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GENE - TERM ANNOTATION REPORT

RGD ID: 38637361
Species: Homo sapiens
RGD Object: Gene
Symbol: CLDN14-AS1
Name: CLDN14 antisense RNA 1
Acc ID: DOID:0110487
Term: autosomal recessive nonsyndromic deafness 29
Definition: An autosomal recessive nonsyndromic deafness that is characterized by prelingual onset with severe to profound, stable hearing loss and has_material_basis_in mutation in the CLDN14 gene on chromosome 21q22. (DO)
Definition Source(s): PMID:11163249 "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)
CLDN14-AS1 IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: CLDN14-related conditionPMID:22246673 PMID:23235333 PMID:25741868 PMID:28492532 PMID:30311386
CLDN14-AS1 IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: CLDN14-related conditionPMID:22246673 PMID:25741868
CLDN14-AS1 IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Deafness, autosomal recessive 29PMID:22246673
CLDN14-AS1 IAGP (Homo sapiens) or (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: CLDN14-related conditionPMID:24033266
CLDN14-AS1 IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Deafness, autosomal recessive 29PMID:23991001 PMID:24033266 PMID:25741868 PMID:26969326 PMID:27838790 PMID:28492532
CLDN14-AS1 IAGP (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: Deafness, autosomal recessive 29PMID:25741868
CLDN14-AS1 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)8554872ClinVarClinVar Annotator: match by term: Deafness, autosomal recessive 29 
CLDN14-AS1 IAGP (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: CLDN14-related condition | ClinVar Annotator: match by term: Deafness, autosomal recessive 29PMID:28492532
CLDN14-AS1 IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Deafness, autosomal recessive 29PMID:25741868 PMID:28492532
CLDN14-AS1 IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Deafness, autosomal recessive 29PMID:25741868 PMID:28492532 PMID:30311386
CLDN14-AS1 IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Deafness, autosomal recessive 29PMID:23991001 PMID:28492532
CLDN14-AS1 IAGP (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Deafness, autosomal recessive 29PMID:30311386
CLDN14-AS1 IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Deafness, autosomal recessive 29PMID:11163249
CLDN14-AS1 IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Deafness, autosomal recessive 29PMID:11163249 PMID:15880785 PMID:22246673 PMID:25741868 PMID:30303587
CLDN14-AS1 IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Deafness, autosomal recessive 29PMID:15880785 PMID:25741868 PMID:28492532 PMID:33105617
CLDN14-AS1 IAGP (Homo sapiens) or (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Deafness, autosomal recessive 29PMID:24033266 PMID:25741868 PMID:26467025 PMID:28492532
CLDN14-AS1 IAGP (Homo sapiens) or (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Deafness, autosomal recessive 29PMID:24033266 PMID:25741868 PMID:28492532
CLDN14-AS1 IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: CLDN14-related conditionPMID:23590985 PMID:24033266 PMID:28492532
CLDN14-AS1 IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Deafness, autosomal recessive 29PMID:23590985 PMID:24033266 PMID:25741868 PMID:26467025 PMID:28492532
CLDN14-AS1 IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Deafness, autosomal recessive 29PMID:24033266 PMID:28492532
CLDN14-AS1 IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Deafness, autosomal recessive 29PMID:15880785 PMID:23590985 PMID:24033266 PMID:25741868 PMID:26467025 PMID:28492532
CLDN14-AS1 IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Deafness, autosomal recessive 29PMID:15880785 PMID:24033266 PMID:28492532
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