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GENE - TERM ANNOTATION REPORT

17 Annotations Found.

An association has been curated linking APOA1-AS and primary hypoalphalipoproteinemia 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:15190838|RGD:152123261 (Homo sapiens) & RGD:15190838|RGD:152123261 (Homo sapiens)
  • 5 RGD objects have been annotated to primary hypoalphalipoproteinemia 2  (DOID:0080958)
  • 1 papers in RGD have been used to annotate APOA1-AS
  • Curation Notes: ClinVar Annotator: match by term: APOA1-related condition
  • Original References(s): PMID:28492532


    • An association has been curated linking APOA1-AS and primary hypoalphalipoproteinemia 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:8566446 (Homo sapiens)
  • 5 RGD objects have been annotated to primary hypoalphalipoproteinemia 2  (DOID:0080958)
  • 1 papers in RGD have been used to annotate APOA1-AS
  • Curation Notes: ClinVar Annotator: match by term: Hypoalphalipoproteinemia, primary, 2
  • Original References(s): PMID:25341944 PMID:25741868 PMID:28492532 PMID:7583566 PMID:7981179 PMID:8282791


    • An association has been curated linking APOA1-AS and primary hypoalphalipoproteinemia 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:8566444 (Homo sapiens)
  • 5 RGD objects have been annotated to primary hypoalphalipoproteinemia 2  (DOID:0080958)
  • 1 papers in RGD have been used to annotate APOA1-AS
  • Curation Notes: ClinVar Annotator: match by term: Hypoalphalipoproteinemia, primary, 2
  • Original References(s): PMID:1901417


    • An association has been curated linking APOA1-AS and primary hypoalphalipoproteinemia 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:8566448 (Homo sapiens)
  • 5 RGD objects have been annotated to primary hypoalphalipoproteinemia 2  (DOID:0080958)
  • 1 papers in RGD have been used to annotate APOA1-AS
  • Curation Notes: ClinVar Annotator: match by term: Hypoalphalipoproteinemia, primary, 2
  • Original References(s): PMID:7981179


    • An association has been curated linking APOA1-AS and primary hypoalphalipoproteinemia 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:8566452 (Homo sapiens)
  • 5 RGD objects have been annotated to primary hypoalphalipoproteinemia 2  (DOID:0080958)
  • 1 papers in RGD have been used to annotate APOA1-AS
  • Curation Notes: ClinVar Annotator: match by term: Hypoalphalipoproteinemia, primary, 2
  • Original References(s): PMID:9931341


    • An association has been curated linking APOA1-AS and primary hypoalphalipoproteinemia 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:405854048 (Homo sapiens)
  • 5 RGD objects have been annotated to primary hypoalphalipoproteinemia 2  (DOID:0080958)
  • 1 papers in RGD have been used to annotate APOA1-AS
  • Curation Notes: ClinVar Annotator: match by term: Hypoalphalipoproteinemia, primary, 2, intermediate
  • Original References(s): PMID:16023124


    • An association has been curated linking APOA1-AS and primary hypoalphalipoproteinemia 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:8566439 (Homo sapiens)
  • 5 RGD objects have been annotated to primary hypoalphalipoproteinemia 2  (DOID:0080958)
  • 1 papers in RGD have been used to annotate APOA1-AS
  • Curation Notes: ClinVar Annotator: match by term: HYPOALPHALIPOPROTEINEMIA, PRIMARY, 2, AUTOSOMAL DOMINANT
  • Original References(s): PMID:17665932 PMID:2123470 PMID:21296086 PMID:22952757 PMID:23233678 PMID:25741868 PMID:27464946 PMID:28492532 PMID:3142462 PMID:33502644 PMID:4304452


    • An association has been curated linking APOA1-AS and primary hypoalphalipoproteinemia 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:8566441 (Homo sapiens)
  • 5 RGD objects have been annotated to primary hypoalphalipoproteinemia 2  (DOID:0080958)
  • 1 papers in RGD have been used to annotate APOA1-AS
  • Curation Notes: ClinVar Annotator: match by term: Apolipoprotein A-I deficiency
  • Original References(s): PMID:2506176 PMID:6800349


    • An association has been curated linking APOA1-AS and primary hypoalphalipoproteinemia 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:11620323 (Homo sapiens)
  • 5 RGD objects have been annotated to primary hypoalphalipoproteinemia 2  (DOID:0080958)
  • 1 papers in RGD have been used to annotate APOA1-AS
  • Curation Notes: ClinVar Annotator: match by term: Hypoalphalipoproteinemia, primary, 2, intermediate
  • Original References(s): PMID:1901417 PMID:25741868 PMID:26530418 PMID:28492532 PMID:29083407 PMID:29353225


    • An association has been curated linking APOA1-AS and primary hypoalphalipoproteinemia 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:8566442 (Homo sapiens)
  • 5 RGD objects have been annotated to primary hypoalphalipoproteinemia 2  (DOID:0080958)
  • 1 papers in RGD have been used to annotate APOA1-AS
  • Curation Notes: ClinVar Annotator: match by term: HYPOALPHALIPOPROTEINEMIA, PRIMARY, 2, AUTOSOMAL DOMINANT
  • Original References(s): PMID:2108924 PMID:25741868 PMID:28492532


    • An association has been curated linking APOA1-AS and primary hypoalphalipoproteinemia 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:13520899 (Homo sapiens)
  • 5 RGD objects have been annotated to primary hypoalphalipoproteinemia 2  (DOID:0080958)
  • 1 papers in RGD have been used to annotate APOA1-AS
  • Curation Notes: ClinVar Annotator: match by term: Hypoalphalipoproteinemia, primary, 2, intermediate
  • Original References(s): PMID:25741868 PMID:28492532 PMID:28870971 PMID:8240372


    • An association has been curated linking APOA1-AS and primary hypoalphalipoproteinemia 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:11604996|RGD:11606053|RGD:11613478|RGD:151356442|RGD:151741971|RGD:151858106|RGD:151867392|RGD:15197706|RGD:152045089|RGD:152077176|RGD:152095459|RGD:156058003|RGD:156107812|RGD:34896232|RGD:405688506|RGD:8569225 (Homo sapiens) & RGD:11604996|RGD:11606053|RGD:11613478|RGD:151356442|RGD:151741971|RGD:151858106|RGD:151867392|RGD:15197706|RGD:152045089|RGD:152077176|RGD:152095459|RGD:156058003|RGD:156107812|RGD:34896232|RGD:405688506|RGD:8569225 (Homo sapiens) & RGD:11604996|RGD:11606053|RGD:11613478|RGD:151356442|RGD:151741971|RGD:151858106|RGD:151867392|RGD:15197706|RGD:152045089|RGD:152077176|RGD:152095459|RGD:156058003|RGD:156107812|RGD:34896232|RGD:405688506|RGD:8569225 (Homo sapiens) & RGD:11604996|RGD:11606053|RGD:11613478|RGD:151356442|RGD:151741971|RGD:151858106|RGD:151867392|RGD:15197706|RGD:152045089|RGD:152077176|RGD:152095459|RGD:156058003|RGD:156107812|RGD:34896232|RGD:405688506|RGD:8569225 (Homo sapiens) & RGD:11604996|RGD:11606053|RGD:11613478|RGD:151356442|RGD:151741971|RGD:151858106|RGD:151867392|RGD:15197706|RGD:152045089|RGD:152077176|RGD:152095459|RGD:156058003|RGD:156107812|RGD:34896232|RGD:405688506|RGD:8569225 (Homo sapiens) & RGD:11604996|RGD:11606053|RGD:11613478|RGD:151356442|RGD:151741971|RGD:151858106|RGD:151867392|RGD:15197706|RGD:152045089|RGD:152077176|RGD:152095459|RGD:156058003|RGD:156107812|RGD:34896232|RGD:405688506|RGD:8569225 (Homo sapiens) & RGD:11604996|RGD:11606053|RGD:11613478|RGD:151356442|RGD:151741971|RGD:151858106|RGD:151867392|RGD:15197706|RGD:152045089|RGD:152077176|RGD:152095459|RGD:156058003|RGD:156107812|RGD:34896232|RGD:405688506|RGD:8569225 (Homo sapiens) & RGD:11604996|RGD:11606053|RGD:11613478|RGD:151356442|RGD:151741971|RGD:151858106|RGD:151867392|RGD:15197706|RGD:152045089|RGD:152077176|RGD:152095459|RGD:156058003|RGD:156107812|RGD:34896232|RGD:405688506|RGD:8569225 (Homo sapiens) & RGD:11604996|RGD:11606053|RGD:11613478|RGD:151356442|RGD:151741971|RGD:151858106|RGD:151867392|RGD:15197706|RGD:152045089|RGD:152077176|RGD:152095459|RGD:156058003|RGD:156107812|RGD:34896232|RGD:405688506|RGD:8569225 (Homo sapiens) & RGD:11604996|RGD:11606053|RGD:11613478|RGD:151356442|RGD:151741971|RGD:151858106|RGD:151867392|RGD:15197706|RGD:152045089|RGD:152077176|RGD:152095459|RGD:156058003|RGD:156107812|RGD:34896232|RGD:405688506|RGD:8569225 (Homo sapiens) & RGD:11604996|RGD:11606053|RGD:11613478|RGD:151356442|RGD:151741971|RGD:151858106|RGD:151867392|RGD:15197706|RGD:152045089|RGD:152077176|RGD:152095459|RGD:156058003|RGD:156107812|RGD:34896232|RGD:405688506|RGD:8569225 (Homo sapiens) & RGD:11604996|RGD:11606053|RGD:11613478|RGD:151356442|RGD:151741971|RGD:151858106|RGD:151867392|RGD:15197706|RGD:152045089|RGD:152077176|RGD:152095459|RGD:156058003|RGD:156107812|RGD:34896232|RGD:405688506|RGD:8569225 (Homo sapiens) & RGD:11604996|RGD:11606053|RGD:11613478|RGD:151356442|RGD:151741971|RGD:151858106|RGD:151867392|RGD:15197706|RGD:152045089|RGD:152077176|RGD:152095459|RGD:156058003|RGD:156107812|RGD:34896232|RGD:405688506|RGD:8569225 (Homo sapiens) & RGD:11604996|RGD:11606053|RGD:11613478|RGD:151356442|RGD:151741971|RGD:151858106|RGD:151867392|RGD:15197706|RGD:152045089|RGD:152077176|RGD:152095459|RGD:156058003|RGD:156107812|RGD:34896232|RGD:405688506|RGD:8569225 (Homo sapiens) & RGD:11604996|RGD:11606053|RGD:11613478|RGD:151356442|RGD:151741971|RGD:151858106|RGD:151867392|RGD:15197706|RGD:152045089|RGD:152077176|RGD:152095459|RGD:156058003|RGD:156107812|RGD:34896232|RGD:405688506|RGD:8569225 (Homo sapiens) & RGD:11604996|RGD:11606053|RGD:11613478|RGD:151356442|RGD:151741971|RGD:151858106|RGD:151867392|RGD:15197706|RGD:152045089|RGD:152077176|RGD:152095459|RGD:156058003|RGD:156107812|RGD:34896232|RGD:405688506|RGD:8569225 (Homo sapiens)
  • 5 RGD objects have been annotated to primary hypoalphalipoproteinemia 2  (DOID:0080958)
  • 1 papers in RGD have been used to annotate APOA1-AS
  • Curation Notes: ClinVar Annotator: match by term: APOA1-related condition | ClinVar Annotator: match by term: HYPOALPHALIPOPROTEINEMIA, PRIMARY, 2, AUTOSOMAL DOMINANT | ClinVar Annotator: match by term: Hypoalphalipoproteinemia, primary, 2, intermediate
  • Original References(s): PMID:25741868 PMID:28492532


    • An association has been curated linking APOA1-AS and primary hypoalphalipoproteinemia 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:150462372|RGD:150504162|RGD:152999203|RGD:401781864|RGD:405854554|RGD:597674181|RGD:597674192|RGD:597674207|RGD:597674219|RGD:597674228|RGD:597674237|RGD:597674247|RGD:597674259|RGD:597674275|RGD:597722077 (Homo sapiens) & RGD:150462372|RGD:150504162|RGD:152999203|RGD:401781864|RGD:405854554|RGD:597674181|RGD:597674192|RGD:597674207|RGD:597674219|RGD:597674228|RGD:597674237|RGD:597674247|RGD:597674259|RGD:597674275|RGD:597722077 (Homo sapiens) & RGD:150462372|RGD:150504162|RGD:152999203|RGD:401781864|RGD:405854554|RGD:597674181|RGD:597674192|RGD:597674207|RGD:597674219|RGD:597674228|RGD:597674237|RGD:597674247|RGD:597674259|RGD:597674275|RGD:597722077 (Homo sapiens) & RGD:150462372|RGD:150504162|RGD:152999203|RGD:401781864|RGD:405854554|RGD:597674181|RGD:597674192|RGD:597674207|RGD:597674219|RGD:597674228|RGD:597674237|RGD:597674247|RGD:597674259|RGD:597674275|RGD:597722077 (Homo sapiens) & RGD:150462372|RGD:150504162|RGD:152999203|RGD:401781864|RGD:405854554|RGD:597674181|RGD:597674192|RGD:597674207|RGD:597674219|RGD:597674228|RGD:597674237|RGD:597674247|RGD:597674259|RGD:597674275|RGD:597722077 (Homo sapiens) & RGD:150462372|RGD:150504162|RGD:152999203|RGD:401781864|RGD:405854554|RGD:597674181|RGD:597674192|RGD:597674207|RGD:597674219|RGD:597674228|RGD:597674237|RGD:597674247|RGD:597674259|RGD:597674275|RGD:597722077 (Homo sapiens) & RGD:150462372|RGD:150504162|RGD:152999203|RGD:401781864|RGD:405854554|RGD:597674181|RGD:597674192|RGD:597674207|RGD:597674219|RGD:597674228|RGD:597674237|RGD:597674247|RGD:597674259|RGD:597674275|RGD:597722077 (Homo sapiens) & RGD:150462372|RGD:150504162|RGD:152999203|RGD:401781864|RGD:405854554|RGD:597674181|RGD:597674192|RGD:597674207|RGD:597674219|RGD:597674228|RGD:597674237|RGD:597674247|RGD:597674259|RGD:597674275|RGD:597722077 (Homo sapiens) & RGD:150462372|RGD:150504162|RGD:152999203|RGD:401781864|RGD:405854554|RGD:597674181|RGD:597674192|RGD:597674207|RGD:597674219|RGD:597674228|RGD:597674237|RGD:597674247|RGD:597674259|RGD:597674275|RGD:597722077 (Homo sapiens) & RGD:150462372|RGD:150504162|RGD:152999203|RGD:401781864|RGD:405854554|RGD:597674181|RGD:597674192|RGD:597674207|RGD:597674219|RGD:597674228|RGD:597674237|RGD:597674247|RGD:597674259|RGD:597674275|RGD:597722077 (Homo sapiens) & RGD:150462372|RGD:150504162|RGD:152999203|RGD:401781864|RGD:405854554|RGD:597674181|RGD:597674192|RGD:597674207|RGD:597674219|RGD:597674228|RGD:597674237|RGD:597674247|RGD:597674259|RGD:597674275|RGD:597722077 (Homo sapiens) & RGD:150462372|RGD:150504162|RGD:152999203|RGD:401781864|RGD:405854554|RGD:597674181|RGD:597674192|RGD:597674207|RGD:597674219|RGD:597674228|RGD:597674237|RGD:597674247|RGD:597674259|RGD:597674275|RGD:597722077 (Homo sapiens) & RGD:150462372|RGD:150504162|RGD:152999203|RGD:401781864|RGD:405854554|RGD:597674181|RGD:597674192|RGD:597674207|RGD:597674219|RGD:597674228|RGD:597674237|RGD:597674247|RGD:597674259|RGD:597674275|RGD:597722077 (Homo sapiens) & RGD:150462372|RGD:150504162|RGD:152999203|RGD:401781864|RGD:405854554|RGD:597674181|RGD:597674192|RGD:597674207|RGD:597674219|RGD:597674228|RGD:597674237|RGD:597674247|RGD:597674259|RGD:597674275|RGD:597722077 (Homo sapiens) & RGD:150462372|RGD:150504162|RGD:152999203|RGD:401781864|RGD:405854554|RGD:597674181|RGD:597674192|RGD:597674207|RGD:597674219|RGD:597674228|RGD:597674237|RGD:597674247|RGD:597674259|RGD:597674275|RGD:597722077 (Homo sapiens)
  • 5 RGD objects have been annotated to primary hypoalphalipoproteinemia 2  (DOID:0080958)
  • 1 papers in RGD have been used to annotate APOA1-AS
  • Curation Notes: ClinVar Annotator: match by term: HYPOALPHALIPOPROTEINEMIA, PRIMARY, 2, AUTOSOMAL DOMINANT | ClinVar Annotator: match by term: Hypoalphalipoproteinemia, primary, 2 | ClinVar Annotator: match by term: Hypoalphalipoproteinemia, primary, 2, intermediate
  • Original References(s): PMID:25741868


    • An association has been curated linking APOA1-AS and primary hypoalphalipoproteinemia 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:14689380 (Homo sapiens)
  • 5 RGD objects have been annotated to primary hypoalphalipoproteinemia 2  (DOID:0080958)
  • 1 papers in RGD have been used to annotate APOA1-AS
  • Curation Notes: ClinVar Annotator: match by term: HYPOALPHALIPOPROTEINEMIA, PRIMARY, 2, AUTOSOMAL DOMINANT
  • Original References(s): PMID:25034063 PMID:25741868 PMID:28492532


    • An association has been curated linking APOA1-AS and primary hypoalphalipoproteinemia 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:8566437 (Homo sapiens)
  • 5 RGD objects have been annotated to primary hypoalphalipoproteinemia 2  (DOID:0080958)
  • 1 papers in RGD have been used to annotate APOA1-AS
  • Curation Notes: ClinVar Annotator: match by term: HYPOALPHALIPOPROTEINEMIA, PRIMARY, 2, AUTOSOMAL DOMINANT
  • Original References(s): PMID:2512329 PMID:25741868 PMID:28492532


    • An association has been curated linking APOA1-AS and primary hypoalphalipoproteinemia 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:28906227 (Homo sapiens)
  • 5 RGD objects have been annotated to primary hypoalphalipoproteinemia 2  (DOID:0080958)
  • 1 papers in RGD have been used to annotate APOA1-AS
  • Curation Notes: ClinVar Annotator: match by term: HYPOALPHALIPOPROTEINEMIA, PRIMARY, 2, AUTOSOMAL DOMINANT
  • Original References(s): PMID:17303779 PMID:20884842 PMID:21820994 PMID:23209431 PMID:23770607 PMID:25741868 PMID:25972569 PMID:28492532 PMID:30333156 PMID:32041611 PMID:35460704


    • An association has been curated linking APOA1-AS and primary hypoalphalipoproteinemia 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:127288652 (Homo sapiens)
  • 5 RGD objects have been annotated to primary hypoalphalipoproteinemia 2  (DOID:0080958)
  • 1 papers in RGD have been used to annotate APOA1-AS
  • Curation Notes: ClinVar Annotator: match by term: HYPOALPHALIPOPROTEINEMIA, PRIMARY, 2, AUTOSOMAL DOMINANT
  • Original References(s): PMID:14986480 PMID:15131802 PMID:19324996 PMID:21296086 PMID:21458433 PMID:23806608 PMID:24603325 PMID:24650283 PMID:25741868 PMID:26193960 PMID:26515634 PMID:27540044 PMID:28492532 PMID:32861330 PMID:36988111


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