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GENE - TERM ANNOTATION REPORT

5 Annotations Found.

An association has been curated linking BC052040 and congenital dyserythropoietic anemia type Ib 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 C15orf41 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 CRRD objects have been annotated to congenital dyserythropoietic anemia type Ib  (DOID:0111397)
  • 3 papers in CRRD have been used to annotate BC052040

  • This annotation was curated on 2019-11-27 19:57:10.0 by CRRD . For more information contact us

    An association has been curated linking BC052040 and congenital dyserythropoietic anemia type Ib 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 C15orf41 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 CRRD objects have been annotated to congenital dyserythropoietic anemia type Ib  (DOID:0111397)
  • 3 papers in CRRD have been used to annotate BC052040
  • Curation Notes: ClinVar Annotator: match by term: ANEMIA, CONGENITAL DYSERYTHROPOIETIC, TYPE Ib
  • Original References(s): PMID:25741868, PMID:29885034

  • This annotation was curated on 2019-11-12 07:28:16.0 by CRRD . For more information contact us

    An association has been curated linking BC052040 and congenital dyserythropoietic anemia type Ib 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 C15orf41 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 CRRD objects have been annotated to congenital dyserythropoietic anemia type Ib  (DOID:0111397)
  • 3 papers in CRRD have been used to annotate BC052040
  • Curation Notes: ClinVar Annotator: match by term: ANEMIA, CONGENITAL DYSERYTHROPOIETIC, TYPE Ib
  • Original References(s): PMID:25741868, PMID:31191338

  • This annotation was curated on 2019-11-12 07:28:16.0 by CRRD . For more information contact us

    An association has been curated linking BC052040 and congenital dyserythropoietic anemia type Ib 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 C15orf41 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 CRRD objects have been annotated to congenital dyserythropoietic anemia type Ib  (DOID:0111397)
  • 3 papers in CRRD have been used to annotate BC052040
  • Curation Notes: ClinVar Annotator: match by term: ANEMIA, CONGENITAL DYSERYTHROPOIETIC, TYPE Ib
  • Original References(s): PMID:16643456, PMID:23716552, PMID:25741868

  • This annotation was curated on 2019-11-12 07:30:09.0 by CRRD . For more information contact us

    An association has been curated linking BC052040 and congenital dyserythropoietic anemia type Ib 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 C15orf41 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 CRRD objects have been annotated to congenital dyserythropoietic anemia type Ib  (DOID:0111397)
  • 3 papers in CRRD have been used to annotate BC052040
  • Curation Notes: ClinVar Annotator: match by term: ANEMIA, CONGENITAL DYSERYTHROPOIETIC, TYPE Ib
  • Original References(s): PMID:23716552, PMID:25741868, PMID:9220189

  • This annotation was curated on 2019-11-12 07:30:09.0 by CRRD . For more information contact us

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    RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.