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GENE - TERM ANNOTATION REPORT

RGD ID: 1323719
Species: Homo sapiens
RGD Object: Gene
Symbol: FAM20C
Name: FAM20C golgi associated secretory pathway kinase
Acc ID: DOID:10609
Term: rickets
Definition: A bone remodeling disease that has_material_basis_in impaired mineralization or calcification of bones before epiphyseal closure due to deficiency or impaired metabolism of vitamin D, phosphorus or calcium which results_in softening and deformity located_in bone. (DO)
Definition Source(s): http://en.wikipedia.org/wiki/Rickets "DO" "DO", http://www.mayoclinic.com/health/rickets/DS00813 "DO" "DO", http://www.nlm.nih.gov/medlineplus/ency/article/000344.htm "DO" "DO", http://www.umm.edu/ency/article/000344.htm "DO" "DO", https://en.wikipedia.org/wiki/Rickets#Types "DO" "DO", https://www.ncbi.nlm.nih.gov/pubmed/26365554 "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)
FAM20C ISSFam20c (Mus musculus)13592920MouseDOOMIM:264700 | OMIM:277440 | OMIM:600081 | OMIM:600785 
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