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GENE - TERM ANNOTATION REPORT

4 Annotations Found.

An association has been curated linking Mid1 and Opitz GBBB 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 MID1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Opitz GBBB syndrome  (DOID:0080697)
  • 11 papers in RGD have been used to annotate Mid1


    • An association has been curated linking Mid1 and Opitz GBBB 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 MID1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Opitz GBBB syndrome  (DOID:0080697)
  • 11 papers in RGD have been used to annotate Mid1
  • Curation Notes: ClinVar Annotator: match by term: OPITZ-G SYNDROME, TYPE I
  • Original References(s): PMID:11030761 PMID:12545276 PMID:15121778 PMID:15558842 PMID:17221865 PMID:18360914 PMID:18949047 PMID:20671548 PMID:21326312 PMID:23757202 PMID:25207814 PMID:25304119 PMID:25741868 PMID:25874572 PMID:27749392 PMID:28492532 PMID:29456483 PMID:32926417 PMID:9354791


    • An association has been curated linking Mid1 and Opitz GBBB syndrome in Rattus norvegicus.        

  • The association was inferred from sequence or structural similarity (ISS)
    		•  
  • The annotation was made from RGD automated import pipeline for MGI gene-to-disease annotations
  • The annotation has been inferred from sequence or structural similarity with Mid1 (Mus musculus) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Opitz GBBB syndrome  (DOID:0080697)
  • 11 papers in RGD have been used to annotate Mid1
  • Curation Notes: OMIM:300000


    • An association has been curated linking Mid1 and Opitz GBBB syndrome in Rattus norvegicus.        

  • 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 MID1 (Homo sapiens) [(EXP) inferred from experiment]
  • 1 RGD objects have been annotated to Opitz GBBB syndrome  (DOID:0080697)
  • 11 papers in RGD have been used to annotate Mid1
  • Curation Notes: CTD Direct Evidence: marker/mechanism


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