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GENE - TERM ANNOTATION REPORT

4 Annotations Found.

An association has been curated linking PIK3R2 and genetic disease 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:8570652 (Homo sapiens)
  • 33187 RGD objects have been annotated to genetic disease  (DOID:630)
  • 13 papers in RGD have been used to annotate PIK3R2
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
  • Original References(s): PMID:16357568 PMID:21984976 PMID:22729224 PMID:24497998 PMID:25741868 PMID:26520804 PMID:26860062 PMID:27854409 PMID:28086757 PMID:28492532 PMID:28502725 PMID:33818783


    • An association has been curated linking PIK3R2 and genetic disease 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:150437137 (Homo sapiens)
  • 33187 RGD objects have been annotated to genetic disease  (DOID:630)
  • 13 papers in RGD have been used to annotate PIK3R2
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
  • Original References(s): PMID:25741868 PMID:28492532


    • An association has been curated linking PIK3R2 and genetic disease 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:151771672|RGD:151789539|RGD:151829747|RGD:15201133|RGD:152132485|RGD:156060560|RGD:156168038|RGD:156219934|RGD:156338722|RGD:156359666|RGD:26900294|RGD:38500016|RGD:401764302 (Homo sapiens) & RGD:151771672|RGD:151789539|RGD:151829747|RGD:15201133|RGD:152132485|RGD:156060560|RGD:156168038|RGD:156219934|RGD:156338722|RGD:156359666|RGD:26900294|RGD:38500016|RGD:401764302 (Homo sapiens) & RGD:151771672|RGD:151789539|RGD:151829747|RGD:15201133|RGD:152132485|RGD:156060560|RGD:156168038|RGD:156219934|RGD:156338722|RGD:156359666|RGD:26900294|RGD:38500016|RGD:401764302 (Homo sapiens) & RGD:151771672|RGD:151789539|RGD:151829747|RGD:15201133|RGD:152132485|RGD:156060560|RGD:156168038|RGD:156219934|RGD:156338722|RGD:156359666|RGD:26900294|RGD:38500016|RGD:401764302 (Homo sapiens) & RGD:151771672|RGD:151789539|RGD:151829747|RGD:15201133|RGD:152132485|RGD:156060560|RGD:156168038|RGD:156219934|RGD:156338722|RGD:156359666|RGD:26900294|RGD:38500016|RGD:401764302 (Homo sapiens) & RGD:151771672|RGD:151789539|RGD:151829747|RGD:15201133|RGD:152132485|RGD:156060560|RGD:156168038|RGD:156219934|RGD:156338722|RGD:156359666|RGD:26900294|RGD:38500016|RGD:401764302 (Homo sapiens) & RGD:151771672|RGD:151789539|RGD:151829747|RGD:15201133|RGD:152132485|RGD:156060560|RGD:156168038|RGD:156219934|RGD:156338722|RGD:156359666|RGD:26900294|RGD:38500016|RGD:401764302 (Homo sapiens) & RGD:151771672|RGD:151789539|RGD:151829747|RGD:15201133|RGD:152132485|RGD:156060560|RGD:156168038|RGD:156219934|RGD:156338722|RGD:156359666|RGD:26900294|RGD:38500016|RGD:401764302 (Homo sapiens) & RGD:151771672|RGD:151789539|RGD:151829747|RGD:15201133|RGD:152132485|RGD:156060560|RGD:156168038|RGD:156219934|RGD:156338722|RGD:156359666|RGD:26900294|RGD:38500016|RGD:401764302 (Homo sapiens) & RGD:151771672|RGD:151789539|RGD:151829747|RGD:15201133|RGD:152132485|RGD:156060560|RGD:156168038|RGD:156219934|RGD:156338722|RGD:156359666|RGD:26900294|RGD:38500016|RGD:401764302 (Homo sapiens) & RGD:151771672|RGD:151789539|RGD:151829747|RGD:15201133|RGD:152132485|RGD:156060560|RGD:156168038|RGD:156219934|RGD:156338722|RGD:156359666|RGD:26900294|RGD:38500016|RGD:401764302 (Homo sapiens) & RGD:151771672|RGD:151789539|RGD:151829747|RGD:15201133|RGD:152132485|RGD:156060560|RGD:156168038|RGD:156219934|RGD:156338722|RGD:156359666|RGD:26900294|RGD:38500016|RGD:401764302 (Homo sapiens) & RGD:151771672|RGD:151789539|RGD:151829747|RGD:15201133|RGD:152132485|RGD:156060560|RGD:156168038|RGD:156219934|RGD:156338722|RGD:156359666|RGD:26900294|RGD:38500016|RGD:401764302 (Homo sapiens)
  • 33187 RGD objects have been annotated to genetic disease  (DOID:630)
  • 13 papers in RGD have been used to annotate PIK3R2
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
  • Original References(s): PMID:28492532


    • An association has been curated linking PIK3R2 and genetic disease 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:155947948|RGD:155989924|RGD:156015442|RGD:156047955|RGD:156075373|RGD:156130499|RGD:156185917|RGD:156188429|RGD:156222212|RGD:156223068|RGD:156257288|RGD:156328789|RGD:156358240|RGD:329359492|RGD:329364482|RGD:329376815|RGD:329391705|RGD:401751998|RGD:401764970|RGD:401863787|RGD:401872492|RGD:401882818|RGD:401898202 (Homo sapiens) & RGD:155947948|RGD:155989924|RGD:156015442|RGD:156047955|RGD:156075373|RGD:156130499|RGD:156185917|RGD:156188429|RGD:156222212|RGD:156223068|RGD:156257288|RGD:156328789|RGD:156358240|RGD:329359492|RGD:329364482|RGD:329376815|RGD:329391705|RGD:401751998|RGD:401764970|RGD:401863787|RGD:401872492|RGD:401882818|RGD:401898202 (Homo sapiens) & RGD:155947948|RGD:155989924|RGD:156015442|RGD:156047955|RGD:156075373|RGD:156130499|RGD:156185917|RGD:156188429|RGD:156222212|RGD:156223068|RGD:156257288|RGD:156328789|RGD:156358240|RGD:329359492|RGD:329364482|RGD:329376815|RGD:329391705|RGD:401751998|RGD:401764970|RGD:401863787|RGD:401872492|RGD:401882818|RGD:401898202 (Homo sapiens) & RGD:155947948|RGD:155989924|RGD:156015442|RGD:156047955|RGD:156075373|RGD:156130499|RGD:156185917|RGD:156188429|RGD:156222212|RGD:156223068|RGD:156257288|RGD:156328789|RGD:156358240|RGD:329359492|RGD:329364482|RGD:329376815|RGD:329391705|RGD:401751998|RGD:401764970|RGD:401863787|RGD:401872492|RGD:401882818|RGD:401898202 (Homo sapiens) & RGD:155947948|RGD:155989924|RGD:156015442|RGD:156047955|RGD:156075373|RGD:156130499|RGD:156185917|RGD:156188429|RGD:156222212|RGD:156223068|RGD:156257288|RGD:156328789|RGD:156358240|RGD:329359492|RGD:329364482|RGD:329376815|RGD:329391705|RGD:401751998|RGD:401764970|RGD:401863787|RGD:401872492|RGD:401882818|RGD:401898202 (Homo sapiens) & RGD:155947948|RGD:155989924|RGD:156015442|RGD:156047955|RGD:156075373|RGD:156130499|RGD:156185917|RGD:156188429|RGD:156222212|RGD:156223068|RGD:156257288|RGD:156328789|RGD:156358240|RGD:329359492|RGD:329364482|RGD:329376815|RGD:329391705|RGD:401751998|RGD:401764970|RGD:401863787|RGD:401872492|RGD:401882818|RGD:401898202 (Homo sapiens) & RGD:155947948|RGD:155989924|RGD:156015442|RGD:156047955|RGD:156075373|RGD:156130499|RGD:156185917|RGD:156188429|RGD:156222212|RGD:156223068|RGD:156257288|RGD:156328789|RGD:156358240|RGD:329359492|RGD:329364482|RGD:329376815|RGD:329391705|RGD:401751998|RGD:401764970|RGD:401863787|RGD:401872492|RGD:401882818|RGD:401898202 (Homo sapiens) & RGD:155947948|RGD:155989924|RGD:156015442|RGD:156047955|RGD:156075373|RGD:156130499|RGD:156185917|RGD:156188429|RGD:156222212|RGD:156223068|RGD:156257288|RGD:156328789|RGD:156358240|RGD:329359492|RGD:329364482|RGD:329376815|RGD:329391705|RGD:401751998|RGD:401764970|RGD:401863787|RGD:401872492|RGD:401882818|RGD:401898202 (Homo sapiens) & RGD:155947948|RGD:155989924|RGD:156015442|RGD:156047955|RGD:156075373|RGD:156130499|RGD:156185917|RGD:156188429|RGD:156222212|RGD:156223068|RGD:156257288|RGD:156328789|RGD:156358240|RGD:329359492|RGD:329364482|RGD:329376815|RGD:329391705|RGD:401751998|RGD:401764970|RGD:401863787|RGD:401872492|RGD:401882818|RGD:401898202 (Homo sapiens) & RGD:155947948|RGD:155989924|RGD:156015442|RGD:156047955|RGD:156075373|RGD:156130499|RGD:156185917|RGD:156188429|RGD:156222212|RGD:156223068|RGD:156257288|RGD:156328789|RGD:156358240|RGD:329359492|RGD:329364482|RGD:329376815|RGD:329391705|RGD:401751998|RGD:401764970|RGD:401863787|RGD:401872492|RGD:401882818|RGD:401898202 (Homo sapiens) & RGD:155947948|RGD:155989924|RGD:156015442|RGD:156047955|RGD:156075373|RGD:156130499|RGD:156185917|RGD:156188429|RGD:156222212|RGD:156223068|RGD:156257288|RGD:156328789|RGD:156358240|RGD:329359492|RGD:329364482|RGD:329376815|RGD:329391705|RGD:401751998|RGD:401764970|RGD:401863787|RGD:401872492|RGD:401882818|RGD:401898202 (Homo sapiens) & RGD:155947948|RGD:155989924|RGD:156015442|RGD:156047955|RGD:156075373|RGD:156130499|RGD:156185917|RGD:156188429|RGD:156222212|RGD:156223068|RGD:156257288|RGD:156328789|RGD:156358240|RGD:329359492|RGD:329364482|RGD:329376815|RGD:329391705|RGD:401751998|RGD:401764970|RGD:401863787|RGD:401872492|RGD:401882818|RGD:401898202 (Homo sapiens) & RGD:155947948|RGD:155989924|RGD:156015442|RGD:156047955|RGD:156075373|RGD:156130499|RGD:156185917|RGD:156188429|RGD:156222212|RGD:156223068|RGD:156257288|RGD:156328789|RGD:156358240|RGD:329359492|RGD:329364482|RGD:329376815|RGD:329391705|RGD:401751998|RGD:401764970|RGD:401863787|RGD:401872492|RGD:401882818|RGD:401898202 (Homo sapiens) & RGD:155947948|RGD:155989924|RGD:156015442|RGD:156047955|RGD:156075373|RGD:156130499|RGD:156185917|RGD:156188429|RGD:156222212|RGD:156223068|RGD:156257288|RGD:156328789|RGD:156358240|RGD:329359492|RGD:329364482|RGD:329376815|RGD:329391705|RGD:401751998|RGD:401764970|RGD:401863787|RGD:401872492|RGD:401882818|RGD:401898202 (Homo sapiens) & RGD:155947948|RGD:155989924|RGD:156015442|RGD:156047955|RGD:156075373|RGD:156130499|RGD:156185917|RGD:156188429|RGD:156222212|RGD:156223068|RGD:156257288|RGD:156328789|RGD:156358240|RGD:329359492|RGD:329364482|RGD:329376815|RGD:329391705|RGD:401751998|RGD:401764970|RGD:401863787|RGD:401872492|RGD:401882818|RGD:401898202 (Homo sapiens) & RGD:155947948|RGD:155989924|RGD:156015442|RGD:156047955|RGD:156075373|RGD:156130499|RGD:156185917|RGD:156188429|RGD:156222212|RGD:156223068|RGD:156257288|RGD:156328789|RGD:156358240|RGD:329359492|RGD:329364482|RGD:329376815|RGD:329391705|RGD:401751998|RGD:401764970|RGD:401863787|RGD:401872492|RGD:401882818|RGD:401898202 (Homo sapiens) & RGD:155947948|RGD:155989924|RGD:156015442|RGD:156047955|RGD:156075373|RGD:156130499|RGD:156185917|RGD:156188429|RGD:156222212|RGD:156223068|RGD:156257288|RGD:156328789|RGD:156358240|RGD:329359492|RGD:329364482|RGD:329376815|RGD:329391705|RGD:401751998|RGD:401764970|RGD:401863787|RGD:401872492|RGD:401882818|RGD:401898202 (Homo sapiens) & RGD:155947948|RGD:155989924|RGD:156015442|RGD:156047955|RGD:156075373|RGD:156130499|RGD:156185917|RGD:156188429|RGD:156222212|RGD:156223068|RGD:156257288|RGD:156328789|RGD:156358240|RGD:329359492|RGD:329364482|RGD:329376815|RGD:329391705|RGD:401751998|RGD:401764970|RGD:401863787|RGD:401872492|RGD:401882818|RGD:401898202 (Homo sapiens) & RGD:155947948|RGD:155989924|RGD:156015442|RGD:156047955|RGD:156075373|RGD:156130499|RGD:156185917|RGD:156188429|RGD:156222212|RGD:156223068|RGD:156257288|RGD:156328789|RGD:156358240|RGD:329359492|RGD:329364482|RGD:329376815|RGD:329391705|RGD:401751998|RGD:401764970|RGD:401863787|RGD:401872492|RGD:401882818|RGD:401898202 (Homo sapiens) & RGD:155947948|RGD:155989924|RGD:156015442|RGD:156047955|RGD:156075373|RGD:156130499|RGD:156185917|RGD:156188429|RGD:156222212|RGD:156223068|RGD:156257288|RGD:156328789|RGD:156358240|RGD:329359492|RGD:329364482|RGD:329376815|RGD:329391705|RGD:401751998|RGD:401764970|RGD:401863787|RGD:401872492|RGD:401882818|RGD:401898202 (Homo sapiens) & RGD:155947948|RGD:155989924|RGD:156015442|RGD:156047955|RGD:156075373|RGD:156130499|RGD:156185917|RGD:156188429|RGD:156222212|RGD:156223068|RGD:156257288|RGD:156328789|RGD:156358240|RGD:329359492|RGD:329364482|RGD:329376815|RGD:329391705|RGD:401751998|RGD:401764970|RGD:401863787|RGD:401872492|RGD:401882818|RGD:401898202 (Homo sapiens) & RGD:155947948|RGD:155989924|RGD:156015442|RGD:156047955|RGD:156075373|RGD:156130499|RGD:156185917|RGD:156188429|RGD:156222212|RGD:156223068|RGD:156257288|RGD:156328789|RGD:156358240|RGD:329359492|RGD:329364482|RGD:329376815|RGD:329391705|RGD:401751998|RGD:401764970|RGD:401863787|RGD:401872492|RGD:401882818|RGD:401898202 (Homo sapiens) & RGD:155947948|RGD:155989924|RGD:156015442|RGD:156047955|RGD:156075373|RGD:156130499|RGD:156185917|RGD:156188429|RGD:156222212|RGD:156223068|RGD:156257288|RGD:156328789|RGD:156358240|RGD:329359492|RGD:329364482|RGD:329376815|RGD:329391705|RGD:401751998|RGD:401764970|RGD:401863787|RGD:401872492|RGD:401882818|RGD:401898202 (Homo sapiens)
  • 33187 RGD objects have been annotated to genetic disease  (DOID:630)
  • 13 papers in RGD have been used to annotate PIK3R2
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases


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