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GENE - TERM ANNOTATION REPORT

13 Annotations Found.

An association has been curated linking FLNA and FG Syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from OMIM Disease Annotation Pipeline
  • 2 RGD objects have been annotated to FG Syndrome 2  (DOID:9002387)
  • 23 papers in RGD have been used to annotate FLNA


    • An association has been curated linking FLNA and FG Syndrome 2 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:127289087 (Homo sapiens)
  • 2 RGD objects have been annotated to FG Syndrome 2  (DOID:9002387)
  • 23 papers in RGD have been used to annotate FLNA
  • Curation Notes: ClinVar Annotator: match by term: FG syndrome 2
  • Original References(s): PMID:25741868 PMID:28492532 PMID:29720203


    • An association has been curated linking FLNA and FG Syndrome 2 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:8640665 (Homo sapiens)
  • 2 RGD objects have been annotated to FG Syndrome 2  (DOID:9002387)
  • 23 papers in RGD have been used to annotate FLNA
  • Curation Notes: ClinVar Annotator: match by term: FG syndrome 2
  • Original References(s): PMID:10982489 PMID:12612583 PMID:16417552 PMID:16822260 PMID:18414213 PMID:22522697 PMID:25741868 PMID:26467025 PMID:28492532


    • An association has been curated linking FLNA and FG Syndrome 2 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:153346416 (Homo sapiens)
  • 2 RGD objects have been annotated to FG Syndrome 2  (DOID:9002387)
  • 23 papers in RGD have been used to annotate FLNA
  • Curation Notes: ClinVar Annotator: match by term: FG syndrome 2
  • Original References(s): PMID:25741868 PMID:30089473


    • An association has been curated linking FLNA and FG Syndrome 2 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:12843222 (Homo sapiens)
  • 2 RGD objects have been annotated to FG Syndrome 2  (DOID:9002387)
  • 23 papers in RGD have been used to annotate FLNA
  • Curation Notes: ClinVar Annotator: match by term: FG syndrome 2
  • Original References(s): PMID:25741868 PMID:28492532 PMID:35000503


    • An association has been curated linking FLNA and FG Syndrome 2 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:10052763|RGD:10409580|RGD:10409931|RGD:10410462|RGD:10410843|RGD:126772256|RGD:12842483|RGD:12889006|RGD:13213543|RGD:13498329|RGD:13609590|RGD:13827542|RGD:13829113|RGD:13829208|RGD:13829446|RGD:14398984|RGD:15154784|RGD:156056653|RGD:25317152 (Homo sapiens) & RGD:10052763|RGD:10409580|RGD:10409931|RGD:10410462|RGD:10410843|RGD:126772256|RGD:12842483|RGD:12889006|RGD:13213543|RGD:13498329|RGD:13609590|RGD:13827542|RGD:13829113|RGD:13829208|RGD:13829446|RGD:14398984|RGD:15154784|RGD:156056653|RGD:25317152 (Homo sapiens) & RGD:10052763|RGD:10409580|RGD:10409931|RGD:10410462|RGD:10410843|RGD:126772256|RGD:12842483|RGD:12889006|RGD:13213543|RGD:13498329|RGD:13609590|RGD:13827542|RGD:13829113|RGD:13829208|RGD:13829446|RGD:14398984|RGD:15154784|RGD:156056653|RGD:25317152 (Homo sapiens) & RGD:10052763|RGD:10409580|RGD:10409931|RGD:10410462|RGD:10410843|RGD:126772256|RGD:12842483|RGD:12889006|RGD:13213543|RGD:13498329|RGD:13609590|RGD:13827542|RGD:13829113|RGD:13829208|RGD:13829446|RGD:14398984|RGD:15154784|RGD:156056653|RGD:25317152 (Homo sapiens) & RGD:10052763|RGD:10409580|RGD:10409931|RGD:10410462|RGD:10410843|RGD:126772256|RGD:12842483|RGD:12889006|RGD:13213543|RGD:13498329|RGD:13609590|RGD:13827542|RGD:13829113|RGD:13829208|RGD:13829446|RGD:14398984|RGD:15154784|RGD:156056653|RGD:25317152 (Homo sapiens) & RGD:10052763|RGD:10409580|RGD:10409931|RGD:10410462|RGD:10410843|RGD:126772256|RGD:12842483|RGD:12889006|RGD:13213543|RGD:13498329|RGD:13609590|RGD:13827542|RGD:13829113|RGD:13829208|RGD:13829446|RGD:14398984|RGD:15154784|RGD:156056653|RGD:25317152 (Homo sapiens) & RGD:10052763|RGD:10409580|RGD:10409931|RGD:10410462|RGD:10410843|RGD:126772256|RGD:12842483|RGD:12889006|RGD:13213543|RGD:13498329|RGD:13609590|RGD:13827542|RGD:13829113|RGD:13829208|RGD:13829446|RGD:14398984|RGD:15154784|RGD:156056653|RGD:25317152 (Homo sapiens) & RGD:10052763|RGD:10409580|RGD:10409931|RGD:10410462|RGD:10410843|RGD:126772256|RGD:12842483|RGD:12889006|RGD:13213543|RGD:13498329|RGD:13609590|RGD:13827542|RGD:13829113|RGD:13829208|RGD:13829446|RGD:14398984|RGD:15154784|RGD:156056653|RGD:25317152 (Homo sapiens) & RGD:10052763|RGD:10409580|RGD:10409931|RGD:10410462|RGD:10410843|RGD:126772256|RGD:12842483|RGD:12889006|RGD:13213543|RGD:13498329|RGD:13609590|RGD:13827542|RGD:13829113|RGD:13829208|RGD:13829446|RGD:14398984|RGD:15154784|RGD:156056653|RGD:25317152 (Homo sapiens) & RGD:10052763|RGD:10409580|RGD:10409931|RGD:10410462|RGD:10410843|RGD:126772256|RGD:12842483|RGD:12889006|RGD:13213543|RGD:13498329|RGD:13609590|RGD:13827542|RGD:13829113|RGD:13829208|RGD:13829446|RGD:14398984|RGD:15154784|RGD:156056653|RGD:25317152 (Homo sapiens) & RGD:10052763|RGD:10409580|RGD:10409931|RGD:10410462|RGD:10410843|RGD:126772256|RGD:12842483|RGD:12889006|RGD:13213543|RGD:13498329|RGD:13609590|RGD:13827542|RGD:13829113|RGD:13829208|RGD:13829446|RGD:14398984|RGD:15154784|RGD:156056653|RGD:25317152 (Homo sapiens) & RGD:10052763|RGD:10409580|RGD:10409931|RGD:10410462|RGD:10410843|RGD:126772256|RGD:12842483|RGD:12889006|RGD:13213543|RGD:13498329|RGD:13609590|RGD:13827542|RGD:13829113|RGD:13829208|RGD:13829446|RGD:14398984|RGD:15154784|RGD:156056653|RGD:25317152 (Homo sapiens) & RGD:10052763|RGD:10409580|RGD:10409931|RGD:10410462|RGD:10410843|RGD:126772256|RGD:12842483|RGD:12889006|RGD:13213543|RGD:13498329|RGD:13609590|RGD:13827542|RGD:13829113|RGD:13829208|RGD:13829446|RGD:14398984|RGD:15154784|RGD:156056653|RGD:25317152 (Homo sapiens) & RGD:10052763|RGD:10409580|RGD:10409931|RGD:10410462|RGD:10410843|RGD:126772256|RGD:12842483|RGD:12889006|RGD:13213543|RGD:13498329|RGD:13609590|RGD:13827542|RGD:13829113|RGD:13829208|RGD:13829446|RGD:14398984|RGD:15154784|RGD:156056653|RGD:25317152 (Homo sapiens) & RGD:10052763|RGD:10409580|RGD:10409931|RGD:10410462|RGD:10410843|RGD:126772256|RGD:12842483|RGD:12889006|RGD:13213543|RGD:13498329|RGD:13609590|RGD:13827542|RGD:13829113|RGD:13829208|RGD:13829446|RGD:14398984|RGD:15154784|RGD:156056653|RGD:25317152 (Homo sapiens) & RGD:10052763|RGD:10409580|RGD:10409931|RGD:10410462|RGD:10410843|RGD:126772256|RGD:12842483|RGD:12889006|RGD:13213543|RGD:13498329|RGD:13609590|RGD:13827542|RGD:13829113|RGD:13829208|RGD:13829446|RGD:14398984|RGD:15154784|RGD:156056653|RGD:25317152 (Homo sapiens) & RGD:10052763|RGD:10409580|RGD:10409931|RGD:10410462|RGD:10410843|RGD:126772256|RGD:12842483|RGD:12889006|RGD:13213543|RGD:13498329|RGD:13609590|RGD:13827542|RGD:13829113|RGD:13829208|RGD:13829446|RGD:14398984|RGD:15154784|RGD:156056653|RGD:25317152 (Homo sapiens) & RGD:10052763|RGD:10409580|RGD:10409931|RGD:10410462|RGD:10410843|RGD:126772256|RGD:12842483|RGD:12889006|RGD:13213543|RGD:13498329|RGD:13609590|RGD:13827542|RGD:13829113|RGD:13829208|RGD:13829446|RGD:14398984|RGD:15154784|RGD:156056653|RGD:25317152 (Homo sapiens) & RGD:10052763|RGD:10409580|RGD:10409931|RGD:10410462|RGD:10410843|RGD:126772256|RGD:12842483|RGD:12889006|RGD:13213543|RGD:13498329|RGD:13609590|RGD:13827542|RGD:13829113|RGD:13829208|RGD:13829446|RGD:14398984|RGD:15154784|RGD:156056653|RGD:25317152 (Homo sapiens)
  • 2 RGD objects have been annotated to FG Syndrome 2  (DOID:9002387)
  • 23 papers in RGD have been used to annotate FLNA
  • Curation Notes: ClinVar Annotator: match by term: FG syndrome 2
  • Original References(s): PMID:25741868 PMID:28492532


    • An association has been curated linking FLNA and FG Syndrome 2 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:8562714 (Homo sapiens)
  • 2 RGD objects have been annotated to FG Syndrome 2  (DOID:9002387)
  • 23 papers in RGD have been used to annotate FLNA
  • Curation Notes: ClinVar Annotator: match by term: FG syndrome 2
  • Original References(s): PMID:16299064 PMID:17632775 PMID:25167861 PMID:25741868 PMID:28133863 PMID:28492532


    • An association has been curated linking FLNA and FG Syndrome 2 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:8640670|RGD:8659571|RGD:8659578 (Homo sapiens) & RGD:8640670|RGD:8659571|RGD:8659578 (Homo sapiens) & RGD:8640670|RGD:8659571|RGD:8659578 (Homo sapiens)
  • 2 RGD objects have been annotated to FG Syndrome 2  (DOID:9002387)
  • 23 papers in RGD have been used to annotate FLNA
  • Curation Notes: ClinVar Annotator: match by term: FG syndrome 2
  • Original References(s): PMID:18414213 PMID:25741868 PMID:28492532


    • An association has been curated linking FLNA and FG Syndrome 2 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:13211378|RGD:13829993 (Homo sapiens) & RGD:13211378|RGD:13829993 (Homo sapiens)
  • 2 RGD objects have been annotated to FG Syndrome 2  (DOID:9002387)
  • 23 papers in RGD have been used to annotate FLNA
  • Curation Notes: ClinVar Annotator: match by term: FG syndrome 2
  • Original References(s): PMID:25741868 PMID:28492532 PMID:30986657


    • An association has been curated linking FLNA and FG Syndrome 2 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:13497704|RGD:14702988 (Homo sapiens) & RGD:13497704|RGD:14702988 (Homo sapiens)
  • 2 RGD objects have been annotated to FG Syndrome 2  (DOID:9002387)
  • 23 papers in RGD have been used to annotate FLNA
  • Curation Notes: ClinVar Annotator: match by term: FG syndrome 2
  • Original References(s): PMID:28492532


    • An association has been curated linking FLNA and FG Syndrome 2 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:39456676|RGD:39456760 (Homo sapiens) & RGD:39456676|RGD:39456760 (Homo sapiens)
  • 2 RGD objects have been annotated to FG Syndrome 2  (DOID:9002387)
  • 23 papers in RGD have been used to annotate FLNA
  • Curation Notes: ClinVar Annotator: match by term: FG syndrome 2


    • An association has been curated linking FLNA and FG Syndrome 2 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:126726495|RGD:13704786|RGD:150534634|RGD:401917968 (Homo sapiens) & RGD:126726495|RGD:13704786|RGD:150534634|RGD:401917968 (Homo sapiens) & RGD:126726495|RGD:13704786|RGD:150534634|RGD:401917968 (Homo sapiens) & RGD:126726495|RGD:13704786|RGD:150534634|RGD:401917968 (Homo sapiens)
  • 2 RGD objects have been annotated to FG Syndrome 2  (DOID:9002387)
  • 23 papers in RGD have been used to annotate FLNA
  • Curation Notes: ClinVar Annotator: match by term: FG syndrome 2
  • Original References(s): PMID:25741868


    • An association has been curated linking FLNA and FG Syndrome 2 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:10411616|RGD:8640684|RGD:8640694 (Homo sapiens) & RGD:10411616|RGD:8640684|RGD:8640694 (Homo sapiens) & RGD:10411616|RGD:8640684|RGD:8640694 (Homo sapiens)
  • 2 RGD objects have been annotated to FG Syndrome 2  (DOID:9002387)
  • 23 papers in RGD have been used to annotate FLNA
  • Curation Notes: ClinVar Annotator: match by term: FG syndrome 2
  • Original References(s): PMID:25741868 PMID:26467025 PMID:28492532


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