Submit Data |  Help |  Video Tutorials |  News |  Publications |  FTP Download |  REST API |  Citing RGD |  Contact   

GENE - TERM ANNOTATION REPORT

RGD ID: 9022945
Species: Chinchilla lanigera
RGD Object: Gene
Symbol: Fkbp14
Name: FKBP prolyl isomerase 14
Acc ID: DOID:630
Term: genetic disease
Definition: Diseases that are caused by genetic mutations present during embryo or fetal development, although they may be observed later in life. The mutations may be inherited from a parent's genome or they may be acquired in utero.
Definition Source(s): MESH:D030342, http://ghr.nlm.nih.gov/
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)
 ISSRGD:117443079068941ClinVarClinVar Annotator: match by term: Inborn genetic diseases

PMID:22265013, PMID:24677762, PMID:24773188, PMID:27149304, PMID:28492532
 ISSRGD:117443079068941ClinVarClinVar Annotator: match by term: Inborn genetic diseases

PMID:22265013, PMID:24677762, PMID:24773188, PMID:27149304, PMID:28492532, PMID:28617417, PMID:31132235
Go Back to source page   Continue to Ontology report

NHLBI Logo

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