):242-50. doi: 10.1002/art.24134.
  • The annotation has been inferred from sequence orthology with NOD2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 6 additional annotations were made from Okafuji I, etal., Arthritis Rheum. 2009 Jan;60(1):242-50. doi: 10.1002/art.24134.
  • 1 RGD objects have been annotated to Blau syndrome  (DOID:0050678)
  • 67 papers in RGD have been used to annotate Nod2
  • Qualifier: susceptibility
  • Curation Notes: DNA:snp:cds:p.E383G (human)

  • This annotation was curated on 2015-12-12 12:00:35.0 by RGD . For more information contact us

    An association has been curated linking Nod2 and Blau syndrome in Mus musculus.        

  • 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 NOD2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Blau syndrome  (DOID:0050678)
  • 67 papers in RGD have been used to annotate Nod2

  • This annotation was curated on 2019-10-09 19:57:09.0 by RGD . For more information contact us

    An association has been curated linking Nod2 and Blau syndrome 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 NOD2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Blau syndrome  (DOID:0050678)
  • 67 papers in RGD have been used to annotate Nod2
  • Curation Notes: ClinVar Annotator: match by term: Sarcoidosis, early-onset
  • Original References(s): PMID:11875755

  • This annotation was curated on 2019-10-08 13:07:16.0 by RGD . For more information contact us

    An association has been curated linking Nod2 and Blau syndrome 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 NOD2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Blau syndrome  (DOID:0050678)
  • 67 papers in RGD have been used to annotate Nod2
  • Curation Notes: ClinVar Annotator: match by OMIM:186580
  • Original References(s): PMID:11528384

  • This annotation was curated on 2019-10-08 13:06:28.0 by RGD . For more information contact us

    An association has been curated linking Nod2 and Blau syndrome 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 NOD2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Blau syndrome  (DOID:0050678)
  • 67 papers in RGD have been used to annotate Nod2
  • Curation Notes: ClinVar Annotator: match by term: Blau syndrome
  • Original References(s): PMID:28492532

  • This annotation was curated on 2019-10-08 13:10:16.0 by RGD . For more information contact us

    An association has been curated linking Nod2 and Blau syndrome 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 NOD2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Blau syndrome  (DOID:0050678)
  • 67 papers in RGD have been used to annotate Nod2
  • Curation Notes: ClinVar Annotator: match by term: Blau syndrome
  • Original References(s): PMID:11875755, PMID:28492532

  • This annotation was curated on 2019-10-08 13:07:35.0 by RGD . For more information contact us

    An association has been curated linking Nod2 and Blau syndrome in Mus musculus.        

  • 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 NOD2 (Homo sapiens) [(EXP) inferred from experiment]
  • 1 RGD objects have been annotated to Blau syndrome  (DOID:0050678)
  • 67 papers in RGD have been used to annotate Nod2
  • Curation Notes: CTD Direct Evidence: marker/mechanism
  • Original References(s): PMID:11528384, PMID:15086578, PMID:15459013, PMID:19467619

  • This annotation was curated on 2019-10-08 04:43:06.0 by RGD . For more information contact us

    An association has been curated linking Nod2 and Blau syndrome 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 NOD2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Blau syndrome  (DOID:0050678)
  • 67 papers in RGD have been used to annotate Nod2
  • Curation Notes: ClinVar Annotator: match by term: Blau syndrome
  • Original References(s): PMID:25741868, PMID:28492532

  • This annotation was curated on 2019-10-08 13:08:27.0 by RGD . For more information contact us

    An association has been curated linking Nod2 and Blau syndrome 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 NOD2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Blau syndrome  (DOID:0050678)
  • 67 papers in RGD have been used to annotate Nod2
  • Curation Notes: ClinVar Annotator: match by term: Blau syndrome
  • Original References(s): PMID:25741868

  • This annotation was curated on 2019-10-08 13:07:07.0 by RGD . For more information contact us

    An association has been curated linking Nod2 and Blau syndrome 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 NOD2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Blau syndrome  (DOID:0050678)
  • 67 papers in RGD have been used to annotate Nod2
  • Curation Notes: ClinVar Annotator: match by term: Sarcoidosis, early-onset
  • Original References(s): PMID:15459013

  • This annotation was curated on 2019-10-08 13:05:57.0 by RGD . For more information contact us

    An association has been curated linking Nod2 and Blau syndrome 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 NOD2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Blau syndrome  (DOID:0050678)
  • 67 papers in RGD have been used to annotate Nod2
  • Curation Notes: ClinVar Annotator: match by OMIM:186580

  • This annotation was curated on 2019-10-08 13:10:24.0 by RGD . For more information contact us

    An association has been curated linking Nod2 and Blau syndrome 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 NOD2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Blau syndrome  (DOID:0050678)
  • 67 papers in RGD have been used to annotate Nod2
  • Curation Notes: ClinVar Annotator: match by term: Blau syndrome
  • Original References(s): PMID:11875755, PMID:17941079, PMID:28492532

  • This annotation was curated on 2019-10-08 13:07:23.0 by RGD . For more information contact us

    An association has been curated linking Nod2 and Blau syndrome 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 NOD2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Blau syndrome  (DOID:0050678)
  • 67 papers in RGD have been used to annotate Nod2
  • Curation Notes: ClinVar Annotator: match by OMIM:186580
  • Original References(s): PMID:11385576, PMID:11875755, PMID:12626759, PMID:15459013

  • This annotation was curated on 2019-10-08 13:05:57.0 by RGD . For more information contact us

    An association has been curated linking Nod2 and Blau syndrome 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 NOD2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Blau syndrome  (DOID:0050678)
  • 67 papers in RGD have been used to annotate Nod2
  • Curation Notes: ClinVar Annotator: match by term: Blau syndrome
  • Original References(s): PMID:24033266

  • This annotation was curated on 2019-10-08 13:09:03.0 by RGD . For more information contact us

    An association has been curated linking Nod2 and Blau syndrome 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 NOD2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Blau syndrome  (DOID:0050678)
  • 67 papers in RGD have been used to annotate Nod2
  • Curation Notes: ClinVar Annotator: match by term: Blau syndrome
  • Original References(s): PMID:18507017, PMID:20230816, PMID:24033266

  • This annotation was curated on 2019-10-08 13:09:35.0 by RGD . For more information contact us

    An association has been curated linking Nod2 and Blau syndrome 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 NOD2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Blau syndrome  (DOID:0050678)
  • 67 papers in RGD have been used to annotate Nod2
  • Curation Notes: ClinVar Annotator: match by term: Blau syndrome
  • Original References(s): PMID:11385576, PMID:11875755, PMID:12626759, PMID:15024686, PMID:24960071, PMID:28492532

  • This annotation was curated on 2019-10-08 13:07:16.0 by RGD . For more information contact us

    An association has been curated linking Nod2 and Blau syndrome 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 NOD2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Blau syndrome  (DOID:0050678)
  • 67 papers in RGD have been used to annotate Nod2
  • Curation Notes: ClinVar Annotator: match by term: Blau syndrome
  • Original References(s): PMID:11528384, PMID:14522785, PMID:15044951, PMID:15086578, PMID:15459013, PMID:17157607, PMID:18955195, PMID:22509093, PMID:24713464, PMID:25416713, PMID:28492532, PMID:9124059

  • This annotation was curated on 2019-10-08 13:06:28.0 by RGD . For more information contact us

    An association has been curated linking Nod2 and Blau syndrome 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 NOD2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Blau syndrome  (DOID:0050678)
  • 67 papers in RGD have been used to annotate Nod2
  • Curation Notes: ClinVar Annotator: match by term: Blau syndrome
  • Original References(s): PMID:11385576, PMID:28492532

  • This annotation was curated on 2019-10-08 13:05:35.0 by RGD . For more information contact us

    An association has been curated linking Nod2 and Blau syndrome 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 NOD2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Blau syndrome  (DOID:0050678)
  • 67 papers in RGD have been used to annotate Nod2
  • Curation Notes: ClinVar Annotator: match by term: Blau syndrome
  • Original References(s): PMID:11385576, PMID:11875755, PMID:12019468, PMID:12512038, PMID:15024686, PMID:15198989, PMID:15571588, PMID:15770725, PMID:15967635, PMID:18240302, PMID:18489434, PMID:18541930, PMID:19713276, PMID:20959815, PMID:21274544, PMID:21548950, PMID:21830272, PMID:21914217, PMID:22684479, PMID:23102769, PMID:24033266, PMID:26070941, PMID:28492532

  • This annotation was curated on 2019-10-08 13:06:28.0 by RGD . For more information contact us

    An association has been curated linking Nod2 and Blau syndrome 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 NOD2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Blau syndrome  (DOID:0050678)
  • 67 papers in RGD have been used to annotate Nod2
  • Curation Notes: ClinVar Annotator: match by term: Blau syndrome
  • Original References(s): PMID:11087742, PMID:28492532

  • This annotation was curated on 2019-10-08 13:06:20.0 by RGD . For more information contact us

    An association has been curated linking Nod2 and Blau syndrome 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 NOD2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Blau syndrome  (DOID:0050678)
  • 67 papers in RGD have been used to annotate Nod2
  • Curation Notes: ClinVar Annotator: match by term: Blau syndrome
  • Original References(s): PMID:27306066, PMID:28492532

  • This annotation was curated on 2019-10-08 13:04:59.0 by RGD . For more information contact us

    An association has been curated linking Nod2 and Blau syndrome 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 NOD2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Blau syndrome  (DOID:0050678)
  • 67 papers in RGD have been used to annotate Nod2
  • Curation Notes: ClinVar Annotator: match by term: Blau syndrome
  • Original References(s): PMID:15024686, PMID:21983784, PMID:28492532

  • This annotation was curated on 2019-10-08 13:05:34.0 by RGD . For more information contact us

    An association has been curated linking Nod2 and Blau syndrome 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 NOD2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Blau syndrome  (DOID:0050678)
  • 67 papers in RGD have been used to annotate Nod2
  • Curation Notes: ClinVar Annotator: match by term: Blau syndrome
  • Original References(s): PMID:15812565, PMID:18718560, PMID:19479836, PMID:20565245, PMID:25093298, PMID:25136265, PMID:25829188, PMID:27339507, PMID:28492532

  • This annotation was curated on 2019-10-08 13:06:29.0 by RGD . For more information contact us

    An association has been curated linking Nod2 and Blau syndrome 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 NOD2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Blau syndrome  (DOID:0050678)
  • 67 papers in RGD have been used to annotate Nod2
  • Curation Notes: ClinVar Annotator: match by term: Blau syndrome
  • Original References(s): PMID:11385576, PMID:11385577, PMID:11425413, PMID:11910337, PMID:12019468, PMID:12512038, PMID:15024686, PMID:15190267, PMID:15198989, PMID:15571588, PMID:18240302, PMID:18489434, PMID:19713276, PMID:21335489, PMID:21548950, PMID:22684479, PMID:26500656, PMID:28492532

  • This annotation was curated on 2019-10-08 13:06:28.0 by RGD . For more information contact us

    An association has been curated linking Nod2 and Blau syndrome 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 NOD2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Blau syndrome  (DOID:0050678)
  • 67 papers in RGD have been used to annotate Nod2
  • Curation Notes: ClinVar Annotator: match by term: Blau syndrome
  • Original References(s): PMID:11875755, PMID:16278823, PMID:28492532

  • This annotation was curated on 2019-10-08 13:05:35.0 by RGD . For more information contact us

    An association has been curated linking Nod2 and Blau syndrome 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 NOD2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Blau syndrome  (DOID:0050678)
  • 67 papers in RGD have been used to annotate Nod2
  • Curation Notes: ClinVar Annotator: match by term: Blau syndrome
  • Original References(s): PMID:12115249, PMID:28492532

  • This annotation was curated on 2019-10-08 13:05:34.0 by RGD . For more information contact us

    An association has been curated linking Nod2 and Blau syndrome 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 NOD2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Blau syndrome  (DOID:0050678)
  • 67 papers in RGD have been used to annotate Nod2
  • Curation Notes: ClinVar Annotator: match by term: Blau syndrome
  • Original References(s): PMID:11875755, PMID:15459013, PMID:7825454

  • This annotation was curated on 2019-10-08 13:05:57.0 by RGD . For more information contact us

    An association has been curated linking Nod2 and Blau syndrome 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 NOD2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Blau syndrome  (DOID:0050678)
  • 67 papers in RGD have been used to annotate Nod2
  • Curation Notes: ClinVar Annotator: match by term: Blau syndrome
  • Original References(s): PMID:11385576, PMID:11875755, PMID:12115249, PMID:12626759, PMID:28492532

  • This annotation was curated on 2019-10-08 13:07:15.0 by RGD . For more information contact us

    An association has been curated linking Nod2 and Blau syndrome 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 NOD2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Blau syndrome  (DOID:0050678)
  • 67 papers in RGD have been used to annotate Nod2
  • Curation Notes: ClinVar Annotator: match by term: Blau syndrome
  • Original References(s): PMID:11875755, PMID:12626759, PMID:26500656, PMID:28492532

  • This annotation was curated on 2019-10-08 13:05:35.0 by RGD . For more information contact us

    An association has been curated linking Nod2 and Blau syndrome 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 NOD2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Blau syndrome  (DOID:0050678)
  • 67 papers in RGD have been used to annotate Nod2
  • Curation Notes: ClinVar Annotator: match by term: Blau syndrome
  • Original References(s): PMID:11528384, PMID:28492532

  • This annotation was curated on 2019-10-08 13:06:28.0 by RGD . For more information contact us

    An association has been curated linking Nod2 and Blau syndrome 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 NOD2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Blau syndrome  (DOID:0050678)
  • 67 papers in RGD have been used to annotate Nod2
  • Curation Notes: ClinVar Annotator: match by term: Blau syndrome
  • Original References(s): PMID:24876985, PMID:28492532

  • This annotation was curated on 2019-10-08 13:04:47.0 by RGD . For more information contact us

    An association has been curated linking Nod2 and Blau syndrome 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 NOD2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Blau syndrome  (DOID:0050678)
  • 67 papers in RGD have been used to annotate Nod2
  • Curation Notes: ClinVar Annotator: match by term: Blau syndrome
  • Original References(s): PMID:15024686, PMID:28492532

  • This annotation was curated on 2019-10-08 13:07:16.0 by RGD . For more information contact us

    An association has been curated linking Nod2 and Blau syndrome 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 NOD2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Blau syndrome  (DOID:0050678)
  • 67 papers in RGD have been used to annotate Nod2
  • Curation Notes: ClinVar Annotator: match by term: Blau syndrome
  • Original References(s): PMID:12577202, PMID:14765395, PMID:15024686, PMID:19467619, PMID:21914217, PMID:23102769, PMID:26070941

  • This annotation was curated on 2019-10-08 13:06:28.0 by RGD . For more information contact us

    An association has been curated linking Nod2 and Blau syndrome 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 NOD2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Blau syndrome  (DOID:0050678)
  • 67 papers in RGD have been used to annotate Nod2
  • Curation Notes: ClinVar Annotator: match by term: Blau syndrome
  • Original References(s): PMID:11385576, PMID:11385577, PMID:12019468, PMID:12512038, PMID:12557156, PMID:15024686, PMID:15190267, PMID:15198989, PMID:15571588, PMID:18489434, PMID:19713276, PMID:21548950, PMID:21830272, PMID:26070941, PMID:28492532

  • This annotation was curated on 2019-10-08 13:06:28.0 by RGD . For more information contact us

    An association has been curated linking Nod2 and Blau syndrome 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 NOD2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Blau syndrome  (DOID:0050678)
  • 67 papers in RGD have been used to annotate Nod2
  • Curation Notes: ClinVar Annotator: match by term: Blau syndrome
  • Original References(s): PMID:11875755, PMID:12626759, PMID:21983784, PMID:22942351, PMID:28492532

  • This annotation was curated on 2019-10-08 13:09:34.0 by RGD . For more information contact us

    An association has been curated linking Nod2 and Blau syndrome 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 NOD2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Blau syndrome  (DOID:0050678)
  • 67 papers in RGD have been used to annotate Nod2
  • Curation Notes: ClinVar Annotator: match by term: Blau syndrome
  • Original References(s): PMID:11385576, PMID:17698784, PMID:25741868

  • This annotation was curated on 2019-10-08 13:05:35.0 by RGD . For more information contact us

    An association has been curated linking Nod2 and Blau syndrome 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 NOD2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Blau syndrome  (DOID:0050678)
  • 67 papers in RGD have been used to annotate Nod2
  • Curation Notes: ClinVar Annotator: match by term: Blau syndrome
  • Original References(s): PMID:11385576, PMID:11875755, PMID:12626759, PMID:21983784, PMID:25741868

  • This annotation was curated on 2019-10-08 13:05:35.0 by RGD . For more information contact us

    An association has been curated linking Nod2 and Blau syndrome 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 NOD2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Blau syndrome  (DOID:0050678)
  • 67 papers in RGD have been used to annotate Nod2
  • Curation Notes: ClinVar Annotator: match by term: Blau syndrome
  • Original References(s): PMID:11385576, PMID:11875755, PMID:12626759, PMID:14508222, PMID:15044951, PMID:15770725, PMID:25741868, PMID:28492532

  • This annotation was curated on 2019-10-08 13:07:16.0 by RGD . For more information contact us

    An association has been curated linking Nod2 and Blau syndrome 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 NOD2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Blau syndrome  (DOID:0050678)
  • 67 papers in RGD have been used to annotate Nod2
  • Curation Notes: ClinVar Annotator: match by term: Blau syndrome
  • Original References(s): PMID:15459013, PMID:28492532

  • This annotation was curated on 2019-10-08 13:07:16.0 by RGD . For more information contact us

    An association has been curated linking Nod2 and Blau syndrome 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 NOD2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Blau syndrome  (DOID:0050678)
  • 67 papers in RGD have been used to annotate Nod2
  • Curation Notes: ClinVar Annotator: match by term: Blau syndrome
  • Original References(s): PMID:15044951, PMID:28492532

  • This annotation was curated on 2019-10-08 13:05:02.0 by RGD . For more information contact us

    An association has been curated linking Nod2 and Blau syndrome 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 NOD2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Blau syndrome  (DOID:0050678)
  • 67 papers in RGD have been used to annotate Nod2
  • Curation Notes: ClinVar Annotator: match by term: Blau syndrome
  • Original References(s): PMID:17941079, PMID:28492532

  • This annotation was curated on 2019-10-08 13:07:16.0 by RGD . For more information contact us

    An association has been curated linking Nod2 and Blau syndrome 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 NOD2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Blau syndrome  (DOID:0050678)
  • 67 papers in RGD have been used to annotate Nod2
  • Curation Notes: ClinVar Annotator: match by term: Blau syndrome
  • Original References(s): PMID:16485124, PMID:28492532

  • This annotation was curated on 2019-10-08 13:05:34.0 by RGD . For more information contact us

    An association has been curated linking Nod2 and Blau syndrome 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 NOD2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Blau syndrome  (DOID:0050678)
  • 67 papers in RGD have been used to annotate Nod2
  • Curation Notes: ClinVar Annotator: match by term: Blau syndrome
  • Original References(s): PMID:11385576, PMID:11875755, PMID:12626759, PMID:28492532

  • This annotation was curated on 2019-10-08 13:05:35.0 by RGD . For more information contact us

    An association has been curated linking Nod2 and Blau syndrome 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 NOD2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Blau syndrome  (DOID:0050678)
  • 67 papers in RGD have been used to annotate Nod2
  • Curation Notes: ClinVar Annotator: match by term: Blau syndrome
  • Original References(s): PMID:23334666, PMID:28492532

  • This annotation was curated on 2019-10-08 13:08:20.0 by RGD . For more information contact us

    An association has been curated linking Nod2 and Blau syndrome 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 NOD2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Blau syndrome  (DOID:0050678)
  • 67 papers in RGD have been used to annotate Nod2
  • Curation Notes: ClinVar Annotator: match by term: Blau syndrome
  • Original References(s): PMID:11385576, PMID:11875755, PMID:12115249, PMID:15044951, PMID:28492532

  • This annotation was curated on 2019-10-08 13:05:35.0 by RGD . For more information contact us

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