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GENE - TERM ANNOTATION REPORT

4 Annotations Found.

An association has been curated linking Gnas and pseudopseudohypoparathyroidism 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 GNAS (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to pseudopseudohypoparathyroidism  (DOID:4183)
  • 44 papers in RGD have been used to annotate Gnas


    • An association has been curated linking Gnas and pseudopseudohypoparathyroidism 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 GNAS (Homo sapiens) [(EXP) inferred from experiment]
  • 2 RGD objects have been annotated to pseudopseudohypoparathyroidism  (DOID:4183)
  • 44 papers in RGD have been used to annotate Gnas
  • Curation Notes: CTD Direct Evidence: marker/mechanism
  • Original References(s): PMID:9506752


    • An association has been curated linking Gnas and pseudopseudohypoparathyroidism in Mus musculus.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for MGI gene-to-disease annotations
  • 2 RGD objects have been annotated to pseudopseudohypoparathyroidism  (DOID:4183)
  • 44 papers in RGD have been used to annotate Gnas
  • Curation Notes: OMIM:612463


    • An association has been curated linking Gnas and pseudopseudohypoparathyroidism 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 GNAS (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to pseudopseudohypoparathyroidism  (DOID:4183)
  • 44 papers in RGD have been used to annotate Gnas
  • Curation Notes: ClinVar Annotator: match by term: Albright hereditary osteodystrophy without multiple hormone resistance | ClinVar Annotator: match by term: Pseudopseudohypoparathyroidism
  • Original References(s): PMID:10487696 PMID:11092390 PMID:11095461 PMID:11600516 PMID:11784876 PMID:12024004 PMID:12621129 PMID:12624854 PMID:1505964 PMID:15711092 PMID:16199547 PMID:18553568 PMID:18796523 PMID:20427508 PMID:2122458 PMID:21274345 PMID:21525160 PMID:219790 PMID:23281139 PMID:23533243 PMID:23796510 PMID:23884777 PMID:24033266 PMID:24088041 PMID:24481334 PMID:24626099 PMID:24728327 PMID:25044890 PMID:25219572 PMID:25594858 PMID:25741868 PMID:25802881 PMID:26633545 PMID:27703483 PMID:28296742 PMID:28492532 PMID:28708303 PMID:29059381 PMID:29072892 PMID:29095814 PMID:30349702 PMID:30674755 PMID:30729047 PMID:31793173 PMID:31886927 PMID:33144682 PMID:34008892 PMID:34254228 PMID:34418133 PMID:34614324 PMID:35296306 PMID:35357904 PMID:35497370 PMID:7853365 PMID:8702665 PMID:9506752 PMID:9727013 PMID:9876352


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