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GENE - TERM ANNOTATION REPORT

2 Annotations Found.

An association has been curated linking Ofd1 and Simpson-Golabi-Behmel syndrome type 2 in Heterocephalus glaber.        

  • 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 OFD1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Simpson-Golabi-Behmel syndrome type 2  (DOID:0080342)
  • 0 papers in RGD have been used to annotate Ofd1


    • An association has been curated linking Ofd1 and Simpson-Golabi-Behmel syndrome type 2 in Heterocephalus glaber.        

  • 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 OFD1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Simpson-Golabi-Behmel syndrome type 2  (DOID:0080342)
  • 0 papers in RGD have been used to annotate Ofd1
  • Curation Notes: ClinVar Annotator: match by term: Simpson-Golabi-Behmel syndrome type 2
  • Original References(s): PMID:11179005 PMID:12595504 PMID:16783569 PMID:18546297 PMID:19800048 PMID:22353940 PMID:23033313 PMID:25741868 PMID:26467025 PMID:28492532 PMID:30401917 PMID:33847015 PMID:35112477


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