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GENE - TERM ANNOTATION REPORT

RGD ID: 621351
Species: Rattus norvegicus
RGD Object: Gene
Symbol: Col1a2
Name: collagen type I alpha 2 chain
Acc ID: DOID:0110341
Term: osteogenesis imperfecta type 2
Definition: An osteogenesis imperfecta that is characterized by bone fragility and perinatal lethality and has_material_basis_in dominantly inherited mutations in the COL1A1 gene on chromosome 17q21.33 or the COL1A2 gene on chromosome 7q21.3. (DO)
Definition Source(s): https://www.ncbi.nlm.nih.gov/pubmed/3722184, https://www.ncbi.nlm.nih.gov/pubmed/6304100
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.
QualifierEvidenceWithReferenceSourceNotesOriginal Reference(s)
 ISORGD:7309847240710OMIM  
 ISORGD:7309848554872ClinVarClinVar Annotator: match by OMIM:166210

 
 ISORGD:7309848554872ClinVarClinVar Annotator: match by OMIM:166210

PMID:1301191
 ISORGD:7309848554872ClinVarClinVar Annotator: match by OMIM:166210

PMID:1711048
 ISORGD:7309848554872ClinVarClinVar Annotator: match by OMIM:166210

PMID:1874719
 ISORGD:7309848554872ClinVarClinVar Annotator: match by OMIM:166210

PMID:25741868, PMID:26938784
 ISORGD:7309848554872ClinVarClinVar Annotator: match by OMIM:166210

PMID:2777764
 ISORGD:7309848554872ClinVarClinVar Annotator: match by OMIM:166210

PMID:2839839
 ISORGD:7309848554872ClinVarClinVar Annotator: match by OMIM:166210

PMID:2914942
 ISORGD:7309848554872ClinVarClinVar Annotator: match by OMIM:166210

PMID:7959683
 ISORGD:7309848554872ClinVarClinVar Annotator: match by OMIM:166210

PMID:9923651
 ISORGD:7309848554872ClinVarClinVar Annotator: match by term: OI, TYPE II

PMID:25741868, PMID:28492532
 ISORGD:7309848554872ClinVarClinVar Annotator: match by term: Osteogenesis Imperfecta Type IIA

PMID:16705691, PMID:17078022, PMID:19344236, PMID:22589248, PMID:25326637, PMID:25450603, PMID:25741868, PMID:25944380, PMID:27519266, PMID:28492532, PMID:7695699, PMID:8094076, PMID:8218237, PMID:9016532
 ISORGD:7309848554872ClinVarClinVar Annotator: match by term: Osteogenesis Imperfecta Type IIA

PMID:16786509, PMID:25741868, PMID:28492532
 ISORGD:7309848554872ClinVarClinVar Annotator: match by term: Osteogenesis Imperfecta Type IIA

PMID:17078022, PMID:19344236, PMID:25741868, PMID:28492532, PMID:7695699, PMID:8218237, PMID:9016532
 ISORGD:7309848554872ClinVarClinVar Annotator: match by term: Osteogenesis Imperfecta Type IIA

PMID:17078022, PMID:22589248, PMID:25741868, PMID:28492532, PMID:7860070, PMID:9272740
 ISORGD:7309848554872ClinVarClinVar Annotator: match by term: Osteogenesis Imperfecta Type IIA

PMID:21520333, PMID:25741868, PMID:25944380, PMID:28492532
 ISORGD:7309848554872ClinVarClinVar Annotator: match by term: Osteogenesis Imperfecta Type IIA

PMID:25326637, PMID:28492532
 ISORGD:7309848554872ClinVarClinVar Annotator: match by term: Osteogenesis Imperfecta Type IIA

PMID:25741868, PMID:26604951, PMID:28492532
 ISORGD:7309848554872ClinVarClinVar Annotator: match by term: Osteogenesis Imperfecta Type IIA

PMID:28492532
 ISORGD:7309848554872ClinVarClinVar Annotator: match by term: OSTEOGENESIS IMPERFECTA, TYPE II

PMID:1385413
 ISORGD:7309848554872ClinVarClinVar Annotator: match by term: OSTEOGENESIS IMPERFECTA, TYPE II

PMID:3372533
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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.