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GENE - TERM ANNOTATION REPORT

2 Annotations Found.

An association has been curated linking Marveld2 and autosomal recessive nonsyndromic deafness 49 in Ictidomys tridecemlineatus.        

  • 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 MARVELD2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to autosomal recessive nonsyndromic deafness 49  (DOID:0110506)
  • 0 papers in RGD have been used to annotate Marveld2


    • An association has been curated linking Marveld2 and autosomal recessive nonsyndromic deafness 49 in Ictidomys tridecemlineatus.        

  • 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 MARVELD2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to autosomal recessive nonsyndromic deafness 49  (DOID:0110506)
  • 0 papers in RGD have been used to annotate Marveld2
  • Curation Notes: ClinVar Annotator: match by term: Deafness, autosomal recessive 49 | ClinVar Annotator: match by term: Deafness, neurosensory, autosomal recessive 49
  • Original References(s): PMID:16199547 PMID:17186462 PMID:18084694 PMID:22097895 PMID:23767834 PMID:23979167 PMID:24033266 PMID:25652404 PMID:25666562 PMID:25741868 PMID:25788563 PMID:25885414 PMID:26467025 PMID:28492532 PMID:30311386 PMID:31850270 PMID:32747562 PMID:33597575


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