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GENE - TERM ANNOTATION REPORT

RGD ID: 1351414
Species: Homo sapiens
RGD Object: Gene
Symbol: RANBP2
Name: RAN binding protein 2
Acc ID: DOID:0111663
Term: ectodermal dysplasia 10A
Definition: A hypohidrotic ectodermal dysplasia that has_material_basis_in heterozygous mutation in the EDAR gene on chromosome 2q13. (DO)
Definition Source(s): https://www.ncbi.nlm.nih.gov/pubmed/10431241 "DO" "DO"
Note: Use of the qualifier "multiple interactions" designates that the annotated interaction is comprised of a complex set of reactions and/or regulatory events, possibly involving additional chemicals and/or gene products.
Object SymbolQualifierEvidenceWithReferenceSourceNotesOriginal Reference(s)
RANBP2 IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Ectodermal dysplasia 10A, hypohidrotic/hair/nail type, autosomal dominantPMID:16029325 PMID:22032522 PMID:28492532
RANBP2 IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Autosomal dominant hypohidrotic ectodermal dysplasiaPMID:24033266
RANBP2 IAGP (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Ectodermal dysplasia 10A, hypohidrotic/hair/nail type, autosomal dominantPMID:25741868 PMID:28492532
RANBP2 IAGP (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Ectodermal dysplasia 10A, hypohidrotic/hair/nail type, autosomal dominantPMID:28492532
RANBP2 IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Ectodermal dysplasia 10A, hypohidrotic/hair/nail type, autosomal dominantPMID:19438931 PMID:21876339 PMID:23991204 PMID:25741868 PMID:28492532
RANBP2 IAGP (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Ectodermal dysplasia 10A, hypohidrotic/hair/nail type, autosomal dominantPMID:23401279 PMID:24641098 PMID:28492532
RANBP2 IAGP (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Ectodermal dysplasia 10A, hypohidrotic/hair/nail type, autosomal dominant 
RANBP2 IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Ectodermal dysplasia 10A, hypohidrotic/hair/nail type, autosomal dominantPMID:28265457 PMID:28492532
RANBP2 IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Ectodermal dysplasia 10A, hypohidrotic/hair/nail type, autosomal dominantPMID:10431241 PMID:16199547 PMID:20979233 PMID:28492532 PMID:28981473
RANBP2 IAGP (Homo sapiens) or (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Ectodermal dysplasia 10A, hypohidrotic/hair/nail type, autosomal dominantPMID:10431241 PMID:10431242 PMID:20979233 PMID:28492532 PMID:28981473
RANBP2 IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Ectodermal dysplasia 10A, hypohidrotic/hair/nail type, autosomal dominantPMID:21771270 PMID:28492532
RANBP2 IAGP (Homo sapiens) or (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Ectodermal dysplasia 10A, hypohidrotic/hair/nail type, autosomal dominantPMID:17576681 PMID:23401279 PMID:24641098 PMID:28492532 PMID:9536098
RANBP2 IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Ectodermal dysplasia 10A, hypohidrotic/hair/nail type, autosomal dominantPMID:22032522 PMID:25741868 PMID:28492532
RANBP2 IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Ectodermal dysplasia 10A, hypohidrotic/hair/nail type, autosomal dominantPMID:18231121 PMID:20236127 PMID:20979233 PMID:28492532
RANBP2 IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Ectodermal dysplasia 10A, hypohidrotic/hair/nail type, autosomal dominantPMID:10431241 PMID:20979233 PMID:28492532
RANBP2 IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Ectodermal dysplasia 10A, hypohidrotic/hair/nail type, autosomal dominantPMID:10431241 PMID:16199547 PMID:20979233 PMID:28492532
RANBP2 IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Ectodermal dysplasia 10A, hypohidrotic/hair/nail type, autosomal dominantPMID:16435307 PMID:28492532
RANBP2 IAGP (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Ectodermal dysplasia 10A, hypohidrotic/hair/nail type, autosomal dominantPMID:25741868
RANBP2 IAGP (Homo sapiens) or (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Ectodermal dysplasia 10A, hypohidrotic/hair/nail type, autosomal dominantPMID:20236127 PMID:20979233 PMID:28492532
RANBP2 IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Ectodermal dysplasia 10A, hypohidrotic/hair/nail type, autosomal dominantPMID:10431241 PMID:10431242 PMID:20979233 PMID:28492532 PMID:28981473 PMID:32274043
RANBP2 IAGP (Homo sapiens) or (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Ectodermal dysplasia 10A, hypohidrotic/hair/nail type, autosomal dominantPMID:17576681 PMID:28492532 PMID:9536098
RANBP2 IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Ectodermal dysplasia 10A, hypohidrotic/hair/nail type, autosomal dominantPMID:28492532 PMID:32325225
RANBP2 IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Ectodermal dysplasia 10A, hypohidrotic/hair/nail type, autosomal dominantPMID:10431241 PMID:10431242 PMID:18854857 PMID:20979233 PMID:28492532 PMID:28981473
RANBP2 IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Ectodermal dysplasia 10A, hypohidrotic/hair/nail type, autosomal dominantPMID:23401279 PMID:24641098 PMID:27305980 PMID:28492532
RANBP2 IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Ectodermal dysplasia 10A, hypohidrotic/hair/nail type, autosomal dominantPMID:23991204 PMID:28492532
RANBP2 IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Ectodermal dysplasia 10A, hypohidrotic/hair/nail type, autosomal dominantPMID:10431241 PMID:17125505 PMID:27305980 PMID:28492532
RANBP2 IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Ectodermal dysplasia 10A, hypohidrotic/hair/nail type, autosomal dominantPMID:10431242 PMID:15013427 PMID:23991204 PMID:28492532
RANBP2 IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Ectodermal dysplasia 10A, hypohidrotic/hair/nail type, autosomal dominantPMID:25741868 PMID:33205897
RANBP2 IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Ectodermal dysplasia 10a, hypohidrotic/hair/tooth type, autosomal dominantPMID:10431241 PMID:18231121 PMID:20236127 PMID:20979233 PMID:25741868 PMID:28492532
RANBP2 IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Ectodermal dysplasia 10A, hypohidrotic/hair/nail type, autosomal dominantPMID:10431241 PMID:11279189 PMID:28492532
RANBP2 IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Ectodermal dysplasia 10a, hypohidrotic/hair/tooth type, autosomal dominantPMID:10431241 PMID:17125505 PMID:24884697 PMID:25741868 PMID:26336973 PMID:27305980 PMID:28492532
RANBP2 IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Ectodermal dysplasia 10a, hypohidrotic/hair/tooth type, autosomal dominantPMID:10431241 PMID:11035039 PMID:15013427 PMID:16435307 PMID:18231121 PMID:20979233 PMID:23401279 PMID:25741868 PMID:27657131 PMID:28492532
RANBP2 IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Ectodermal dysplasia 10a, hypohidrotic/hair/tooth type, autosomal dominantPMID:18231121
RANBP2 IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Ectodermal Dysplasia 3, AnhidroticPMID:18065779 PMID:18561327 PMID:18704500 PMID:25741868 PMID:28492532
RANBP2 IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Ectodermal dysplasia 10A, hypohidrotic/hair/nail type, autosomal dominantPMID:19438931 PMID:22032522 PMID:28492532
RANBP2 IAGP (Homo sapiens) or (Homo sapiens) or (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Ectodermal dysplasia 10A, hypohidrotic/hair/nail type, autosomal dominantPMID:24033266 PMID:25741868 PMID:28492532
RANBP2 IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Autosomal dominant hypohidrotic ectodermal dysplasiaPMID:10431241 PMID:18854857 PMID:24033266
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