Terminology Service < Semantic Lookup Platform

All terms in NCIT

Label	Id	Description
Insulin-Degrading Enzyme	NCIT_C112878	[Insulin-degrading enzyme (1019 aa, ~118 kDa) is encoded by the human IDE gene. This protein is involved in the metabolism of bioactive peptides.]
PEG3 wt Allele	NCIT_C112871	[Human PEG3 wild-type allele is located in the vicinity of 19q13.4 and is approximately 31 kb in length. This allele, which encodes paternally-expressed gene 3 protein, plays a role in both apoptosis and tumor suppression.]
PEG3 Gene	NCIT_C112870	[This gene is involved in both tumor suppression and apoptosis.]
19q13.4	NCIT_C24986	[A chromosome band present on 19q]
Paternally-Expressed Gene 3 Protein	NCIT_C112872	[Paternally-expressed gene 3 protein (1588 aa, ~181 kDa) is encoded by the human PEG3 gene. This protein is involved in both tumor suppression and the regulation of apoptosis.]
Protein Activation Pathway	NCIT_C40420	[A sequence of biological or biochemical events that are involved in the manifestation of the activity of a protein.]
Regulatory Pathway	NCIT_C19779	[An elaboration of the known or inferred interactions controlling the expression of a product.]
DCN Gene	NCIT_C112873	[This gene plays a role in proteoglycan synthesis.]
Protein Cycling Pathway	NCIT_C40421	[A representation of the sequence of biological or biochemical events that occur as a protein is cycled between the plasma membrane and endosomal vesicles.]
Transport Pathway	NCIT_C91760	[An elaboration of the sequence of biological or biochemical events that result in the transport of molecules from one physiological space to another.]
DCN wt Allele	NCIT_C112874	[Human DCN wild-type allele is located in the vicinity of 12q21.33 and is approximately 38 kb in length. This allele, which encodes decorin protein, is involved in extracellular matrix collagen fibril formation. A genetic deletion in this gene is associated with congenital stromal corneal dystrophy.]
TGF-beta Signaling Pathway KEGG	NCIT_C91522
Other Biochemical Pathway	NCIT_C40422
Brain Hamartoma	NCIT_C40423	[A hamartoma that occurs in the brain.]
Non-Neoplastic Brain Disorder	NCIT_C97154	[A non-neoplastic disorder that affects the brain. Representative examples include cerebrovascular disorder, hydrocephalus, and encephalitis.]
Central Nervous System Hamartoma	NCIT_C5509	[A hamartoma that occurs in the central nervous system.]
Cartilaginous Hamartoma	NCIT_C40424	[A hamartoma characterized by the presence of cartilaginous elements.]
Congenital Hamartoma	NCIT_C40425	[A hamartomatous lesion which is present at birth.]
Imprinting Gene	NCIT_C54401	[A gene that does not exhibit equal expression of both alleles due to repression or inactivation, resulting in the genetic non-equivalence of mammalian paternal and maternal genomes.]
Monoclonal Antibody Therapy	NCIT_C15490	[The use of monoclonal antibodies in the treatment of any disease or disorder.]