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GENE - TERM ANNOTATION REPORT

CRRD ID: 14124682
Species: Sus scrofa
CRRD Object: Gene
Symbol: KIF7
Name: kinesin family member 7
Acc ID: DOID:3827
Term: congenital diaphragmatic hernia
Definition: A diaphragm disease characterized by the lack of development of all or part of the diaphragm, which results in an abnormal opening that allows the stomach and intestines to move into the chest cavity and crowd the heart and lungs. (DO)
Definition Source(s): http://en.wikipedia.org/wiki/Congenital_diaphragmatic_hernia "DO", http://ghr.nlm.nih.gov/condition/congenital-diaphragmatic-hernia "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)
KIF7 ISORGD:13103109068941CRRDmRNA, protein:decreased expression:diaphragmatic mesenchyme, pulmonary mesenchyme,

PMID:25921351, REF_RGD_ID:11553839
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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.