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GENE - TERM ANNOTATION REPORT

RGD ID: 12718128
Species: Ictidomys tridecemlineatus
RGD Object: Gene
Symbol: LOC101972165
Name: myosin-7
Acc ID: DOID:630
Term: genetic disease
Definition: A disease that has_material_basis_in genetic variations in the human genome. (DO)
Definition Source(s): http://ghr.nlm.nih.gov/ "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)
LOC101972165 ISOMYH7 (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Inborn genetic diseasesPMID:10900182 PMID:11433818 PMID:12820698 PMID:12974739 PMID:14656445 PMID:15322983 PMID:15358028 PMID:15563892 PMID:16754800 PMID:17372140 PMID:17502101 PMID:17947214 PMID:18383048 PMID:19808347 PMID:19864899 PMID:199274 PMID:20031602 PMID:20624503 PMID:20733148 PMID:20800588 PMID:21252143 PMID:2136805 PMID:21499742 PMID:21511876 PMID:21839045 PMID:22455086 PMID:22763267 PMID:22765922 PMID:22918376 PMID:22958901 PMID:23281406 PMID:23299917 PMID:23349452 PMID:23396983 PMID:23426552 PMID:23707328 PMID:23711808 PMID:23861362 PMID:24033266 PMID:24055113 PMID:24093860 PMID:24111713 PMID:24119082 PMID:24503780 PMID:24510615 PMID:25086479 PMID:25125180 PMID:25163546 PMID:25351510 PMID:25524337 PMID:25666907 PMID:25741868 PMID:26246073 PMID:26332594 PMID:26743238 PMID:26914223 PMID:27532257 PMID:28193612 PMID:28265379 PMID:28408708 PMID:28416588 PMID:28492532 PMID:28615295 PMID:28771489 PMID:28807990 PMID:28971120 PMID:29300372 PMID:29915098 PMID:30588760 PMID:30775854 PMID:31006259 PMID:3203908 PMID:32344918 PMID:32894683 PMID:33309763 PMID:33495596 PMID:33495597 PMID:33673806 PMID:34542152 PMID:34598319 PMID:35653365 PMID:7883988 PMID:7909436 PMID:8533830 PMID:8614836 PMID:8981935 PMID:9884344
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