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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:9004538
Term: Hearing Loss
Definition: A general term for the complete or partial loss of the ability to hear from one or both ears.
Definition Source(s): MESH:D034381
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: Hearing impairmentPMID:22246673 PMID:23235333 PMID:25741868 PMID:28492532 PMID:30311386
CLDN14-AS1 IAGP (Homo sapiens) or (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Hearing impairment | ClinVar Annotator: match by term: Nonsyndromic Hearing Loss, RecessivePMID:30311386
CLDN14-AS1 IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Hearing impairmentPMID:22246673 PMID:23235333 PMID:28492532 PMID:30311386
CLDN14-AS1 IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Hearing impairmentPMID:25741868 PMID:28492532 PMID:30311386
CLDN14-AS1 IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Nonsyndromic Hearing Loss, RecessivePMID:11163249 PMID:15880785 PMID:22246673 PMID:25741868 PMID:30303587
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