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GENE - TERM ANNOTATION REPORT

27 Annotations Found.

An association has been curated linking NBAS and Infantile Liver Failure Syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from OMIM Disease Annotation Pipeline
  • 1 RGD objects have been annotated to Infantile Liver Failure Syndrome 2  (DOID:9007272)
  • 5 papers in RGD have been used to annotate NBAS


    • An association has been curated linking NBAS and Infantile Liver Failure Syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:10056670 (Homo sapiens)
  • 1 RGD objects have been annotated to Infantile Liver Failure Syndrome 2  (DOID:9007272)
  • 5 papers in RGD have been used to annotate NBAS
  • Curation Notes: ClinVar Annotator: match by term: Infantile liver failure syndrome 2
  • Original References(s): PMID:25741868 PMID:26073778


    • An association has been curated linking NBAS and Infantile Liver Failure Syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:28878076 (Homo sapiens)
  • 1 RGD objects have been annotated to Infantile Liver Failure Syndrome 2  (DOID:9007272)
  • 5 papers in RGD have been used to annotate NBAS
  • Curation Notes: ClinVar Annotator: match by term: Infantile liver failure syndrome 2
  • Original References(s): PMID:25741868 PMID:28492532 PMID:32768688


    • An association has been curated linking NBAS and Infantile Liver Failure Syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13517024 (Homo sapiens)
  • 1 RGD objects have been annotated to Infantile Liver Failure Syndrome 2  (DOID:9007272)
  • 5 papers in RGD have been used to annotate NBAS
  • Curation Notes: ClinVar Annotator: match by term: Infantile liver failure syndrome 2
  • Original References(s): PMID:24033266 PMID:25741868 PMID:26073778 PMID:26541327 PMID:27789416 PMID:28031453 PMID:28492532 PMID:31761904


    • An association has been curated linking NBAS and Infantile Liver Failure Syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151788598 (Homo sapiens)
  • 1 RGD objects have been annotated to Infantile Liver Failure Syndrome 2  (DOID:9007272)
  • 5 papers in RGD have been used to annotate NBAS
  • Curation Notes: ClinVar Annotator: match by term: Infantile liver failure syndrome 2
  • Original References(s): PMID:25741868 PMID:28492532 PMID:32812336


    • An association has been curated linking NBAS and Infantile Liver Failure Syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13528584 (Homo sapiens)
  • 1 RGD objects have been annotated to Infantile Liver Failure Syndrome 2  (DOID:9007272)
  • 5 papers in RGD have been used to annotate NBAS
  • Curation Notes: ClinVar Annotator: match by term: Fever-associated acute infantile liver failure syndrome
  • Original References(s): PMID:24033266 PMID:25741868 PMID:26073778 PMID:26541327 PMID:27789416 PMID:28031453 PMID:28492532


    • An association has been curated linking NBAS and Infantile Liver Failure Syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:12911569 (Homo sapiens)
  • 1 RGD objects have been annotated to Infantile Liver Failure Syndrome 2  (DOID:9007272)
  • 5 papers in RGD have been used to annotate NBAS
  • Curation Notes: ClinVar Annotator: match by term: Infantile liver failure syndrome 2
  • Original References(s): PMID:28492532 PMID:28576691 PMID:33042920


    • An association has been curated linking NBAS and Infantile Liver Failure Syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:14393388 (Homo sapiens)
  • 1 RGD objects have been annotated to Infantile Liver Failure Syndrome 2  (DOID:9007272)
  • 5 papers in RGD have been used to annotate NBAS
  • Curation Notes: ClinVar Annotator: match by term: Infantile liver failure syndrome 2
  • Original References(s): PMID:25741868 PMID:26073778 PMID:26541327 PMID:27789416 PMID:28031453 PMID:28492532 PMID:30825388


    • An association has been curated linking NBAS and Infantile Liver Failure Syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:10056669 (Homo sapiens)
  • 1 RGD objects have been annotated to Infantile Liver Failure Syndrome 2  (DOID:9007272)
  • 5 papers in RGD have been used to annotate NBAS
  • Curation Notes: ClinVar Annotator: match by term: Infantile liver failure syndrome 2
  • Original References(s): PMID:25741868 PMID:26073778 PMID:28031453 PMID:28492532 PMID:34386911


    • An association has been curated linking NBAS and Infantile Liver Failure Syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:38598982 (Homo sapiens)
  • 1 RGD objects have been annotated to Infantile Liver Failure Syndrome 2  (DOID:9007272)
  • 5 papers in RGD have been used to annotate NBAS
  • Curation Notes: ClinVar Annotator: match by term: Infantile liver failure syndrome 2
  • Original References(s): PMID:26073778 PMID:26541327 PMID:27789416 PMID:28031453 PMID:28492532


    • An association has been curated linking NBAS and Infantile Liver Failure Syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:38598923 (Homo sapiens)
  • 1 RGD objects have been annotated to Infantile Liver Failure Syndrome 2  (DOID:9007272)
  • 5 papers in RGD have been used to annotate NBAS
  • Curation Notes: ClinVar Annotator: match by term: Infantile liver failure syndrome 2
  • Original References(s): PMID:16199547 PMID:26073778 PMID:26541327 PMID:27789416 PMID:28031453 PMID:28492532 PMID:32805445


    • An association has been curated linking NBAS and Infantile Liver Failure Syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151871585 (Homo sapiens)
  • 1 RGD objects have been annotated to Infantile Liver Failure Syndrome 2  (DOID:9007272)
  • 5 papers in RGD have been used to annotate NBAS
  • Curation Notes: ClinVar Annotator: match by term: Infantile liver failure syndrome 2
  • Original References(s): PMID:25741868 PMID:26073778 PMID:28492532 PMID:31761904


    • An association has been curated linking NBAS and Infantile Liver Failure Syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:26902583 (Homo sapiens)
  • 1 RGD objects have been annotated to Infantile Liver Failure Syndrome 2  (DOID:9007272)
  • 5 papers in RGD have been used to annotate NBAS
  • Curation Notes: ClinVar Annotator: match by term: Infantile liver failure syndrome 2
  • Original References(s): PMID:25741868 PMID:28492532 PMID:30558828 PMID:32313153


    • An association has been curated linking NBAS and Infantile Liver Failure Syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:12906850 (Homo sapiens)
  • 1 RGD objects have been annotated to Infantile Liver Failure Syndrome 2  (DOID:9007272)
  • 5 papers in RGD have been used to annotate NBAS
  • Curation Notes: ClinVar Annotator: match by term: Infantile liver failure syndrome 2
  • Original References(s): PMID:25741868 PMID:26073778 PMID:28492532


    • An association has been curated linking NBAS and Infantile Liver Failure Syndrome 2 in Homo sapiens.        

  • The association was inferred from experiment (EXP)
    		•  
  • The annotation was made from RGD automated import pipeline for CTD gene-to-disease annotations
  • 1 RGD objects have been annotated to Infantile Liver Failure Syndrome 2  (DOID:9007272)
  • 5 papers in RGD have been used to annotate NBAS
  • Curation Notes: CTD Direct Evidence: marker/mechanism


    • An association has been curated linking NBAS and Infantile Liver Failure Syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:10056667|RGD:10058936 (Homo sapiens) & RGD:10056667|RGD:10058936 (Homo sapiens)
  • 1 RGD objects have been annotated to Infantile Liver Failure Syndrome 2  (DOID:9007272)
  • 5 papers in RGD have been used to annotate NBAS
  • Curation Notes: ClinVar Annotator: match by term: Infantile liver failure syndrome 2
  • Original References(s): PMID:26073778


    • An association has been curated linking NBAS and Infantile Liver Failure Syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:12911812 (Homo sapiens)
  • 1 RGD objects have been annotated to Infantile Liver Failure Syndrome 2  (DOID:9007272)
  • 5 papers in RGD have been used to annotate NBAS
  • Curation Notes: ClinVar Annotator: match by term: Infantile liver failure syndrome 2
  • Original References(s): PMID:25741868 PMID:26073778 PMID:26541327 PMID:27789416 PMID:28031453 PMID:28492532 PMID:28576691


    • An association has been curated linking NBAS and Infantile Liver Failure Syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13437283|RGD:151235733|RGD:21075850 (Homo sapiens) & RGD:13437283|RGD:151235733|RGD:21075850 (Homo sapiens) & RGD:13437283|RGD:151235733|RGD:21075850 (Homo sapiens)
  • 1 RGD objects have been annotated to Infantile Liver Failure Syndrome 2  (DOID:9007272)
  • 5 papers in RGD have been used to annotate NBAS
  • Curation Notes: ClinVar Annotator: match by term: Infantile liver failure syndrome 2


    • An association has been curated linking NBAS and Infantile Liver Failure Syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:126732040|RGD:126735553|RGD:126735562|RGD:126735567|RGD:126912873|RGD:127303956|RGD:127308405|RGD:127310748|RGD:127314439|RGD:127318512|RGD:127318515|RGD:127318519|RGD:127318523|RGD:127318528|RGD:13529286|RGD:13610295|RGD:150447386|RGD:15166561|RGD:15176527|RGD:151844918|RGD:151853546|RGD:152139883|RGD:21066846 (Homo sapiens) & RGD:126732040|RGD:126735553|RGD:126735562|RGD:126735567|RGD:126912873|RGD:127303956|RGD:127308405|RGD:127310748|RGD:127314439|RGD:127318512|RGD:127318515|RGD:127318519|RGD:127318523|RGD:127318528|RGD:13529286|RGD:13610295|RGD:150447386|RGD:15166561|RGD:15176527|RGD:151844918|RGD:151853546|RGD:152139883|RGD:21066846 (Homo sapiens) & RGD:126732040|RGD:126735553|RGD:126735562|RGD:126735567|RGD:126912873|RGD:127303956|RGD:127308405|RGD:127310748|RGD:127314439|RGD:127318512|RGD:127318515|RGD:127318519|RGD:127318523|RGD:127318528|RGD:13529286|RGD:13610295|RGD:150447386|RGD:15166561|RGD:15176527|RGD:151844918|RGD:151853546|RGD:152139883|RGD:21066846 (Homo sapiens) & RGD:126732040|RGD:126735553|RGD:126735562|RGD:126735567|RGD:126912873|RGD:127303956|RGD:127308405|RGD:127310748|RGD:127314439|RGD:127318512|RGD:127318515|RGD:127318519|RGD:127318523|RGD:127318528|RGD:13529286|RGD:13610295|RGD:150447386|RGD:15166561|RGD:15176527|RGD:151844918|RGD:151853546|RGD:152139883|RGD:21066846 (Homo sapiens) & RGD:126732040|RGD:126735553|RGD:126735562|RGD:126735567|RGD:126912873|RGD:127303956|RGD:127308405|RGD:127310748|RGD:127314439|RGD:127318512|RGD:127318515|RGD:127318519|RGD:127318523|RGD:127318528|RGD:13529286|RGD:13610295|RGD:150447386|RGD:15166561|RGD:15176527|RGD:151844918|RGD:151853546|RGD:152139883|RGD:21066846 (Homo sapiens) & RGD:126732040|RGD:126735553|RGD:126735562|RGD:126735567|RGD:126912873|RGD:127303956|RGD:127308405|RGD:127310748|RGD:127314439|RGD:127318512|RGD:127318515|RGD:127318519|RGD:127318523|RGD:127318528|RGD:13529286|RGD:13610295|RGD:150447386|RGD:15166561|RGD:15176527|RGD:151844918|RGD:151853546|RGD:152139883|RGD:21066846 (Homo sapiens) & RGD:126732040|RGD:126735553|RGD:126735562|RGD:126735567|RGD:126912873|RGD:127303956|RGD:127308405|RGD:127310748|RGD:127314439|RGD:127318512|RGD:127318515|RGD:127318519|RGD:127318523|RGD:127318528|RGD:13529286|RGD:13610295|RGD:150447386|RGD:15166561|RGD:15176527|RGD:151844918|RGD:151853546|RGD:152139883|RGD:21066846 (Homo sapiens) & RGD:126732040|RGD:126735553|RGD:126735562|RGD:126735567|RGD:126912873|RGD:127303956|RGD:127308405|RGD:127310748|RGD:127314439|RGD:127318512|RGD:127318515|RGD:127318519|RGD:127318523|RGD:127318528|RGD:13529286|RGD:13610295|RGD:150447386|RGD:15166561|RGD:15176527|RGD:151844918|RGD:151853546|RGD:152139883|RGD:21066846 (Homo sapiens) & RGD:126732040|RGD:126735553|RGD:126735562|RGD:126735567|RGD:126912873|RGD:127303956|RGD:127308405|RGD:127310748|RGD:127314439|RGD:127318512|RGD:127318515|RGD:127318519|RGD:127318523|RGD:127318528|RGD:13529286|RGD:13610295|RGD:150447386|RGD:15166561|RGD:15176527|RGD:151844918|RGD:151853546|RGD:152139883|RGD:21066846 (Homo sapiens) & RGD:126732040|RGD:126735553|RGD:126735562|RGD:126735567|RGD:126912873|RGD:127303956|RGD:127308405|RGD:127310748|RGD:127314439|RGD:127318512|RGD:127318515|RGD:127318519|RGD:127318523|RGD:127318528|RGD:13529286|RGD:13610295|RGD:150447386|RGD:15166561|RGD:15176527|RGD:151844918|RGD:151853546|RGD:152139883|RGD:21066846 (Homo sapiens) & RGD:126732040|RGD:126735553|RGD:126735562|RGD:126735567|RGD:126912873|RGD:127303956|RGD:127308405|RGD:127310748|RGD:127314439|RGD:127318512|RGD:127318515|RGD:127318519|RGD:127318523|RGD:127318528|RGD:13529286|RGD:13610295|RGD:150447386|RGD:15166561|RGD:15176527|RGD:151844918|RGD:151853546|RGD:152139883|RGD:21066846 (Homo sapiens) & RGD:126732040|RGD:126735553|RGD:126735562|RGD:126735567|RGD:126912873|RGD:127303956|RGD:127308405|RGD:127310748|RGD:127314439|RGD:127318512|RGD:127318515|RGD:127318519|RGD:127318523|RGD:127318528|RGD:13529286|RGD:13610295|RGD:150447386|RGD:15166561|RGD:15176527|RGD:151844918|RGD:151853546|RGD:152139883|RGD:21066846 (Homo sapiens) & RGD:126732040|RGD:126735553|RGD:126735562|RGD:126735567|RGD:126912873|RGD:127303956|RGD:127308405|RGD:127310748|RGD:127314439|RGD:127318512|RGD:127318515|RGD:127318519|RGD:127318523|RGD:127318528|RGD:13529286|RGD:13610295|RGD:150447386|RGD:15166561|RGD:15176527|RGD:151844918|RGD:151853546|RGD:152139883|RGD:21066846 (Homo sapiens) & RGD:126732040|RGD:126735553|RGD:126735562|RGD:126735567|RGD:126912873|RGD:127303956|RGD:127308405|RGD:127310748|RGD:127314439|RGD:127318512|RGD:127318515|RGD:127318519|RGD:127318523|RGD:127318528|RGD:13529286|RGD:13610295|RGD:150447386|RGD:15166561|RGD:15176527|RGD:151844918|RGD:151853546|RGD:152139883|RGD:21066846 (Homo sapiens) & RGD:126732040|RGD:126735553|RGD:126735562|RGD:126735567|RGD:126912873|RGD:127303956|RGD:127308405|RGD:127310748|RGD:127314439|RGD:127318512|RGD:127318515|RGD:127318519|RGD:127318523|RGD:127318528|RGD:13529286|RGD:13610295|RGD:150447386|RGD:15166561|RGD:15176527|RGD:151844918|RGD:151853546|RGD:152139883|RGD:21066846 (Homo sapiens) & RGD:126732040|RGD:126735553|RGD:126735562|RGD:126735567|RGD:126912873|RGD:127303956|RGD:127308405|RGD:127310748|RGD:127314439|RGD:127318512|RGD:127318515|RGD:127318519|RGD:127318523|RGD:127318528|RGD:13529286|RGD:13610295|RGD:150447386|RGD:15166561|RGD:15176527|RGD:151844918|RGD:151853546|RGD:152139883|RGD:21066846 (Homo sapiens) & RGD:126732040|RGD:126735553|RGD:126735562|RGD:126735567|RGD:126912873|RGD:127303956|RGD:127308405|RGD:127310748|RGD:127314439|RGD:127318512|RGD:127318515|RGD:127318519|RGD:127318523|RGD:127318528|RGD:13529286|RGD:13610295|RGD:150447386|RGD:15166561|RGD:15176527|RGD:151844918|RGD:151853546|RGD:152139883|RGD:21066846 (Homo sapiens) & RGD:126732040|RGD:126735553|RGD:126735562|RGD:126735567|RGD:126912873|RGD:127303956|RGD:127308405|RGD:127310748|RGD:127314439|RGD:127318512|RGD:127318515|RGD:127318519|RGD:127318523|RGD:127318528|RGD:13529286|RGD:13610295|RGD:150447386|RGD:15166561|RGD:15176527|RGD:151844918|RGD:151853546|RGD:152139883|RGD:21066846 (Homo sapiens) & RGD:126732040|RGD:126735553|RGD:126735562|RGD:126735567|RGD:126912873|RGD:127303956|RGD:127308405|RGD:127310748|RGD:127314439|RGD:127318512|RGD:127318515|RGD:127318519|RGD:127318523|RGD:127318528|RGD:13529286|RGD:13610295|RGD:150447386|RGD:15166561|RGD:15176527|RGD:151844918|RGD:151853546|RGD:152139883|RGD:21066846 (Homo sapiens) & RGD:126732040|RGD:126735553|RGD:126735562|RGD:126735567|RGD:126912873|RGD:127303956|RGD:127308405|RGD:127310748|RGD:127314439|RGD:127318512|RGD:127318515|RGD:127318519|RGD:127318523|RGD:127318528|RGD:13529286|RGD:13610295|RGD:150447386|RGD:15166561|RGD:15176527|RGD:151844918|RGD:151853546|RGD:152139883|RGD:21066846 (Homo sapiens) & RGD:126732040|RGD:126735553|RGD:126735562|RGD:126735567|RGD:126912873|RGD:127303956|RGD:127308405|RGD:127310748|RGD:127314439|RGD:127318512|RGD:127318515|RGD:127318519|RGD:127318523|RGD:127318528|RGD:13529286|RGD:13610295|RGD:150447386|RGD:15166561|RGD:15176527|RGD:151844918|RGD:151853546|RGD:152139883|RGD:21066846 (Homo sapiens) & RGD:126732040|RGD:126735553|RGD:126735562|RGD:126735567|RGD:126912873|RGD:127303956|RGD:127308405|RGD:127310748|RGD:127314439|RGD:127318512|RGD:127318515|RGD:127318519|RGD:127318523|RGD:127318528|RGD:13529286|RGD:13610295|RGD:150447386|RGD:15166561|RGD:15176527|RGD:151844918|RGD:151853546|RGD:152139883|RGD:21066846 (Homo sapiens) & RGD:126732040|RGD:126735553|RGD:126735562|RGD:126735567|RGD:126912873|RGD:127303956|RGD:127308405|RGD:127310748|RGD:127314439|RGD:127318512|RGD:127318515|RGD:127318519|RGD:127318523|RGD:127318528|RGD:13529286|RGD:13610295|RGD:150447386|RGD:15166561|RGD:15176527|RGD:151844918|RGD:151853546|RGD:152139883|RGD:21066846 (Homo sapiens)
  • 1 RGD objects have been annotated to Infantile Liver Failure Syndrome 2  (DOID:9007272)
  • 5 papers in RGD have been used to annotate NBAS
  • Curation Notes: ClinVar Annotator: match by term: Infantile liver failure syndrome 2
  • Original References(s): PMID:25741868 PMID:28492532


    • An association has been curated linking NBAS and Infantile Liver Failure Syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:126767307|RGD:21075848|RGD:21075849 (Homo sapiens) & RGD:126767307|RGD:21075848|RGD:21075849 (Homo sapiens) & RGD:126767307|RGD:21075848|RGD:21075849 (Homo sapiens)
  • 1 RGD objects have been annotated to Infantile Liver Failure Syndrome 2  (DOID:9007272)
  • 5 papers in RGD have been used to annotate NBAS
  • Curation Notes: ClinVar Annotator: match by term: Infantile liver failure syndrome 2
  • Original References(s): PMID:28492532


    • An association has been curated linking NBAS and Infantile Liver Failure Syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:26902585 (Homo sapiens)
  • 1 RGD objects have been annotated to Infantile Liver Failure Syndrome 2  (DOID:9007272)
  • 5 papers in RGD have been used to annotate NBAS
  • Curation Notes: ClinVar Annotator: match by term: Infantile liver failure syndrome 2
  • Original References(s): PMID:25741868 PMID:30558828 PMID:32313153


    • An association has been curated linking NBAS and Infantile Liver Failure Syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:10056668 (Homo sapiens)
  • 1 RGD objects have been annotated to Infantile Liver Failure Syndrome 2  (DOID:9007272)
  • 5 papers in RGD have been used to annotate NBAS
  • Curation Notes: ClinVar Annotator: match by term: Infantile liver failure syndrome 2
  • Original References(s): PMID:25741868 PMID:26073778 PMID:26541327 PMID:27789416 PMID:28031453 PMID:28252636 PMID:28492532 PMID:30825388


    • An association has been curated linking NBAS and Infantile Liver Failure Syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:150448205|RGD:150448207 (Homo sapiens) & RGD:150448205|RGD:150448207 (Homo sapiens)
  • 1 RGD objects have been annotated to Infantile Liver Failure Syndrome 2  (DOID:9007272)
  • 5 papers in RGD have been used to annotate NBAS
  • Curation Notes: ClinVar Annotator: match by term: Infantile liver failure syndrome 2
  • Original References(s): PMID:25741868 PMID:34298581


    • An association has been curated linking NBAS and Infantile Liver Failure Syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:10449629 (Homo sapiens)
  • 1 RGD objects have been annotated to Infantile Liver Failure Syndrome 2  (DOID:9007272)
  • 5 papers in RGD have been used to annotate NBAS
  • Curation Notes: ClinVar Annotator: match by term: Infantile liver failure syndrome 2
  • Original References(s): PMID:25741868 PMID:26286438 PMID:26541327 PMID:26578240 PMID:28410752 PMID:28492532 PMID:28576691 PMID:31964843 PMID:34906502


    • An association has been curated linking NBAS and Infantile Liver Failure Syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:14393389 (Homo sapiens)
  • 1 RGD objects have been annotated to Infantile Liver Failure Syndrome 2  (DOID:9007272)
  • 5 papers in RGD have been used to annotate NBAS
  • Curation Notes: ClinVar Annotator: match by term: Infantile liver failure syndrome 2
  • Original References(s): PMID:17576681 PMID:25741868 PMID:28492532 PMID:30825388 PMID:31761904 PMID:33042920 PMID:9536098


    • An association has been curated linking NBAS and Infantile Liver Failure Syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:126735557|RGD:150332770|RGD:150431286|RGD:150442932|RGD:150449051|RGD:150477768|RGD:150535955|RGD:152979514|RGD:152999194|RGD:152999234|RGD:153302141|RGD:243050603|RGD:243050766 (Homo sapiens) & RGD:126735557|RGD:150332770|RGD:150431286|RGD:150442932|RGD:150449051|RGD:150477768|RGD:150535955|RGD:152979514|RGD:152999194|RGD:152999234|RGD:153302141|RGD:243050603|RGD:243050766 (Homo sapiens) & RGD:126735557|RGD:150332770|RGD:150431286|RGD:150442932|RGD:150449051|RGD:150477768|RGD:150535955|RGD:152979514|RGD:152999194|RGD:152999234|RGD:153302141|RGD:243050603|RGD:243050766 (Homo sapiens) & RGD:126735557|RGD:150332770|RGD:150431286|RGD:150442932|RGD:150449051|RGD:150477768|RGD:150535955|RGD:152979514|RGD:152999194|RGD:152999234|RGD:153302141|RGD:243050603|RGD:243050766 (Homo sapiens) & RGD:126735557|RGD:150332770|RGD:150431286|RGD:150442932|RGD:150449051|RGD:150477768|RGD:150535955|RGD:152979514|RGD:152999194|RGD:152999234|RGD:153302141|RGD:243050603|RGD:243050766 (Homo sapiens) & RGD:126735557|RGD:150332770|RGD:150431286|RGD:150442932|RGD:150449051|RGD:150477768|RGD:150535955|RGD:152979514|RGD:152999194|RGD:152999234|RGD:153302141|RGD:243050603|RGD:243050766 (Homo sapiens) & RGD:126735557|RGD:150332770|RGD:150431286|RGD:150442932|RGD:150449051|RGD:150477768|RGD:150535955|RGD:152979514|RGD:152999194|RGD:152999234|RGD:153302141|RGD:243050603|RGD:243050766 (Homo sapiens) & RGD:126735557|RGD:150332770|RGD:150431286|RGD:150442932|RGD:150449051|RGD:150477768|RGD:150535955|RGD:152979514|RGD:152999194|RGD:152999234|RGD:153302141|RGD:243050603|RGD:243050766 (Homo sapiens) & RGD:126735557|RGD:150332770|RGD:150431286|RGD:150442932|RGD:150449051|RGD:150477768|RGD:150535955|RGD:152979514|RGD:152999194|RGD:152999234|RGD:153302141|RGD:243050603|RGD:243050766 (Homo sapiens) & RGD:126735557|RGD:150332770|RGD:150431286|RGD:150442932|RGD:150449051|RGD:150477768|RGD:150535955|RGD:152979514|RGD:152999194|RGD:152999234|RGD:153302141|RGD:243050603|RGD:243050766 (Homo sapiens) & RGD:126735557|RGD:150332770|RGD:150431286|RGD:150442932|RGD:150449051|RGD:150477768|RGD:150535955|RGD:152979514|RGD:152999194|RGD:152999234|RGD:153302141|RGD:243050603|RGD:243050766 (Homo sapiens) & RGD:126735557|RGD:150332770|RGD:150431286|RGD:150442932|RGD:150449051|RGD:150477768|RGD:150535955|RGD:152979514|RGD:152999194|RGD:152999234|RGD:153302141|RGD:243050603|RGD:243050766 (Homo sapiens) & RGD:126735557|RGD:150332770|RGD:150431286|RGD:150442932|RGD:150449051|RGD:150477768|RGD:150535955|RGD:152979514|RGD:152999194|RGD:152999234|RGD:153302141|RGD:243050603|RGD:243050766 (Homo sapiens)
  • 1 RGD objects have been annotated to Infantile Liver Failure Syndrome 2  (DOID:9007272)
  • 5 papers in RGD have been used to annotate NBAS
  • Curation Notes: ClinVar Annotator: match by term: Infantile liver failure syndrome 2
  • Original References(s): PMID:25741868


    • An association has been curated linking NBAS and Infantile Liver Failure Syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151821923|RGD:151839289 (Homo sapiens) & RGD:151821923|RGD:151839289 (Homo sapiens)
  • 1 RGD objects have been annotated to Infantile Liver Failure Syndrome 2  (DOID:9007272)
  • 5 papers in RGD have been used to annotate NBAS
  • Curation Notes: ClinVar Annotator: match by term: Infantile liver failure syndrome 2
  • Original References(s): PMID:25741868 PMID:26073778 PMID:26541327 PMID:27789416 PMID:28031453 PMID:28492532 PMID:31761904


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