Terminology Service < Semantic Lookup Platform

All terms in NCIT

Label	Id	Description
Worst Possible Tiredness	NCIT_C107393	[A question about an individual's experience of tiredness at its worst.]
Worst Possible Nausea	NCIT_C107394	[A question about an individual's experience of nausea at its worst.]
Worst Possible Depression	NCIT_C107395	[A question about an individual's experience of depression at its worst.]
GNAS NP_000507.1:p.R201C	NCIT_C146960	[A change in the amino acid residue at position 201 in the guanine nucleotide-binding protein G(s) subunit alpha isoforms short protein where arginine has been replaced by cysteine.]
GNAS NM_000516.5:c.601C>T	NCIT_C146959	[A nucleotide substitution at position 601 of the coding sequence of the GNAS gene where cytosine has been mutated to thymine.]
Worst Possible Anxiety	NCIT_C107396	[A question about an individual's experience of anxiety at its worst.]
GNAS NM_000516.5:c.601C>A	NCIT_C146961	[A nucleotide substitution at position 601 of the coding sequence of the GNAS gene where cytosine has been mutated to adenine.]
GNAS NP_000507.1:p.R201S	NCIT_C146962	[A change in the amino acid residue at position 201 in the guanine nucleotide-binding protein G(s) subunit alpha isoforms short protein where arginine has been replaced by serine.]
Feel Drowsy	NCIT_C107397	[A question about whether an individual feels or felt drowsy.]
Worst Possible Appetite	NCIT_C107398	[A question about an individual's appetite at its worst.]
Worst Possible Feeling of Overall Well-Being	NCIT_C107399	[A question about an individual's experience of overall well-being at its worst.]
RHBDF2 wt Allele	NCIT_C132323	[Human RHBDF2 wild-type allele is located in the vicinity of 17q25.3 and is approximately 31 kb in length. This allele, which encodes inactive rhomboid protein 2, is involved in the regulation of the secretion of various ligands of the epidermal growth factor receptor. Mutation of the gene is associated with tylosis with esophageal cancer.]
RHBDF2 Gene	NCIT_C132322	[This gene plays a role in modulation of epidermal growth factor receptor signaling pathways.]
17q25.3	NCIT_C24980	[A chromosome band present on 17q]
Monosialotetrahexosylganglioside	NCIT_C107389	[A glycosphingolipid containing a sialic acid residue found in neuronal cell membranes, with potential neuroprotective and neuroregenerative activities. Upon administration, monosialotetrahexosylganglioside, also called GM-1, is able to both prevent neurologic damage and induce regeneration of damaged neurons through neurotrophic repair mechanisms, enhancement of the production of neutrophins, and augmenting neurite outgrowth. In addition, GM-1 exerts anti-excitotoxic activity, prevents necrosis, and improves neuronal recovery and function.]
Inactive Rhomboid Protein 2	NCIT_C132324	[Inactive rhomboid protein 2 (856 aa, ~97 kDa) is encoded by the human RHBDF2 gene. This protein plays a role in the modulation of both epidermal growth factor receptor (EGFR) ligand secretion and EGFR-dependent signaling.]
PGAM1 Gene	NCIT_C132325	[This gene is involved in glycolysis.]
PGAM1 wt Allele	NCIT_C132326	[Human PGAM1 wild-type allele is located in the vicinity of 10q24.1 and is approximately 7 kb in length. This allele, which encodes phosphoglycerate mutase 1 protein, plays a role in the glycolytic pathway.]
Phosphoglycerate Mutase 1	NCIT_C132327	[Phosphoglycerate mutase 1 (254 aa, ~29 kDa) is encoded by the human PGAM1 gene. This protein is involved in the interconversion of 3- and 2-phosphoglycerate during glycolysis.]
Id Lymph Vaccine Test	NCIT_C29110	[A test consisting of a lymphoma idiotype (Id)-specific protein conjugated to the immunogen keyhole limpet hemocyanin (KLH). As a test of innate host delayed-type hypersensitivity (DTH) and host DTH in response to therapeutic vaccination, Id lymph vaccine test is performed intradermally before and after therapeutic vaccination in lymphoma patients treated with Id-specific vaccines. (NCI04)]