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GENE - TERM ANNOTATION REPORT

32 Annotations Found.

An association has been curated linking Ghr and Laron syndrome 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 GHR (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to Laron syndrome  (DOID:9521)
  • 63 papers in RGD have been used to annotate Ghr
  • Curation Notes: ClinVar Annotator: match by term: Laron syndrome with elevated serum gh-binding protein
  • Original References(s): PMID:8626815


  • An association has been curated linking Ghr and Laron syndrome 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 GHR (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to Laron syndrome  (DOID:9521)
  • 63 papers in RGD have been used to annotate Ghr
  • Curation Notes: ClinVar Annotator: match by term: Laron syndrome with elevated serum gh-binding protein
  • Original References(s): PMID:10084588, PMID:9467570


  • An association has been curated linking Ghr and Laron syndrome in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from Zhou Y, etal., Proc Natl Acad Sci U S A. 1997 Nov 25;94(24):13215-20.
  • The annotation has been inferred from sequence orthology with Ghr (Mus musculus) [(IMP) inferred from mutant phenotype]
  • 2 additional annotations were made from Zhou Y, etal., Proc Natl Acad Sci U S A. 1997 Nov 25;94(24):13215-20.
  • 2 RGD objects have been annotated to Laron syndrome  (DOID:9521)
  • 63 papers in RGD have been used to annotate Ghr


  • An association has been curated linking Ghr and Laron syndrome 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 GHR (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to Laron syndrome  (DOID:9521)
  • 63 papers in RGD have been used to annotate Ghr


  • An association has been curated linking Ghr and Laron syndrome 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 GHR (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to Laron syndrome  (DOID:9521)
  • 63 papers in RGD have been used to annotate Ghr
  • Curation Notes: ClinVar Annotator: match by OMIM:262500
  • Original References(s): PMID:17405847


  • An association has been curated linking Ghr and Laron syndrome 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 GHR (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to Laron syndrome  (DOID:9521)
  • 63 papers in RGD have been used to annotate Ghr
  • Curation Notes: ClinVar Annotator: match by OMIM:262500
  • Original References(s): PMID:12679461


  • An association has been curated linking Ghr and Laron syndrome 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 GHR (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to Laron syndrome  (DOID:9521)
  • 63 papers in RGD have been used to annotate Ghr
  • Curation Notes: ClinVar Annotator: match by OMIM:262500
  • Original References(s): PMID:15536163


  • An association has been curated linking Ghr and Laron syndrome 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 GHR (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to Laron syndrome  (DOID:9521)
  • 63 papers in RGD have been used to annotate Ghr
  • Curation Notes: ClinVar Annotator: match by OMIM:262500
  • Original References(s): PMID:1719554, PMID:2779634, PMID:8450064


  • An association has been curated linking Ghr and Laron syndrome 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 GHR (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to Laron syndrome  (DOID:9521)
  • 63 papers in RGD have been used to annotate Ghr
  • Curation Notes: ClinVar Annotator: match by OMIM:262500
  • Original References(s): PMID:9851797


  • An association has been curated linking Ghr and Laron syndrome 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 GHR (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to Laron syndrome  (DOID:9521)
  • 63 papers in RGD have been used to annotate Ghr
  • Curation Notes: ClinVar Annotator: match by OMIM:262500
  • Original References(s): PMID:1999489


  • An association has been curated linking Ghr and Laron syndrome 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 GHR (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to Laron syndrome  (DOID:9521)
  • 63 papers in RGD have been used to annotate Ghr
  • Curation Notes: ClinVar Annotator: match by OMIM:262500
  • Original References(s): PMID:11836282, PMID:1284474, PMID:2233903, PMID:9626125, PMID:9661611


  • An association has been curated linking Ghr and Laron syndrome 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 GHR (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to Laron syndrome  (DOID:9521)
  • 63 papers in RGD have been used to annotate Ghr
  • Curation Notes: ClinVar Annotator: match by OMIM:262500
  • Original References(s): PMID:8488849


  • An association has been curated linking Ghr and Laron syndrome 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 GHR (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to Laron syndrome  (DOID:9521)
  • 63 papers in RGD have been used to annotate Ghr
  • Curation Notes: ClinVar Annotator: match by OMIM:262500
  • Original References(s): PMID:15001620


  • An association has been curated linking Ghr and Laron syndrome 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 GHR (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to Laron syndrome  (DOID:9521)
  • 63 papers in RGD have been used to annotate Ghr
  • Curation Notes: ClinVar Annotator: match by OMIM:262500
  • Original References(s): PMID:11468686, PMID:17148568


  • An association has been curated linking Ghr and Laron syndrome 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 GHR (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to Laron syndrome  (DOID:9521)
  • 63 papers in RGD have been used to annotate Ghr
  • Curation Notes: ClinVar Annotator: match by OMIM:262500
  • Original References(s): PMID:1999489, PMID:8488849


  • An association has been curated linking Ghr and Laron syndrome 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 GHR (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to Laron syndrome  (DOID:9521)
  • 63 papers in RGD have been used to annotate Ghr
  • Curation Notes: ClinVar Annotator: match by OMIM:262500
  • Original References(s): PMID:2813379


  • An association has been curated linking Ghr and Laron syndrome 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 GHR (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to Laron syndrome  (DOID:9521)
  • 63 papers in RGD have been used to annotate Ghr
  • Curation Notes: ClinVar Annotator: match by term: Laron Syndrome
  • Original References(s): PMID:11395710, PMID:12181638, PMID:16213173, PMID:17547682, PMID:19344888, PMID:19447840, PMID:26467025, PMID:8421103, PMID:8664975


  • An association has been curated linking Ghr and Laron syndrome 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 GHR (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to Laron syndrome  (DOID:9521)
  • 63 papers in RGD have been used to annotate Ghr
  • Curation Notes: ClinVar Annotator: match by term: Laron Syndrome
  • Original References(s): PMID:25741868, PMID:26467025


  • An association has been curated linking Ghr and Laron syndrome in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from Klammt J, etal., Clin Endocrinol (Oxf). 2015 Mar;82(3):453-61. doi: 10.1111/cen.12606. Epub 2014 Oct 20.
  • The annotation has been inferred from sequence orthology with GHR (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype, (IEP) inferred from expression pattern]
  • 3 additional annotations were made from Klammt J, etal., Clin Endocrinol (Oxf). 2015 Mar;82(3):453-61. doi: 10.1111/cen.12606. Epub 2014 Oct 20.
  • 2 RGD objects have been annotated to Laron syndrome  (DOID:9521)
  • 63 papers in RGD have been used to annotate Ghr
  • Curation Notes: DNA:deletion:exon,intron:


  • An association has been curated linking Ghr and Laron syndrome 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 GHR (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to Laron syndrome  (DOID:9521)
  • 63 papers in RGD have been used to annotate Ghr
  • Curation Notes: ClinVar Annotator: match by term: Laron syndrome with undetectable serum GH-binding protein
  • Original References(s): PMID:9360529


  • An association has been curated linking Ghr and Laron syndrome 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 GHR (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to Laron syndrome  (DOID:9521)
  • 63 papers in RGD have been used to annotate Ghr
  • Curation Notes: ClinVar Annotator: match by term: Laron syndrome with undetectable serum GH-binding protein
  • Original References(s): PMID:9661642


  • An association has been curated linking Ghr and Laron syndrome in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from Sobrier ML, etal., J Clin Endocrinol Metab. 1997 Feb;82(2):435-7.
  • The annotation has been inferred from sequence orthology with GHR (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 additional annotations were made from Sobrier ML, etal., J Clin Endocrinol Metab. 1997 Feb;82(2):435-7.
  • 2 RGD objects have been annotated to Laron syndrome  (DOID:9521)
  • 63 papers in RGD have been used to annotate Ghr
  • Curation Notes: DNA:nonsense, missense, deletion mutations:cds, splice junction:


  • An association has been curated linking Ghr and Laron syndrome 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 GHR (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to Laron syndrome  (DOID:9521)
  • 63 papers in RGD have been used to annotate Ghr
  • Curation Notes: ClinVar Annotator: match by OMIM:262500


  • An association has been curated linking Ghr and Laron syndrome 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 GHR (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to Laron syndrome  (DOID:9521)
  • 63 papers in RGD have been used to annotate Ghr
  • Curation Notes: ClinVar Annotator: match by term: Laron Syndrome
  • Original References(s): PMID:25741868


  • An association has been curated linking Ghr and Laron syndrome 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 GHR (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to Laron syndrome  (DOID:9521)
  • 63 papers in RGD have been used to annotate Ghr
  • Curation Notes: ClinVar Annotator: match by term: Laron-type isolated somatotropin defect
  • Original References(s): PMID:10984309, PMID:25741868, PMID:30311386


  • An association has been curated linking Ghr and Laron syndrome 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 GHR (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to Laron syndrome  (DOID:9521)
  • 63 papers in RGD have been used to annotate Ghr
  • Curation Notes: ClinVar Annotator: match by term: Laron-type isolated somatotropin defect
  • Original References(s): PMID:28492532


  • An association has been curated linking Ghr and Laron syndrome 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 GHR (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to Laron syndrome  (DOID:9521)
  • 63 papers in RGD have been used to annotate Ghr
  • Curation Notes: ClinVar Annotator: match by term: Laron-type isolated somatotropin defect
  • Original References(s): PMID:25741868, PMID:28492532


  • An association has been curated linking Ghr and Laron syndrome 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 GHR (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to Laron syndrome  (DOID:9521)
  • 63 papers in RGD have been used to annotate Ghr
  • Curation Notes: ClinVar Annotator: match by term: Laron-type isolated somatotropin defect
  • Original References(s): PMID:17462934, PMID:25741868, PMID:28492532, PMID:7565946, PMID:8504296


  • An association has been curated linking Ghr and Laron syndrome 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 GHR (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to Laron syndrome  (DOID:9521)
  • 63 papers in RGD have been used to annotate Ghr
  • Curation Notes: ClinVar Annotator: match by term: Laron-type isolated somatotropin defect
  • Original References(s): PMID:12217488, PMID:21525302, PMID:24150201, PMID:26467025, PMID:27408750, PMID:28492532, PMID:28498917, PMID:9814495


  • An association has been curated linking Ghr and Laron syndrome 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 GHR (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to Laron syndrome  (DOID:9521)
  • 63 papers in RGD have been used to annotate Ghr
  • Curation Notes: ClinVar Annotator: match by term: Laron-type isolated somatotropin defect
  • Original References(s): PMID:11785980, PMID:9360529


  • An association has been curated linking Ghr and Laron syndrome 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 GHR (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to Laron syndrome  (DOID:9521)
  • 63 papers in RGD have been used to annotate Ghr
  • Curation Notes: ClinVar Annotator: match by term: Laron-type isolated somatotropin defect
  • Original References(s): PMID:21846964, PMID:21900382, PMID:25741868, PMID:28492532, PMID:7565946


  • An association has been curated linking Ghr and Laron syndrome 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 GHR (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to Laron syndrome  (DOID:9521)
  • 63 papers in RGD have been used to annotate Ghr
  • Curation Notes: ClinVar Annotator: match by term: Laron-type isolated somatotropin defect
  • Original References(s): PMID:20962506


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