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GENE - TERM ANNOTATION REPORT

16 Annotations Found.

An association has been curated linking Foxp1 and intellectual disability-severe speech delay-mild dysmorphism syndrome 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 FOXP1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to intellectual disability-severe speech delay-mild dysmorphism syndrome  (DOID:0111331)
  • 21 papers in RGD have been used to annotate Foxp1
  • Curation Notes: ClinVar Annotator: match by OMIM:613670
  • Original References(s): PMID:26647308

  • This annotation was curated on 2019-12-03 05:59:38.0 by RGD . For more information contact us

    An association has been curated linking Foxp1 and intellectual disability-severe speech delay-mild dysmorphism syndrome 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 FOXP1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to intellectual disability-severe speech delay-mild dysmorphism syndrome  (DOID:0111331)
  • 21 papers in RGD have been used to annotate Foxp1

  • This annotation was curated on 2019-12-04 19:57:08.0 by RGD . For more information contact us

    An association has been curated linking Foxp1 and intellectual disability-severe speech delay-mild dysmorphism syndrome 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 FOXP1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to intellectual disability-severe speech delay-mild dysmorphism syndrome  (DOID:0111331)
  • 21 papers in RGD have been used to annotate Foxp1
  • Curation Notes: ClinVar Annotator: match by OMIM:613670
  • Original References(s): PMID:25741868

  • This annotation was curated on 2019-12-03 06:01:43.0 by RGD . For more information contact us

    An association has been curated linking Foxp1 and intellectual disability-severe speech delay-mild dysmorphism syndrome 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 FOXP1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to intellectual disability-severe speech delay-mild dysmorphism syndrome  (DOID:0111331)
  • 21 papers in RGD have been used to annotate Foxp1
  • Curation Notes: ClinVar Annotator: match by OMIM:613670
  • Original References(s): PMID:24214399

  • This annotation was curated on 2019-12-03 05:57:07.0 by RGD . For more information contact us

    An association has been curated linking Foxp1 and intellectual disability-severe speech delay-mild dysmorphism syndrome 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 FOXP1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to intellectual disability-severe speech delay-mild dysmorphism syndrome  (DOID:0111331)
  • 21 papers in RGD have been used to annotate Foxp1
  • Curation Notes: ClinVar Annotator: match by OMIM:613670
  • Original References(s): PMID:20950788

  • This annotation was curated on 2019-12-03 05:57:42.0 by RGD . For more information contact us

    An association has been curated linking Foxp1 and intellectual disability-severe speech delay-mild dysmorphism syndrome 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 FOXP1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to intellectual disability-severe speech delay-mild dysmorphism syndrome  (DOID:0111331)
  • 21 papers in RGD have been used to annotate Foxp1
  • Curation Notes: ClinVar Annotator: match by term: Mental retardation with language impairment and with or without autistic features
  • Original References(s): PMID:23757202

  • This annotation was curated on 2019-12-03 05:59:14.0 by RGD . For more information contact us

    An association has been curated linking Foxp1 and intellectual disability-severe speech delay-mild dysmorphism syndrome 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 FOXP1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to intellectual disability-severe speech delay-mild dysmorphism syndrome  (DOID:0111331)
  • 21 papers in RGD have been used to annotate Foxp1
  • Curation Notes: ClinVar Annotator: match by OMIM:613670

  • This annotation was curated on 2019-12-03 06:01:47.0 by RGD . For more information contact us

    An association has been curated linking Foxp1 and intellectual disability-severe speech delay-mild dysmorphism syndrome 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 FOXP1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to intellectual disability-severe speech delay-mild dysmorphism syndrome  (DOID:0111331)
  • 21 papers in RGD have been used to annotate Foxp1
  • Curation Notes: ClinVar Annotator: match by term: Mental retardation with language impairment and with or without autistic features
  • Original References(s): PMID:25131622, PMID:26647308

  • This annotation was curated on 2019-12-03 05:57:09.0 by RGD . For more information contact us

    An association has been curated linking Foxp1 and intellectual disability-severe speech delay-mild dysmorphism syndrome 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 FOXP1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to intellectual disability-severe speech delay-mild dysmorphism syndrome  (DOID:0111331)
  • 21 papers in RGD have been used to annotate Foxp1
  • Curation Notes: ClinVar Annotator: match by term: Mental retardation with language impairment and with or without autistic features
  • Original References(s): PMID:20950788, PMID:26647308

  • This annotation was curated on 2019-12-03 05:57:42.0 by RGD . For more information contact us

    An association has been curated linking Foxp1 and intellectual disability-severe speech delay-mild dysmorphism syndrome 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 FOXP1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to intellectual disability-severe speech delay-mild dysmorphism syndrome  (DOID:0111331)
  • 21 papers in RGD have been used to annotate Foxp1
  • Curation Notes: ClinVar Annotator: match by term: Mental retardation with language impairment and with or without autistic features
  • Original References(s): PMID:25741868, PMID:28708303

  • This annotation was curated on 2019-12-03 05:58:37.0 by RGD . For more information contact us

    An association has been curated linking Foxp1 and intellectual disability-severe speech delay-mild dysmorphism syndrome 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 FOXP1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to intellectual disability-severe speech delay-mild dysmorphism syndrome  (DOID:0111331)
  • 21 papers in RGD have been used to annotate Foxp1
  • Curation Notes: ClinVar Annotator: match by term: Mental retardation with language impairment and with or without autistic features
  • Original References(s): PMID:12692134, PMID:20571508, PMID:20950788, PMID:21572417, PMID:22670142, PMID:24214399, PMID:24267886, PMID:25326635, PMID:25741868, PMID:25853299, PMID:26647308, PMID:27657687, PMID:27899622

  • This annotation was curated on 2019-12-03 05:55:50.0 by RGD . For more information contact us

    An association has been curated linking Foxp1 and intellectual disability-severe speech delay-mild dysmorphism syndrome 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 FOXP1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to intellectual disability-severe speech delay-mild dysmorphism syndrome  (DOID:0111331)
  • 21 papers in RGD have been used to annotate Foxp1
  • Curation Notes: ClinVar Annotator: match by term: Mental retardation with language impairment and with or without autistic features
  • Original References(s): PMID:12692134, PMID:20571508, PMID:20950788, PMID:21572417, PMID:22670142, PMID:24214399, PMID:24267886, PMID:25741868, PMID:25853299, PMID:26647308, PMID:27657687, PMID:27899622, PMID:28741757

  • This annotation was curated on 2019-12-03 06:00:28.0 by RGD . For more information contact us

    An association has been curated linking Foxp1 and intellectual disability-severe speech delay-mild dysmorphism syndrome 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 FOXP1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to intellectual disability-severe speech delay-mild dysmorphism syndrome  (DOID:0111331)
  • 21 papers in RGD have been used to annotate Foxp1
  • Curation Notes: ClinVar Annotator: match by term: Mental retardation with language impairment and with or without autistic features
  • Original References(s): PMID:25326635, PMID:25741868

  • This annotation was curated on 2019-12-03 05:56:41.0 by RGD . For more information contact us

    An association has been curated linking Foxp1 and intellectual disability-severe speech delay-mild dysmorphism syndrome 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 FOXP1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to intellectual disability-severe speech delay-mild dysmorphism syndrome  (DOID:0111331)
  • 21 papers in RGD have been used to annotate Foxp1
  • Curation Notes: ClinVar Annotator: match by term: Intellectual Disability with Language Impairment and Autistic Features
  • Original References(s): PMID:23766104, PMID:25741868

  • This annotation was curated on 2019-12-03 05:56:00.0 by RGD . For more information contact us

    An association has been curated linking Foxp1 and intellectual disability-severe speech delay-mild dysmorphism syndrome 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 FOXP1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to intellectual disability-severe speech delay-mild dysmorphism syndrome  (DOID:0111331)
  • 21 papers in RGD have been used to annotate Foxp1
  • Curation Notes: ClinVar Annotator: match by term: Intellectual Disability with Language Impairment and Autistic Features
  • Original References(s): PMID:18414213, PMID:19352412, PMID:20848658, PMID:20950788, PMID:26647308

  • This annotation was curated on 2019-12-03 05:56:02.0 by RGD . For more information contact us

    An association has been curated linking Foxp1 and intellectual disability-severe speech delay-mild dysmorphism syndrome 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 FOXP1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to intellectual disability-severe speech delay-mild dysmorphism syndrome  (DOID:0111331)
  • 21 papers in RGD have been used to annotate Foxp1
  • Curation Notes: ClinVar Annotator: match by term: Intellectual Disability with Language Impairment and Autistic Features
  • Original References(s): PMID:20848658, PMID:20950788, PMID:25741868

  • This annotation was curated on 2019-12-03 06:01:32.0 by RGD . 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.