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GENE - TERM ANNOTATION REPORT

6 Annotations Found.

An association has been curated linking STON1-GTF2A1L and hypogonadism 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:11664788 (Homo sapiens)
  • 258 RGD objects have been annotated to hypogonadism  (DOID:1924)
  • 2 papers in RGD have been used to annotate STON1-GTF2A1L
  • Curation Notes: ClinVar Annotator: match by term: Hypergonadotropic hypogonadism
  • Original References(s): PMID:12679452 PMID:2244890 PMID:26467025 PMID:28492532 PMID:7556872 PMID:9851790


    • An association has been curated linking STON1-GTF2A1L and hypogonadism 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:11582988|RGD:11584493|RGD:11585480|RGD:11587217|RGD:11588947|RGD:8602917|RGD:8691852 (Homo sapiens) & RGD:11582988|RGD:11584493|RGD:11585480|RGD:11587217|RGD:11588947|RGD:8602917|RGD:8691852 (Homo sapiens) & RGD:11582988|RGD:11584493|RGD:11585480|RGD:11587217|RGD:11588947|RGD:8602917|RGD:8691852 (Homo sapiens) & RGD:11582988|RGD:11584493|RGD:11585480|RGD:11587217|RGD:11588947|RGD:8602917|RGD:8691852 (Homo sapiens) & RGD:11582988|RGD:11584493|RGD:11585480|RGD:11587217|RGD:11588947|RGD:8602917|RGD:8691852 (Homo sapiens) & RGD:11582988|RGD:11584493|RGD:11585480|RGD:11587217|RGD:11588947|RGD:8602917|RGD:8691852 (Homo sapiens) & RGD:11582988|RGD:11584493|RGD:11585480|RGD:11587217|RGD:11588947|RGD:8602917|RGD:8691852 (Homo sapiens)
  • 258 RGD objects have been annotated to hypogonadism  (DOID:1924)
  • 2 papers in RGD have been used to annotate STON1-GTF2A1L
  • Curation Notes: ClinVar Annotator: match by term: Hypergonadotropic hypogonadism
  • Original References(s): PMID:28492532


    • An association has been curated linking STON1-GTF2A1L and hypogonadism 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:11583229|RGD:11583614|RGD:11583795|RGD:11584548|RGD:11584981|RGD:11585434|RGD:11585614|RGD:11586166|RGD:11586667|RGD:11587510|RGD:11587541|RGD:11587791|RGD:11589412|RGD:11589532|RGD:11589711|RGD:11589976|RGD:11646703|RGD:11647689|RGD:11653177 (Homo sapiens) & RGD:11583229|RGD:11583614|RGD:11583795|RGD:11584548|RGD:11584981|RGD:11585434|RGD:11585614|RGD:11586166|RGD:11586667|RGD:11587510|RGD:11587541|RGD:11587791|RGD:11589412|RGD:11589532|RGD:11589711|RGD:11589976|RGD:11646703|RGD:11647689|RGD:11653177 (Homo sapiens) & RGD:11583229|RGD:11583614|RGD:11583795|RGD:11584548|RGD:11584981|RGD:11585434|RGD:11585614|RGD:11586166|RGD:11586667|RGD:11587510|RGD:11587541|RGD:11587791|RGD:11589412|RGD:11589532|RGD:11589711|RGD:11589976|RGD:11646703|RGD:11647689|RGD:11653177 (Homo sapiens) & RGD:11583229|RGD:11583614|RGD:11583795|RGD:11584548|RGD:11584981|RGD:11585434|RGD:11585614|RGD:11586166|RGD:11586667|RGD:11587510|RGD:11587541|RGD:11587791|RGD:11589412|RGD:11589532|RGD:11589711|RGD:11589976|RGD:11646703|RGD:11647689|RGD:11653177 (Homo sapiens) & RGD:11583229|RGD:11583614|RGD:11583795|RGD:11584548|RGD:11584981|RGD:11585434|RGD:11585614|RGD:11586166|RGD:11586667|RGD:11587510|RGD:11587541|RGD:11587791|RGD:11589412|RGD:11589532|RGD:11589711|RGD:11589976|RGD:11646703|RGD:11647689|RGD:11653177 (Homo sapiens) & RGD:11583229|RGD:11583614|RGD:11583795|RGD:11584548|RGD:11584981|RGD:11585434|RGD:11585614|RGD:11586166|RGD:11586667|RGD:11587510|RGD:11587541|RGD:11587791|RGD:11589412|RGD:11589532|RGD:11589711|RGD:11589976|RGD:11646703|RGD:11647689|RGD:11653177 (Homo sapiens) & RGD:11583229|RGD:11583614|RGD:11583795|RGD:11584548|RGD:11584981|RGD:11585434|RGD:11585614|RGD:11586166|RGD:11586667|RGD:11587510|RGD:11587541|RGD:11587791|RGD:11589412|RGD:11589532|RGD:11589711|RGD:11589976|RGD:11646703|RGD:11647689|RGD:11653177 (Homo sapiens) & RGD:11583229|RGD:11583614|RGD:11583795|RGD:11584548|RGD:11584981|RGD:11585434|RGD:11585614|RGD:11586166|RGD:11586667|RGD:11587510|RGD:11587541|RGD:11587791|RGD:11589412|RGD:11589532|RGD:11589711|RGD:11589976|RGD:11646703|RGD:11647689|RGD:11653177 (Homo sapiens) & RGD:11583229|RGD:11583614|RGD:11583795|RGD:11584548|RGD:11584981|RGD:11585434|RGD:11585614|RGD:11586166|RGD:11586667|RGD:11587510|RGD:11587541|RGD:11587791|RGD:11589412|RGD:11589532|RGD:11589711|RGD:11589976|RGD:11646703|RGD:11647689|RGD:11653177 (Homo sapiens) & RGD:11583229|RGD:11583614|RGD:11583795|RGD:11584548|RGD:11584981|RGD:11585434|RGD:11585614|RGD:11586166|RGD:11586667|RGD:11587510|RGD:11587541|RGD:11587791|RGD:11589412|RGD:11589532|RGD:11589711|RGD:11589976|RGD:11646703|RGD:11647689|RGD:11653177 (Homo sapiens) & RGD:11583229|RGD:11583614|RGD:11583795|RGD:11584548|RGD:11584981|RGD:11585434|RGD:11585614|RGD:11586166|RGD:11586667|RGD:11587510|RGD:11587541|RGD:11587791|RGD:11589412|RGD:11589532|RGD:11589711|RGD:11589976|RGD:11646703|RGD:11647689|RGD:11653177 (Homo sapiens) & RGD:11583229|RGD:11583614|RGD:11583795|RGD:11584548|RGD:11584981|RGD:11585434|RGD:11585614|RGD:11586166|RGD:11586667|RGD:11587510|RGD:11587541|RGD:11587791|RGD:11589412|RGD:11589532|RGD:11589711|RGD:11589976|RGD:11646703|RGD:11647689|RGD:11653177 (Homo sapiens) & RGD:11583229|RGD:11583614|RGD:11583795|RGD:11584548|RGD:11584981|RGD:11585434|RGD:11585614|RGD:11586166|RGD:11586667|RGD:11587510|RGD:11587541|RGD:11587791|RGD:11589412|RGD:11589532|RGD:11589711|RGD:11589976|RGD:11646703|RGD:11647689|RGD:11653177 (Homo sapiens) & RGD:11583229|RGD:11583614|RGD:11583795|RGD:11584548|RGD:11584981|RGD:11585434|RGD:11585614|RGD:11586166|RGD:11586667|RGD:11587510|RGD:11587541|RGD:11587791|RGD:11589412|RGD:11589532|RGD:11589711|RGD:11589976|RGD:11646703|RGD:11647689|RGD:11653177 (Homo sapiens) & RGD:11583229|RGD:11583614|RGD:11583795|RGD:11584548|RGD:11584981|RGD:11585434|RGD:11585614|RGD:11586166|RGD:11586667|RGD:11587510|RGD:11587541|RGD:11587791|RGD:11589412|RGD:11589532|RGD:11589711|RGD:11589976|RGD:11646703|RGD:11647689|RGD:11653177 (Homo sapiens) & RGD:11583229|RGD:11583614|RGD:11583795|RGD:11584548|RGD:11584981|RGD:11585434|RGD:11585614|RGD:11586166|RGD:11586667|RGD:11587510|RGD:11587541|RGD:11587791|RGD:11589412|RGD:11589532|RGD:11589711|RGD:11589976|RGD:11646703|RGD:11647689|RGD:11653177 (Homo sapiens) & RGD:11583229|RGD:11583614|RGD:11583795|RGD:11584548|RGD:11584981|RGD:11585434|RGD:11585614|RGD:11586166|RGD:11586667|RGD:11587510|RGD:11587541|RGD:11587791|RGD:11589412|RGD:11589532|RGD:11589711|RGD:11589976|RGD:11646703|RGD:11647689|RGD:11653177 (Homo sapiens) & RGD:11583229|RGD:11583614|RGD:11583795|RGD:11584548|RGD:11584981|RGD:11585434|RGD:11585614|RGD:11586166|RGD:11586667|RGD:11587510|RGD:11587541|RGD:11587791|RGD:11589412|RGD:11589532|RGD:11589711|RGD:11589976|RGD:11646703|RGD:11647689|RGD:11653177 (Homo sapiens) & RGD:11583229|RGD:11583614|RGD:11583795|RGD:11584548|RGD:11584981|RGD:11585434|RGD:11585614|RGD:11586166|RGD:11586667|RGD:11587510|RGD:11587541|RGD:11587791|RGD:11589412|RGD:11589532|RGD:11589711|RGD:11589976|RGD:11646703|RGD:11647689|RGD:11653177 (Homo sapiens)
  • 258 RGD objects have been annotated to hypogonadism  (DOID:1924)
  • 2 papers in RGD have been used to annotate STON1-GTF2A1L
  • Curation Notes: ClinVar Annotator: match by term: Hypergonadotropic hypogonadism


    • An association has been curated linking STON1-GTF2A1L and hypogonadism 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:11583518|RGD:11585294 (Homo sapiens) & RGD:11583518|RGD:11585294 (Homo sapiens)
  • 258 RGD objects have been annotated to hypogonadism  (DOID:1924)
  • 2 papers in RGD have been used to annotate STON1-GTF2A1L
  • Curation Notes: ClinVar Annotator: match by term: Hypergonadotropic hypogonadism
  • Original References(s): PMID:25741868


    • An association has been curated linking STON1-GTF2A1L and hypogonadism 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:11584132|RGD:11586408 (Homo sapiens) & RGD:11584132|RGD:11586408 (Homo sapiens)
  • 258 RGD objects have been annotated to hypogonadism  (DOID:1924)
  • 2 papers in RGD have been used to annotate STON1-GTF2A1L
  • Curation Notes: ClinVar Annotator: match by term: Hypergonadotropic hypogonadism
  • Original References(s): PMID:25741868 PMID:28492532


    • An association has been curated linking STON1-GTF2A1L and hypogonadism 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:11543955|RGD:11547555|RGD:11548938 (Homo sapiens) & RGD:11543955|RGD:11547555|RGD:11548938 (Homo sapiens) & RGD:11543955|RGD:11547555|RGD:11548938 (Homo sapiens)
  • 258 RGD objects have been annotated to hypogonadism  (DOID:1924)
  • 2 papers in RGD have been used to annotate STON1-GTF2A1L
  • Curation Notes: ClinVar Annotator: match by term: Hypergonadotropic hypogonadism
  • Original References(s): PMID:25741868 PMID:26467025 PMID:28492532


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