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GENE - TERM ANNOTATION REPORT

18 Annotations Found.

An association has been curated linking FGD1 and Aarskog syndrome in Homo sapiens.        

  • The association was inferred from experiment (EXP)
    		•  
  • The annotation was made from RGD automated import pipeline for CTD gene-to-disease annotations
  • 2 RGD objects have been annotated to Aarskog syndrome  (DOID:0111824)
  • 11 papers in RGD have been used to annotate FGD1
  • Curation Notes: CTD Direct Evidence: marker/mechanism
  • Original References(s): PMID:7954831 PMID:10930571 PMID:11093277 PMID:14560308 PMID:15327482 PMID:17152066


    • An association has been curated linking FGD1 and Aarskog syndrome 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:8561948 (Homo sapiens)
  • 2 RGD objects have been annotated to Aarskog syndrome  (DOID:0111824)
  • 11 papers in RGD have been used to annotate FGD1
  • Curation Notes: ClinVar Annotator: match by term: Aarskog syndrome
  • Original References(s): PMID:15809997 PMID:16688726


    • An association has been curated linking FGD1 and Aarskog syndrome 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:13506485 (Homo sapiens)
  • 2 RGD objects have been annotated to Aarskog syndrome  (DOID:0111824)
  • 11 papers in RGD have been used to annotate FGD1
  • Curation Notes: ClinVar Annotator: match by term: Aarskog syndrome
  • Original References(s): PMID:29276006


    • An association has been curated linking FGD1 and Aarskog syndrome 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:8561943 (Homo sapiens)
  • 2 RGD objects have been annotated to Aarskog syndrome  (DOID:0111824)
  • 11 papers in RGD have been used to annotate FGD1
  • Curation Notes: ClinVar Annotator: match by term: Aarskog syndrome
  • Original References(s): PMID:11093277


    • An association has been curated linking FGD1 and Aarskog syndrome 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:8561940 (Homo sapiens)
  • 2 RGD objects have been annotated to Aarskog syndrome  (DOID:0111824)
  • 11 papers in RGD have been used to annotate FGD1
  • Curation Notes: ClinVar Annotator: match by term: Aarskog syndrome
  • Original References(s): PMID:7954831


    • An association has been curated linking FGD1 and Aarskog syndrome 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:8561944 (Homo sapiens)
  • 2 RGD objects have been annotated to Aarskog syndrome  (DOID:0111824)
  • 11 papers in RGD have been used to annotate FGD1
  • Curation Notes: ClinVar Annotator: match by term: Aarskog syndrome
  • Original References(s): PMID:11940089 PMID:25741868 PMID:28492532


    • An association has been curated linking FGD1 and Aarskog syndrome 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:8561947 (Homo sapiens)
  • 2 RGD objects have been annotated to Aarskog syndrome  (DOID:0111824)
  • 11 papers in RGD have been used to annotate FGD1
  • Curation Notes: ClinVar Annotator: match by term: Aarskog syndrome
  • Original References(s): PMID:16353258


    • An association has been curated linking FGD1 and Aarskog syndrome 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:8568039 (Homo sapiens)
  • 2 RGD objects have been annotated to Aarskog syndrome  (DOID:0111824)
  • 11 papers in RGD have been used to annotate FGD1
  • Curation Notes: ClinVar Annotator: match by term: Aarskog syndrome
  • Original References(s): PMID:20082460 PMID:25741868


    • An association has been curated linking FGD1 and Aarskog syndrome 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:12739036 (Homo sapiens)
  • 2 RGD objects have been annotated to Aarskog syndrome  (DOID:0111824)
  • 11 papers in RGD have been used to annotate FGD1
  • Curation Notes: ClinVar Annotator: match by term: Aarskog syndrome
  • Original References(s): PMID:20082460 PMID:21739585 PMID:23211637 PMID:25046119 PMID:25741868 PMID:26029706 PMID:27959697 PMID:28492532


    • An association has been curated linking FGD1 and Aarskog syndrome 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:8561941 (Homo sapiens)
  • 2 RGD objects have been annotated to Aarskog syndrome  (DOID:0111824)
  • 11 papers in RGD have been used to annotate FGD1
  • Curation Notes: ClinVar Annotator: match by term: Aarskog syndrome
  • Original References(s): PMID:10930571 PMID:28492532


    • An association has been curated linking FGD1 and Aarskog syndrome 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:10048512 (Homo sapiens)
  • 2 RGD objects have been annotated to Aarskog syndrome  (DOID:0111824)
  • 11 papers in RGD have been used to annotate FGD1
  • Curation Notes: ClinVar Annotator: match by term: Aarskog syndrome
  • Original References(s): PMID:14560308 PMID:21739585 PMID:23211637 PMID:25046119 PMID:25741868 PMID:26029706 PMID:28492532 PMID:29276006


    • An association has been curated linking FGD1 and Aarskog syndrome 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:8561942 (Homo sapiens)
  • 2 RGD objects have been annotated to Aarskog syndrome  (DOID:0111824)
  • 11 papers in RGD have been used to annotate FGD1
  • Curation Notes: ClinVar Annotator: match by term: Aarskog syndrome
  • Original References(s): PMID:11093277 PMID:28492532


    • An association has been curated linking FGD1 and Aarskog syndrome 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:8561946 (Homo sapiens)
  • 2 RGD objects have been annotated to Aarskog syndrome  (DOID:0111824)
  • 11 papers in RGD have been used to annotate FGD1
  • Curation Notes: ClinVar Annotator: match by term: Aarskog syndrome
  • Original References(s): PMID:15809997 PMID:28492532


    • An association has been curated linking FGD1 and Aarskog syndrome 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:8561949 (Homo sapiens)
  • 2 RGD objects have been annotated to Aarskog syndrome  (DOID:0111824)
  • 11 papers in RGD have been used to annotate FGD1
  • Curation Notes: ClinVar Annotator: match by term: Aarskog syndrome
  • Original References(s): PMID:17152066 PMID:21739585 PMID:23211637 PMID:25046119 PMID:26029706 PMID:28492532 PMID:4146757


    • An association has been curated linking FGD1 and Aarskog syndrome 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:13532839|RGD:8561950 (Homo sapiens) & RGD:13532839|RGD:8561950 (Homo sapiens)
  • 2 RGD objects have been annotated to Aarskog syndrome  (DOID:0111824)
  • 11 papers in RGD have been used to annotate FGD1
  • Curation Notes: ClinVar Annotator: match by term: Aarskog syndrome
  • Original References(s): PMID:17847065


    • An association has been curated linking FGD1 and Aarskog syndrome 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:11643839|RGD:150556334|RGD:243059002|RGD:243059084|RGD:8642008 (Homo sapiens) & RGD:11643839|RGD:150556334|RGD:243059002|RGD:243059084|RGD:8642008 (Homo sapiens) & RGD:11643839|RGD:150556334|RGD:243059002|RGD:243059084|RGD:8642008 (Homo sapiens) & RGD:11643839|RGD:150556334|RGD:243059002|RGD:243059084|RGD:8642008 (Homo sapiens) & RGD:11643839|RGD:150556334|RGD:243059002|RGD:243059084|RGD:8642008 (Homo sapiens)
  • 2 RGD objects have been annotated to Aarskog syndrome  (DOID:0111824)
  • 11 papers in RGD have been used to annotate FGD1
  • Curation Notes: ClinVar Annotator: match by term: Aarskog syndrome
  • Original References(s): PMID:25741868 PMID:28492532


    • An association has been curated linking FGD1 and Aarskog syndrome 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:11051461|RGD:11545851|RGD:126729812|RGD:127243935|RGD:13703605|RGD:13703607|RGD:13703609|RGD:13703612|RGD:13704254|RGD:13706230|RGD:13781921|RGD:15040342|RGD:15040349|RGD:152977881|RGD:153346572|RGD:155266091|RGD:155268007|RGD:155643784|RGD:155800976|RGD:21075095|RGD:243050572|RGD:243055715|RGD:243059000|RGD:243059001|RGD:243059003|RGD:243059004|RGD:26902671|RGD:38463410|RGD:401721331|RGD:401828530|RGD:401828533|RGD:401828551|RGD:40815109|RGD:8641992 (Homo sapiens) & RGD:11051461|RGD:11545851|RGD:126729812|RGD:127243935|RGD:13703605|RGD:13703607|RGD:13703609|RGD:13703612|RGD:13704254|RGD:13706230|RGD:13781921|RGD:15040342|RGD:15040349|RGD:152977881|RGD:153346572|RGD:155266091|RGD:155268007|RGD:155643784|RGD:155800976|RGD:21075095|RGD:243050572|RGD:243055715|RGD:243059000|RGD:243059001|RGD:243059003|RGD:243059004|RGD:26902671|RGD:38463410|RGD:401721331|RGD:401828530|RGD:401828533|RGD:401828551|RGD:40815109|RGD:8641992 (Homo sapiens) & RGD:11051461|RGD:11545851|RGD:126729812|RGD:127243935|RGD:13703605|RGD:13703607|RGD:13703609|RGD:13703612|RGD:13704254|RGD:13706230|RGD:13781921|RGD:15040342|RGD:15040349|RGD:152977881|RGD:153346572|RGD:155266091|RGD:155268007|RGD:155643784|RGD:155800976|RGD:21075095|RGD:243050572|RGD:243055715|RGD:243059000|RGD:243059001|RGD:243059003|RGD:243059004|RGD:26902671|RGD:38463410|RGD:401721331|RGD:401828530|RGD:401828533|RGD:401828551|RGD:40815109|RGD:8641992 (Homo sapiens) & RGD:11051461|RGD:11545851|RGD:126729812|RGD:127243935|RGD:13703605|RGD:13703607|RGD:13703609|RGD:13703612|RGD:13704254|RGD:13706230|RGD:13781921|RGD:15040342|RGD:15040349|RGD:152977881|RGD:153346572|RGD:155266091|RGD:155268007|RGD:155643784|RGD:155800976|RGD:21075095|RGD:243050572|RGD:243055715|RGD:243059000|RGD:243059001|RGD:243059003|RGD:243059004|RGD:26902671|RGD:38463410|RGD:401721331|RGD:401828530|RGD:401828533|RGD:401828551|RGD:40815109|RGD:8641992 (Homo sapiens) & RGD:11051461|RGD:11545851|RGD:126729812|RGD:127243935|RGD:13703605|RGD:13703607|RGD:13703609|RGD:13703612|RGD:13704254|RGD:13706230|RGD:13781921|RGD:15040342|RGD:15040349|RGD:152977881|RGD:153346572|RGD:155266091|RGD:155268007|RGD:155643784|RGD:155800976|RGD:21075095|RGD:243050572|RGD:243055715|RGD:243059000|RGD:243059001|RGD:243059003|RGD:243059004|RGD:26902671|RGD:38463410|RGD:401721331|RGD:401828530|RGD:401828533|RGD:401828551|RGD:40815109|RGD:8641992 (Homo sapiens) & RGD:11051461|RGD:11545851|RGD:126729812|RGD:127243935|RGD:13703605|RGD:13703607|RGD:13703609|RGD:13703612|RGD:13704254|RGD:13706230|RGD:13781921|RGD:15040342|RGD:15040349|RGD:152977881|RGD:153346572|RGD:155266091|RGD:155268007|RGD:155643784|RGD:155800976|RGD:21075095|RGD:243050572|RGD:243055715|RGD:243059000|RGD:243059001|RGD:243059003|RGD:243059004|RGD:26902671|RGD:38463410|RGD:401721331|RGD:401828530|RGD:401828533|RGD:401828551|RGD:40815109|RGD:8641992 (Homo sapiens) & RGD:11051461|RGD:11545851|RGD:126729812|RGD:127243935|RGD:13703605|RGD:13703607|RGD:13703609|RGD:13703612|RGD:13704254|RGD:13706230|RGD:13781921|RGD:15040342|RGD:15040349|RGD:152977881|RGD:153346572|RGD:155266091|RGD:155268007|RGD:155643784|RGD:155800976|RGD:21075095|RGD:243050572|RGD:243055715|RGD:243059000|RGD:243059001|RGD:243059003|RGD:243059004|RGD:26902671|RGD:38463410|RGD:401721331|RGD:401828530|RGD:401828533|RGD:401828551|RGD:40815109|RGD:8641992 (Homo sapiens) & RGD:11051461|RGD:11545851|RGD:126729812|RGD:127243935|RGD:13703605|RGD:13703607|RGD:13703609|RGD:13703612|RGD:13704254|RGD:13706230|RGD:13781921|RGD:15040342|RGD:15040349|RGD:152977881|RGD:153346572|RGD:155266091|RGD:155268007|RGD:155643784|RGD:155800976|RGD:21075095|RGD:243050572|RGD:243055715|RGD:243059000|RGD:243059001|RGD:243059003|RGD:243059004|RGD:26902671|RGD:38463410|RGD:401721331|RGD:401828530|RGD:401828533|RGD:401828551|RGD:40815109|RGD:8641992 (Homo sapiens) & RGD:11051461|RGD:11545851|RGD:126729812|RGD:127243935|RGD:13703605|RGD:13703607|RGD:13703609|RGD:13703612|RGD:13704254|RGD:13706230|RGD:13781921|RGD:15040342|RGD:15040349|RGD:152977881|RGD:153346572|RGD:155266091|RGD:155268007|RGD:155643784|RGD:155800976|RGD:21075095|RGD:243050572|RGD:243055715|RGD:243059000|RGD:243059001|RGD:243059003|RGD:243059004|RGD:26902671|RGD:38463410|RGD:401721331|RGD:401828530|RGD:401828533|RGD:401828551|RGD:40815109|RGD:8641992 (Homo sapiens) & RGD:11051461|RGD:11545851|RGD:126729812|RGD:127243935|RGD:13703605|RGD:13703607|RGD:13703609|RGD:13703612|RGD:13704254|RGD:13706230|RGD:13781921|RGD:15040342|RGD:15040349|RGD:152977881|RGD:153346572|RGD:155266091|RGD:155268007|RGD:155643784|RGD:155800976|RGD:21075095|RGD:243050572|RGD:243055715|RGD:243059000|RGD:243059001|RGD:243059003|RGD:243059004|RGD:26902671|RGD:38463410|RGD:401721331|RGD:401828530|RGD:401828533|RGD:401828551|RGD:40815109|RGD:8641992 (Homo sapiens) & RGD:11051461|RGD:11545851|RGD:126729812|RGD:127243935|RGD:13703605|RGD:13703607|RGD:13703609|RGD:13703612|RGD:13704254|RGD:13706230|RGD:13781921|RGD:15040342|RGD:15040349|RGD:152977881|RGD:153346572|RGD:155266091|RGD:155268007|RGD:155643784|RGD:155800976|RGD:21075095|RGD:243050572|RGD:243055715|RGD:243059000|RGD:243059001|RGD:243059003|RGD:243059004|RGD:26902671|RGD:38463410|RGD:401721331|RGD:401828530|RGD:401828533|RGD:401828551|RGD:40815109|RGD:8641992 (Homo sapiens) & RGD:11051461|RGD:11545851|RGD:126729812|RGD:127243935|RGD:13703605|RGD:13703607|RGD:13703609|RGD:13703612|RGD:13704254|RGD:13706230|RGD:13781921|RGD:15040342|RGD:15040349|RGD:152977881|RGD:153346572|RGD:155266091|RGD:155268007|RGD:155643784|RGD:155800976|RGD:21075095|RGD:243050572|RGD:243055715|RGD:243059000|RGD:243059001|RGD:243059003|RGD:243059004|RGD:26902671|RGD:38463410|RGD:401721331|RGD:401828530|RGD:401828533|RGD:401828551|RGD:40815109|RGD:8641992 (Homo sapiens) & RGD:11051461|RGD:11545851|RGD:126729812|RGD:127243935|RGD:13703605|RGD:13703607|RGD:13703609|RGD:13703612|RGD:13704254|RGD:13706230|RGD:13781921|RGD:15040342|RGD:15040349|RGD:152977881|RGD:153346572|RGD:155266091|RGD:155268007|RGD:155643784|RGD:155800976|RGD:21075095|RGD:243050572|RGD:243055715|RGD:243059000|RGD:243059001|RGD:243059003|RGD:243059004|RGD:26902671|RGD:38463410|RGD:401721331|RGD:401828530|RGD:401828533|RGD:401828551|RGD:40815109|RGD:8641992 (Homo sapiens) & RGD:11051461|RGD:11545851|RGD:126729812|RGD:127243935|RGD:13703605|RGD:13703607|RGD:13703609|RGD:13703612|RGD:13704254|RGD:13706230|RGD:13781921|RGD:15040342|RGD:15040349|RGD:152977881|RGD:153346572|RGD:155266091|RGD:155268007|RGD:155643784|RGD:155800976|RGD:21075095|RGD:243050572|RGD:243055715|RGD:243059000|RGD:243059001|RGD:243059003|RGD:243059004|RGD:26902671|RGD:38463410|RGD:401721331|RGD:401828530|RGD:401828533|RGD:401828551|RGD:40815109|RGD:8641992 (Homo sapiens) & RGD:11051461|RGD:11545851|RGD:126729812|RGD:127243935|RGD:13703605|RGD:13703607|RGD:13703609|RGD:13703612|RGD:13704254|RGD:13706230|RGD:13781921|RGD:15040342|RGD:15040349|RGD:152977881|RGD:153346572|RGD:155266091|RGD:155268007|RGD:155643784|RGD:155800976|RGD:21075095|RGD:243050572|RGD:243055715|RGD:243059000|RGD:243059001|RGD:243059003|RGD:243059004|RGD:26902671|RGD:38463410|RGD:401721331|RGD:401828530|RGD:401828533|RGD:401828551|RGD:40815109|RGD:8641992 (Homo sapiens) & RGD:11051461|RGD:11545851|RGD:126729812|RGD:127243935|RGD:13703605|RGD:13703607|RGD:13703609|RGD:13703612|RGD:13704254|RGD:13706230|RGD:13781921|RGD:15040342|RGD:15040349|RGD:152977881|RGD:153346572|RGD:155266091|RGD:155268007|RGD:155643784|RGD:155800976|RGD:21075095|RGD:243050572|RGD:243055715|RGD:243059000|RGD:243059001|RGD:243059003|RGD:243059004|RGD:26902671|RGD:38463410|RGD:401721331|RGD:401828530|RGD:401828533|RGD:401828551|RGD:40815109|RGD:8641992 (Homo sapiens) & RGD:11051461|RGD:11545851|RGD:126729812|RGD:127243935|RGD:13703605|RGD:13703607|RGD:13703609|RGD:13703612|RGD:13704254|RGD:13706230|RGD:13781921|RGD:15040342|RGD:15040349|RGD:152977881|RGD:153346572|RGD:155266091|RGD:155268007|RGD:155643784|RGD:155800976|RGD:21075095|RGD:243050572|RGD:243055715|RGD:243059000|RGD:243059001|RGD:243059003|RGD:243059004|RGD:26902671|RGD:38463410|RGD:401721331|RGD:401828530|RGD:401828533|RGD:401828551|RGD:40815109|RGD:8641992 (Homo sapiens) & RGD:11051461|RGD:11545851|RGD:126729812|RGD:127243935|RGD:13703605|RGD:13703607|RGD:13703609|RGD:13703612|RGD:13704254|RGD:13706230|RGD:13781921|RGD:15040342|RGD:15040349|RGD:152977881|RGD:153346572|RGD:155266091|RGD:155268007|RGD:155643784|RGD:155800976|RGD:21075095|RGD:243050572|RGD:243055715|RGD:243059000|RGD:243059001|RGD:243059003|RGD:243059004|RGD:26902671|RGD:38463410|RGD:401721331|RGD:401828530|RGD:401828533|RGD:401828551|RGD:40815109|RGD:8641992 (Homo sapiens) & RGD:11051461|RGD:11545851|RGD:126729812|RGD:127243935|RGD:13703605|RGD:13703607|RGD:13703609|RGD:13703612|RGD:13704254|RGD:13706230|RGD:13781921|RGD:15040342|RGD:15040349|RGD:152977881|RGD:153346572|RGD:155266091|RGD:155268007|RGD:155643784|RGD:155800976|RGD:21075095|RGD:243050572|RGD:243055715|RGD:243059000|RGD:243059001|RGD:243059003|RGD:243059004|RGD:26902671|RGD:38463410|RGD:401721331|RGD:401828530|RGD:401828533|RGD:401828551|RGD:40815109|RGD:8641992 (Homo sapiens) & RGD:11051461|RGD:11545851|RGD:126729812|RGD:127243935|RGD:13703605|RGD:13703607|RGD:13703609|RGD:13703612|RGD:13704254|RGD:13706230|RGD:13781921|RGD:15040342|RGD:15040349|RGD:152977881|RGD:153346572|RGD:155266091|RGD:155268007|RGD:155643784|RGD:155800976|RGD:21075095|RGD:243050572|RGD:243055715|RGD:243059000|RGD:243059001|RGD:243059003|RGD:243059004|RGD:26902671|RGD:38463410|RGD:401721331|RGD:401828530|RGD:401828533|RGD:401828551|RGD:40815109|RGD:8641992 (Homo sapiens) & RGD:11051461|RGD:11545851|RGD:126729812|RGD:127243935|RGD:13703605|RGD:13703607|RGD:13703609|RGD:13703612|RGD:13704254|RGD:13706230|RGD:13781921|RGD:15040342|RGD:15040349|RGD:152977881|RGD:153346572|RGD:155266091|RGD:155268007|RGD:155643784|RGD:155800976|RGD:21075095|RGD:243050572|RGD:243055715|RGD:243059000|RGD:243059001|RGD:243059003|RGD:243059004|RGD:26902671|RGD:38463410|RGD:401721331|RGD:401828530|RGD:401828533|RGD:401828551|RGD:40815109|RGD:8641992 (Homo sapiens) & RGD:11051461|RGD:11545851|RGD:126729812|RGD:127243935|RGD:13703605|RGD:13703607|RGD:13703609|RGD:13703612|RGD:13704254|RGD:13706230|RGD:13781921|RGD:15040342|RGD:15040349|RGD:152977881|RGD:153346572|RGD:155266091|RGD:155268007|RGD:155643784|RGD:155800976|RGD:21075095|RGD:243050572|RGD:243055715|RGD:243059000|RGD:243059001|RGD:243059003|RGD:243059004|RGD:26902671|RGD:38463410|RGD:401721331|RGD:401828530|RGD:401828533|RGD:401828551|RGD:40815109|RGD:8641992 (Homo sapiens) & RGD:11051461|RGD:11545851|RGD:126729812|RGD:127243935|RGD:13703605|RGD:13703607|RGD:13703609|RGD:13703612|RGD:13704254|RGD:13706230|RGD:13781921|RGD:15040342|RGD:15040349|RGD:152977881|RGD:153346572|RGD:155266091|RGD:155268007|RGD:155643784|RGD:155800976|RGD:21075095|RGD:243050572|RGD:243055715|RGD:243059000|RGD:243059001|RGD:243059003|RGD:243059004|RGD:26902671|RGD:38463410|RGD:401721331|RGD:401828530|RGD:401828533|RGD:401828551|RGD:40815109|RGD:8641992 (Homo sapiens) & RGD:11051461|RGD:11545851|RGD:126729812|RGD:127243935|RGD:13703605|RGD:13703607|RGD:13703609|RGD:13703612|RGD:13704254|RGD:13706230|RGD:13781921|RGD:15040342|RGD:15040349|RGD:152977881|RGD:153346572|RGD:155266091|RGD:155268007|RGD:155643784|RGD:155800976|RGD:21075095|RGD:243050572|RGD:243055715|RGD:243059000|RGD:243059001|RGD:243059003|RGD:243059004|RGD:26902671|RGD:38463410|RGD:401721331|RGD:401828530|RGD:401828533|RGD:401828551|RGD:40815109|RGD:8641992 (Homo sapiens) & RGD:11051461|RGD:11545851|RGD:126729812|RGD:127243935|RGD:13703605|RGD:13703607|RGD:13703609|RGD:13703612|RGD:13704254|RGD:13706230|RGD:13781921|RGD:15040342|RGD:15040349|RGD:152977881|RGD:153346572|RGD:155266091|RGD:155268007|RGD:155643784|RGD:155800976|RGD:21075095|RGD:243050572|RGD:243055715|RGD:243059000|RGD:243059001|RGD:243059003|RGD:243059004|RGD:26902671|RGD:38463410|RGD:401721331|RGD:401828530|RGD:401828533|RGD:401828551|RGD:40815109|RGD:8641992 (Homo sapiens) & RGD:11051461|RGD:11545851|RGD:126729812|RGD:127243935|RGD:13703605|RGD:13703607|RGD:13703609|RGD:13703612|RGD:13704254|RGD:13706230|RGD:13781921|RGD:15040342|RGD:15040349|RGD:152977881|RGD:153346572|RGD:155266091|RGD:155268007|RGD:155643784|RGD:155800976|RGD:21075095|RGD:243050572|RGD:243055715|RGD:243059000|RGD:243059001|RGD:243059003|RGD:243059004|RGD:26902671|RGD:38463410|RGD:401721331|RGD:401828530|RGD:401828533|RGD:401828551|RGD:40815109|RGD:8641992 (Homo sapiens) & RGD:11051461|RGD:11545851|RGD:126729812|RGD:127243935|RGD:13703605|RGD:13703607|RGD:13703609|RGD:13703612|RGD:13704254|RGD:13706230|RGD:13781921|RGD:15040342|RGD:15040349|RGD:152977881|RGD:153346572|RGD:155266091|RGD:155268007|RGD:155643784|RGD:155800976|RGD:21075095|RGD:243050572|RGD:243055715|RGD:243059000|RGD:243059001|RGD:243059003|RGD:243059004|RGD:26902671|RGD:38463410|RGD:401721331|RGD:401828530|RGD:401828533|RGD:401828551|RGD:40815109|RGD:8641992 (Homo sapiens) & RGD:11051461|RGD:11545851|RGD:126729812|RGD:127243935|RGD:13703605|RGD:13703607|RGD:13703609|RGD:13703612|RGD:13704254|RGD:13706230|RGD:13781921|RGD:15040342|RGD:15040349|RGD:152977881|RGD:153346572|RGD:155266091|RGD:155268007|RGD:155643784|RGD:155800976|RGD:21075095|RGD:243050572|RGD:243055715|RGD:243059000|RGD:243059001|RGD:243059003|RGD:243059004|RGD:26902671|RGD:38463410|RGD:401721331|RGD:401828530|RGD:401828533|RGD:401828551|RGD:40815109|RGD:8641992 (Homo sapiens) & RGD:11051461|RGD:11545851|RGD:126729812|RGD:127243935|RGD:13703605|RGD:13703607|RGD:13703609|RGD:13703612|RGD:13704254|RGD:13706230|RGD:13781921|RGD:15040342|RGD:15040349|RGD:152977881|RGD:153346572|RGD:155266091|RGD:155268007|RGD:155643784|RGD:155800976|RGD:21075095|RGD:243050572|RGD:243055715|RGD:243059000|RGD:243059001|RGD:243059003|RGD:243059004|RGD:26902671|RGD:38463410|RGD:401721331|RGD:401828530|RGD:401828533|RGD:401828551|RGD:40815109|RGD:8641992 (Homo sapiens) & RGD:11051461|RGD:11545851|RGD:126729812|RGD:127243935|RGD:13703605|RGD:13703607|RGD:13703609|RGD:13703612|RGD:13704254|RGD:13706230|RGD:13781921|RGD:15040342|RGD:15040349|RGD:152977881|RGD:153346572|RGD:155266091|RGD:155268007|RGD:155643784|RGD:155800976|RGD:21075095|RGD:243050572|RGD:243055715|RGD:243059000|RGD:243059001|RGD:243059003|RGD:243059004|RGD:26902671|RGD:38463410|RGD:401721331|RGD:401828530|RGD:401828533|RGD:401828551|RGD:40815109|RGD:8641992 (Homo sapiens) & RGD:11051461|RGD:11545851|RGD:126729812|RGD:127243935|RGD:13703605|RGD:13703607|RGD:13703609|RGD:13703612|RGD:13704254|RGD:13706230|RGD:13781921|RGD:15040342|RGD:15040349|RGD:152977881|RGD:153346572|RGD:155266091|RGD:155268007|RGD:155643784|RGD:155800976|RGD:21075095|RGD:243050572|RGD:243055715|RGD:243059000|RGD:243059001|RGD:243059003|RGD:243059004|RGD:26902671|RGD:38463410|RGD:401721331|RGD:401828530|RGD:401828533|RGD:401828551|RGD:40815109|RGD:8641992 (Homo sapiens) & RGD:11051461|RGD:11545851|RGD:126729812|RGD:127243935|RGD:13703605|RGD:13703607|RGD:13703609|RGD:13703612|RGD:13704254|RGD:13706230|RGD:13781921|RGD:15040342|RGD:15040349|RGD:152977881|RGD:153346572|RGD:155266091|RGD:155268007|RGD:155643784|RGD:155800976|RGD:21075095|RGD:243050572|RGD:243055715|RGD:243059000|RGD:243059001|RGD:243059003|RGD:243059004|RGD:26902671|RGD:38463410|RGD:401721331|RGD:401828530|RGD:401828533|RGD:401828551|RGD:40815109|RGD:8641992 (Homo sapiens) & RGD:11051461|RGD:11545851|RGD:126729812|RGD:127243935|RGD:13703605|RGD:13703607|RGD:13703609|RGD:13703612|RGD:13704254|RGD:13706230|RGD:13781921|RGD:15040342|RGD:15040349|RGD:152977881|RGD:153346572|RGD:155266091|RGD:155268007|RGD:155643784|RGD:155800976|RGD:21075095|RGD:243050572|RGD:243055715|RGD:243059000|RGD:243059001|RGD:243059003|RGD:243059004|RGD:26902671|RGD:38463410|RGD:401721331|RGD:401828530|RGD:401828533|RGD:401828551|RGD:40815109|RGD:8641992 (Homo sapiens) & RGD:11051461|RGD:11545851|RGD:126729812|RGD:127243935|RGD:13703605|RGD:13703607|RGD:13703609|RGD:13703612|RGD:13704254|RGD:13706230|RGD:13781921|RGD:15040342|RGD:15040349|RGD:152977881|RGD:153346572|RGD:155266091|RGD:155268007|RGD:155643784|RGD:155800976|RGD:21075095|RGD:243050572|RGD:243055715|RGD:243059000|RGD:243059001|RGD:243059003|RGD:243059004|RGD:26902671|RGD:38463410|RGD:401721331|RGD:401828530|RGD:401828533|RGD:401828551|RGD:40815109|RGD:8641992 (Homo sapiens)
  • 2 RGD objects have been annotated to Aarskog syndrome  (DOID:0111824)
  • 11 papers in RGD have been used to annotate FGD1
  • Curation Notes: ClinVar Annotator: match by term: Aarskog syndrome
  • Original References(s): PMID:25741868


    • An association has been curated linking FGD1 and Aarskog syndrome 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:126909408|RGD:126909409|RGD:21073725|RGD:21073726|RGD:21073729|RGD:21073730 (Homo sapiens) & RGD:126909408|RGD:126909409|RGD:21073725|RGD:21073726|RGD:21073729|RGD:21073730 (Homo sapiens) & RGD:126909408|RGD:126909409|RGD:21073725|RGD:21073726|RGD:21073729|RGD:21073730 (Homo sapiens) & RGD:126909408|RGD:126909409|RGD:21073725|RGD:21073726|RGD:21073729|RGD:21073730 (Homo sapiens) & RGD:126909408|RGD:126909409|RGD:21073725|RGD:21073726|RGD:21073729|RGD:21073730 (Homo sapiens) & RGD:126909408|RGD:126909409|RGD:21073725|RGD:21073726|RGD:21073729|RGD:21073730 (Homo sapiens)
  • 2 RGD objects have been annotated to Aarskog syndrome  (DOID:0111824)
  • 11 papers in RGD have been used to annotate FGD1
  • Curation Notes: ClinVar Annotator: match by term: Aarskog syndrome


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