Preferred Name |
FGFR2 Gene |
|
Synonyms |
Fibroblast Growth Factor Receptor 2 Gene FGFR2 FGFR2 Gene |
|
Definitions |
This gene plays a role in mitogenesis and differentiation and mutations in the gene are associated with craniosynostotic syndromes and bone malformations. |
|
ID |
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C19931 |
|
code |
C19931 |
|
Concept_In_Subset |
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C157711 http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C142799 http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C142800 http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C116977 |
|
Contributing_Source |
CTRP GDC |
|
DEFINITION |
This gene plays a role in mitogenesis and differentiation and mutations in the gene are associated with craniosynostotic syndromes and bone malformations. |
|
Display_Name |
FGFR2 Gene |
|
FULL_SYN |
Fibroblast Growth Factor Receptor 2 Gene FGFR2 FGFR2 Gene |
|
HGNC_ID |
HGNC:3689 |
|
Is_Value_For_GDC_Property | ||
label |
FGFR2 Gene |
|
Legacy Concept Name |
FGFR2_Gene |
|
Maps_To |
FGFR2 |
|
OMIM_Number |
176943 |
|
Preferred_Name |
FGFR2 Gene |
|
prefixIRI |
Thesaurus:C19931 |
|
Semantic_Type |
Gene or Genome |
|
UMLS_CUI |
C1333542 |
|
subClassOf |
Delete | Mapping To | Ontology | Source |
---|---|---|---|
http://www.drugtargetontology.org/dto/DTO_03200150 | DTO | LOOM | |
http://purl.obolibrary.org/obo/NCIT_C19931 | BERO | LOOM | |
http://purl.bioontology.org/ontology/LNC/LP19704-3 | LOINC | LOOM |