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GENE - TERM ANNOTATION REPORT

3 Annotations Found.

An association has been curated linking Il1rapl1 and non-syndromic X-linked intellectual disability in Mus musculus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • 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 from sequence orthology with IL1RAPL1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 24 CRRD objects have been annotated to non-syndromic X-linked intellectual disability  (DOID:0050776)
  • 4 papers in CRRD have been used to annotate Il1rapl1
  • Curation Notes: ClinVar Annotator: match by term: Mental retardation, nonsyndromic, X-linked

  • This annotation was curated on 2019-10-15 09:02:39.0 by CRRD . For more information contact us

    An association has been curated linking Il1rapl1 and non-syndromic X-linked intellectual disability in Mus musculus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • 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 from sequence orthology with IL1RAPL1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 24 CRRD objects have been annotated to non-syndromic X-linked intellectual disability  (DOID:0050776)
  • 4 papers in CRRD have been used to annotate Il1rapl1
  • Curation Notes: ClinVar Annotator: match by term: Mental retardation, nonsyndromic, X-linked
  • Original References(s): PMID:25741868

  • This annotation was curated on 2019-10-15 09:01:38.0 by CRRD . For more information contact us

    An association has been curated linking Il1rapl1 and non-syndromic X-linked intellectual disability in Mus musculus.        

  • The association was inferred from sequence or structural similarity (ISS)
  •  
  • The annotation was made from RGD automated import pipeline for MGI gene-to-disease annotations
  • The annotation has been inferred from sequence or structural similarity with IL1RAPL1 (Homo sapiens) [(IEA) inferred from electronic annotation]
  • 24 CRRD objects have been annotated to non-syndromic X-linked intellectual disability  (DOID:0050776)
  • 4 papers in CRRD have been used to annotate Il1rapl1
  • Curation Notes: OMIM:300046 | OMIM:300047 | OMIM:300062 | OMIM:300114 | OMIM:300115 | OMIM:300143 | OMIM:300210 | OMIM:300271 | OMIM:300324 | OMIM:300355 | OMIM:300372 | OMIM:300387 | OMIM:300428 | OMIM:300433 | OMIM:300436 | OMIM:300454 | OMIM:300498 | OMIM:300504 | OMIM:300505 | OMIM:300518 | OMIM:300558 | OMIM:300577 | OMIM:300659 | OMIM:300716 | OMIM:300802 | OMIM:300803 | OMIM:300844 | OMIM:300848 | OMIM:300849 | OMIM:300850 | OMIM:300851 | OMIM:300852 | OMIM:300912 | OMIM:300919 | OMIM:300923 | OMIM:309530 | OMIM:309549

  • This annotation was curated on 2019-10-17 22:11:35.0 by CRRD . For more information contact us

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    RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.