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GENE - TERM ANNOTATION REPORT

RGD ID: 155228627
Species: Homo sapiens
RGD Object: Gene
Symbol: LOC126862586
Name: CDK7 strongly-dependent group 2 enhancer GRCh37_chr17:48273702-48274901
Acc ID: DOID:9006782
Term: Combined Osteogenesis Imperfecta and Ehlers-Danlos Syndrome 1
Definition: null
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)
LOC126862586 IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: OIEDS SYNDROME 1PMID:12362985 PMID:17078022 PMID:19344236 PMID:21667357 PMID:22206639 PMID:23692737 PMID:25741868 PMID:25944380 PMID:26467025 PMID:26627451 PMID:27509835 PMID:27748872 PMID:28492532 PMID:31447884 PMID:7695699 PMID:8218237 PMID:8613526 PMID:9016532
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