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GENE - TERM ANNOTATION REPORT

RGD ID: 18927912
Species: Heterocephalus glaber
RGD Object: Gene
Symbol: Myo7a
Name: myosin VIIA
Acc ID: DOID:0050565
Term: autosomal recessive nonsyndromic deafness
Definition: A nonsyndromic deafness characterized by an autosomal recessive inheritance mode. (DO)
Definition Source(s): http://ghr.nlm.nih.gov/condition/nonsyndromic-deafness "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)
Myo7a ISOMYO7A (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Autosomal recessive nonsyndromic deafness | ClinVar Annotator: match by term: Deafness, autosomal recessivePMID:10094549 PMID:10425080 PMID:10447383 PMID:10930322 PMID:12112664 PMID:15043528 PMID:16470552 PMID:16652077 PMID:16679490 PMID:16963483 PMID:18181211 PMID:19074810 PMID:20052763 PMID:21311020 PMID:21436283 PMID:21569298 PMID:21873662 PMID:22135276 PMID:22898263 PMID:23451239 PMID:23591405 PMID:23770805 PMID:24033266 PMID:24194196 PMID:25404053 PMID:25425308 PMID:25468891 PMID:25558175 PMID:25741868 PMID:25798947 PMID:26226137 PMID:26791358 PMID:27344577 PMID:27460420 PMID:27573290 PMID:27957503 PMID:28041643 PMID:28492532 PMID:29692870 PMID:30303587 PMID:30311386 PMID:30459346 PMID:30718709 PMID:31479088 PMID:33089500 PMID:33187236 PMID:33269433 PMID:33671976 PMID:36147510 PMID:36909829 PMID:38189974 PMID:8900236
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