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GENE - TERM ANNOTATION REPORT

10 Annotations Found.

An association has been curated linking Fgfr1 and Holoprosencephaly, Ectrodactyly, and Bilateral Cleft Lip/Palate 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 FGFR1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Holoprosencephaly, Ectrodactyly, and Bilateral Cleft Lip/Palate  (DOID:9004955)
  • 100 papers in RGD have been used to annotate Fgfr1
  • Curation Notes: ClinVar Annotator: match by term: Hartsfield syndrome


  • An association has been curated linking Fgfr1 and Holoprosencephaly, Ectrodactyly, and Bilateral Cleft Lip/Palate 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 FGFR1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Holoprosencephaly, Ectrodactyly, and Bilateral Cleft Lip/Palate  (DOID:9004955)
  • 100 papers in RGD have been used to annotate Fgfr1
  • Curation Notes: ClinVar Annotator: match by null
  • Original References(s): PMID:19504604 PMID:23812909


  • An association has been curated linking Fgfr1 and Holoprosencephaly, Ectrodactyly, and Bilateral Cleft Lip/Palate 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 FGFR1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Holoprosencephaly, Ectrodactyly, and Bilateral Cleft Lip/Palate  (DOID:9004955)
  • 100 papers in RGD have been used to annotate Fgfr1
  • Curation Notes: ClinVar Annotator: match by null
  • Original References(s): PMID:23812909


  • An association has been curated linking Fgfr1 and Holoprosencephaly, Ectrodactyly, and Bilateral Cleft Lip/Palate 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 FGFR1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Holoprosencephaly, Ectrodactyly, and Bilateral Cleft Lip/Palate  (DOID:9004955)
  • 100 papers in RGD have been used to annotate Fgfr1


  • An association has been curated linking Fgfr1 and Holoprosencephaly, Ectrodactyly, and Bilateral Cleft Lip/Palate 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 FGFR1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Holoprosencephaly, Ectrodactyly, and Bilateral Cleft Lip/Palate  (DOID:9004955)
  • 100 papers in RGD have been used to annotate Fgfr1
  • Curation Notes: ClinVar Annotator: match by term: Hartsfield syndrome
  • Original References(s): PMID:24888332 PMID:25326635 PMID:25741868 PMID:26931467


  • An association has been curated linking Fgfr1 and Holoprosencephaly, Ectrodactyly, and Bilateral Cleft Lip/Palate 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 FGFR1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Holoprosencephaly, Ectrodactyly, and Bilateral Cleft Lip/Palate  (DOID:9004955)
  • 100 papers in RGD have been used to annotate Fgfr1
  • Curation Notes: ClinVar Annotator: match by term: Hartsfield syndrome
  • Original References(s): PMID:24204987 PMID:26931467


  • An association has been curated linking Fgfr1 and Holoprosencephaly, Ectrodactyly, and Bilateral Cleft Lip/Palate 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 FGFR1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Holoprosencephaly, Ectrodactyly, and Bilateral Cleft Lip/Palate  (DOID:9004955)
  • 100 papers in RGD have been used to annotate Fgfr1
  • Curation Notes: ClinVar Annotator: match by term: Hartsfield syndrome
  • Original References(s): PMID:26931467


  • An association has been curated linking Fgfr1 and Holoprosencephaly, Ectrodactyly, and Bilateral Cleft Lip/Palate 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 FGFR1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Holoprosencephaly, Ectrodactyly, and Bilateral Cleft Lip/Palate  (DOID:9004955)
  • 100 papers in RGD have been used to annotate Fgfr1
  • Curation Notes: ClinVar Annotator: match by term: Hartsfield syndrome
  • Original References(s): PMID:25741868


  • An association has been curated linking Fgfr1 and Holoprosencephaly, Ectrodactyly, and Bilateral Cleft Lip/Palate 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 FGFR1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Holoprosencephaly, Ectrodactyly, and Bilateral Cleft Lip/Palate  (DOID:9004955)
  • 100 papers in RGD have been used to annotate Fgfr1
  • Curation Notes: ClinVar Annotator: match by term: Hartsfield syndrome
  • Original References(s): PMID:15605412 PMID:16764984 PMID:23657145 PMID:25064402 PMID:26931467 PMID:28492532


  • An association has been curated linking Fgfr1 and Holoprosencephaly, Ectrodactyly, and Bilateral Cleft Lip/Palate 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 FGFR1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Holoprosencephaly, Ectrodactyly, and Bilateral Cleft Lip/Palate  (DOID:9004955)
  • 100 papers in RGD have been used to annotate Fgfr1
  • Curation Notes: ClinVar Annotator: match by term: Hartsfield syndrome
  • Original References(s): PMID:31474318


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