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GENE - TERM ANNOTATION REPORT

5 Annotations Found.

An association has been curated linking Mab21l1 and Cerebellar, Ocular, Craniofacial, and Genital 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 MAB21L1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to Cerebellar, Ocular, Craniofacial, and Genital Syndrome  (DOID:9008126)
  • 1 papers in RGD have been used to annotate Mab21l1


  • An association has been curated linking Mab21l1 and Cerebellar, Ocular, Craniofacial, and Genital 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 MAB21L1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to Cerebellar, Ocular, Craniofacial, and Genital Syndrome  (DOID:9008126)
  • 1 papers in RGD have been used to annotate Mab21l1
  • Curation Notes: ClinVar Annotator: match by term: CEREBELLAR, OCULAR, CRANIOFACIAL, AND GENITAL SYNDROME
  • Original References(s): PMID:23374822 PMID:27075597 PMID:30487245


  • An association has been curated linking Mab21l1 and Cerebellar, Ocular, Craniofacial, and Genital 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 MAB21L1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to Cerebellar, Ocular, Craniofacial, and Genital Syndrome  (DOID:9008126)
  • 1 papers in RGD have been used to annotate Mab21l1
  • Curation Notes: ClinVar Annotator: match by term: CEREBELLAR, OCULAR, CRANIOFACIAL, AND GENITAL SYNDROME
  • Original References(s): PMID:30487245


  • An association has been curated linking Mab21l1 and Cerebellar, Ocular, Craniofacial, and Genital 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 MAB21L1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to Cerebellar, Ocular, Craniofacial, and Genital Syndrome  (DOID:9008126)
  • 1 papers in RGD have been used to annotate Mab21l1
  • Curation Notes: ClinVar Annotator: match by term: CEREBELLAR, OCULAR, CRANIOFACIAL, AND GENITAL SYNDROME
  • Original References(s): PMID:27075597 PMID:30487245


  • An association has been curated linking Mab21l1 and Cerebellar, Ocular, Craniofacial, and Genital 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 MAB21L1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to Cerebellar, Ocular, Craniofacial, and Genital Syndrome  (DOID:9008126)
  • 1 papers in RGD have been used to annotate Mab21l1
  • Curation Notes: ClinVar Annotator: match by term: CEREBELLAR, OCULAR, CRANIOFACIAL, AND GENITAL SYNDROME
  • Original References(s): PMID:27103078


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