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GENE - TERM ANNOTATION REPORT

7 Annotations Found.

An association has been curated linking LOC109610631 and non-syndromic X-linked intellectual disability ARX-related in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • 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 by association of genotype and phenotype with RGD:9684298 (Homo sapiens)
  • 2 RGD objects have been annotated to non-syndromic X-linked intellectual disability ARX-related  (DOID:0112021)
  • 0 papers in RGD have been used to annotate LOC109610631
  • Curation Notes: ClinVar Annotator: match by term: INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED 29
  • Original References(s): PMID:18414213 PMID:28492532


    • An association has been curated linking LOC109610631 and non-syndromic X-linked intellectual disability ARX-related in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • 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 by association of genotype and phenotype with RGD:8643365 (Homo sapiens)
  • 2 RGD objects have been annotated to non-syndromic X-linked intellectual disability ARX-related  (DOID:0112021)
  • 0 papers in RGD have been used to annotate LOC109610631
  • Curation Notes: ClinVar Annotator: match by term: INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED 29
  • Original References(s): PMID:17641262 PMID:18414213 PMID:21204226 PMID:25741868 PMID:28492532


    • An association has been curated linking LOC109610631 and non-syndromic X-linked intellectual disability ARX-related in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • 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 by association of genotype and phenotype with RGD:10406777 (Homo sapiens)
  • 2 RGD objects have been annotated to non-syndromic X-linked intellectual disability ARX-related  (DOID:0112021)
  • 0 papers in RGD have been used to annotate LOC109610631
  • Curation Notes: ClinVar Annotator: match by term: INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED 29
  • Original References(s): PMID:25741868 PMID:28492532


    • An association has been curated linking LOC109610631 and non-syndromic X-linked intellectual disability ARX-related in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • 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 by association of genotype and phenotype with RGD:40903574 (Homo sapiens)
  • 2 RGD objects have been annotated to non-syndromic X-linked intellectual disability ARX-related  (DOID:0112021)
  • 0 papers in RGD have been used to annotate LOC109610631
  • Curation Notes: ClinVar Annotator: match by term: INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED 29


    • An association has been curated linking LOC109610631 and non-syndromic X-linked intellectual disability ARX-related in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • 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 by association of genotype and phenotype with RGD:8562238 (Homo sapiens)
  • 2 RGD objects have been annotated to non-syndromic X-linked intellectual disability ARX-related  (DOID:0112021)
  • 0 papers in RGD have been used to annotate LOC109610631
  • Curation Notes: ClinVar Annotator: match by term: Mental retardation, X-linked 52
  • Original References(s): PMID:10353782 PMID:10398246 PMID:11889467 PMID:11971879 PMID:12116222 PMID:12376938 PMID:12376946 PMID:12376949 PMID:12640086 PMID:15151512 PMID:15200506 PMID:15850492 PMID:16078051 PMID:16235064 PMID:17331656 PMID:17480217 PMID:20506206 PMID:2080994 PMID:21204215 PMID:26029707 PMID:28492532 PMID:3177452 PMID:5008734 PMID:8826464


    • An association has been curated linking LOC109610631 and non-syndromic X-linked intellectual disability ARX-related in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • 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 by association of genotype and phenotype with RGD:13830690 (Homo sapiens)
  • 2 RGD objects have been annotated to non-syndromic X-linked intellectual disability ARX-related  (DOID:0112021)
  • 0 papers in RGD have been used to annotate LOC109610631
  • Curation Notes: ClinVar Annotator: match by term: INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED 29
  • Original References(s): PMID:16235064 PMID:17331656 PMID:20506206 PMID:21204215 PMID:26029707 PMID:28492532


    • An association has been curated linking LOC109610631 and non-syndromic X-linked intellectual disability ARX-related in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • 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 by association of genotype and phenotype with RGD:155735496 (Homo sapiens)
  • 2 RGD objects have been annotated to non-syndromic X-linked intellectual disability ARX-related  (DOID:0112021)
  • 0 papers in RGD have been used to annotate LOC109610631
  • Curation Notes: ClinVar Annotator: match by term: INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED 29
  • Original References(s): PMID:28492532


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