GENE - TERM ANNOTATION REPORT
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 Symbol | Qualifier | Evidence | With | Reference | Source | Notes | Original Reference(s) | C3 | | IAGP | (Homo sapiens) | 8554872 | ClinVar | ClinVar Annotator: match by term: Inborn genetic diseases | PMID:25741868 PMID:28492532 | C3 | | IAGP | (Homo sapiens) | 8554872 | ClinVar | ClinVar Annotator: match by term: Inborn genetic diseases | PMID:28492532 | C3 | | IAGP | (Homo sapiens) | 8554872 | ClinVar | ClinVar Annotator: match by term: Inborn genetic diseases | PMID:28492532 | C3 | | IAGP | (Homo sapiens) | 8554872 | ClinVar | ClinVar Annotator: match by term: Inborn genetic diseases | | C3 | | IAGP | (Homo sapiens) | 8554872 | ClinVar | ClinVar Annotator: match by term: Inborn genetic diseases | | C3 | | IAGP | (Homo sapiens) | 8554872 | ClinVar | ClinVar Annotator: match by term: Inborn genetic diseases | PMID:28492532 | C3 | | IAGP | (Homo sapiens) | 8554872 | ClinVar | ClinVar Annotator: match by term: Inborn genetic diseases | | C3 | | IAGP | (Homo sapiens) | 8554872 | ClinVar | ClinVar Annotator: match by term: Inborn genetic diseases | | C3 | | IAGP | (Homo sapiens) | 8554872 | ClinVar | ClinVar Annotator: match by term: Inborn genetic diseases | PMID:28492532 | C3 | | IAGP | (Homo sapiens) | 8554872 | ClinVar | ClinVar Annotator: match by term: Inborn genetic diseases | | C3 | | IAGP | (Homo sapiens) | 8554872 | ClinVar | ClinVar Annotator: match by term: Inborn genetic diseases | | C3 | | IAGP | (Homo sapiens) | 8554872 | ClinVar | ClinVar Annotator: match by term: Inborn genetic diseases | | C3 | | IAGP | (Homo sapiens) | 8554872 | ClinVar | ClinVar Annotator: match by term: Inborn genetic diseases | PMID:28492532 | C3 | | IAGP | (Homo sapiens) | 8554872 | ClinVar | ClinVar Annotator: match by term: Inborn genetic diseases | PMID:28492532 | C3 | | IAGP | (Homo sapiens) | 8554872 | ClinVar | ClinVar Annotator: match by term: Inborn genetic diseases | | C3 | | IAGP | (Homo sapiens) | 8554872 | ClinVar | ClinVar Annotator: match by term: Inborn genetic diseases | | C3 | | IAGP | (Homo sapiens) | 8554872 | ClinVar | ClinVar Annotator: match by term: Inborn genetic diseases | | C3 | | IAGP | (Homo sapiens) | 8554872 | ClinVar | ClinVar Annotator: match by term: Inborn genetic diseases | | C3 | | IAGP | (Homo sapiens) | 8554872 | ClinVar | ClinVar Annotator: match by term: Inborn genetic diseases | | C3 | | IAGP | (Homo sapiens) | 8554872 | ClinVar | ClinVar Annotator: match by term: Inborn genetic diseases | PMID:16687714 PMID:17634448 PMID:17767156 PMID:19259132 PMID:1976733 PMID:20664795 PMID:21576320 PMID:22718507 PMID:23112567 PMID:23455636 PMID:25741868 PMID:28492532 PMID:7870343 | C3 | | IAGP | (Homo sapiens) | 8554872 | ClinVar | ClinVar Annotator: match by term: Inborn genetic diseases | PMID:17634448 PMID:18325906 PMID:19168221 PMID:1976733 PMID:25741868 PMID:28492532 | |
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