Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Pivot Concepts:
Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Target Concepts:
Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Query: UMLS:C0022104 (
irritable bowel syndrome
)
8,033
document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)
Very early onset inflammatory bowel disease (VEOIBD) denotes children with onset of
IBD
before six years of age. A number of monogenic disorders are associated with VEOIBD including
tetratricopeptide repeat domain 7A
(
TTC7A
) deficiency.
TTC7A
-deficiency is characterized by apoptotic colitis in milder cases with severe intestinal atresia and immunodeficiency in cases with complete loss of protein. We used whole exome sequencing in a VEOIBD patient presenting with colitis characterized by colonic apoptosis and no identified known VEOIBD variants, to identify compound heterozygous deleterious variants in the Ubiquitin protein ligase E3 component N-recognin 5 (UBR5) gene. Functional studies demonstrated that UBR5 co-immunoprecipitates with the
TTC7A
and the UBR5 variants had reduced interaction between UBR5 and
TTC7A
. Together this implicates UBR5 in regulating
TTC7A
signaling in VEOIBD patients with apoptotic colitis.
...
PMID:The E3 ubiquitin ligase UBR5 interacts with TTC7A and may be associated with very early onset inflammatory bowel disease. 3312 18