Terminology Service < Semantic Lookup Platform

All terms in NCIT

Label	Id	Description
CCL7 wt Allele	NCIT_C49750	[Human CCL7 wild-type allele is located within 17q11.2-q12 and is approximately 2 kb in length. This allele, which encodes C-C motif chemokine 7 protein, is involved in macrophage chemoattraction during inflammation and variants of the allele have been implicated in metastasis.]
CCL7 Gene	NCIT_C24786	[This gene plays a role in extracellular matrix modulation and inflammatory processes.]
CCL8 wt Allele	NCIT_C49751	[Human CCCL8 wild-type allele is located within 17q11.2 and is approximately 2 kb in length. This allele, which encodes C-C motif chemokine 8 protein, plays a role in the chemotaxis of monocytes, lymphocytes, basophils and eosinophils. The recruitment of leukocytes may contribute to tumor-associated leukocyte infiltration and to the antiviral state against HIV infection.]
CCL8 Gene	NCIT_C24787	[This gene is involved in the modulation of immune functions.]
CTF1 wt Allele	NCIT_C49752	[Human CTF1 wild-type allele is located within 16p11.2-p11.1 and is approximately 7 kb in length. This allele, which encodes cardiotrophin-1 protein, is involved in several signal transduction pathways.]
CTF1 Gene	NCIT_C24319	[This gene plays a role in signal transduction.]
GP5 Gene	NCIT_C126555	[This gene is involved in blood coagulation.]
GP5 wt Allele	NCIT_C126556	[Human GP5 wild-type allele is located in the vicinity of 3q29 and is approximately 4 kb in length. This allele, which encodes platelet glycoprotein V protein, plays a role in von Willebrand factor-dependent platelet aggregation.]
Platelet Glycoprotein V	NCIT_C126557	[Platelet glycoprotein V (560 aa, ~61 kDa) is encoded by the human GP5 gene. This protein is involved in von Willebrand factor binding.]
Combined Lipase Deficiency	NCIT_C126558	[A rare disorder caused by mutation in the LMF1 gene resulting in combined lipase deficiency with concomitant hypertriglyceridemia and associated disorders.]
LMF1 Gene	NCIT_C134605	[This gene plays a role in protein maturation.]
Platelet Membrane Glycoprotein 1b Beta Chain	NCIT_C126551	[Platelet glycoprotein Ib beta chain (206 aa, ~22 kDa) is encoded by the human GP1BB gene. This protein is involved in the modulation of platelet aggregation.]
GP9 Gene	NCIT_C126552	[This gene plays a role in von Willebrand factor binding.]
GP9 wt Allele	NCIT_C126553	[Human GP9 wild-type allele is located in the vicinity of 3q21.3 and is approximately 7 kb in length. This allele, which encodes platelet glycoprotein IX protein, is involved in the regulation of platelet aggregation. Mutation of the gene is associated with Bernard-Soulier syndrome type C.]
ECM-Receptor Interaction Signaling Pathway	NCIT_C91515
Hematopoietic Cell Lineage Pathway	NCIT_C91459
Platelet Glycoprotein IX	NCIT_C126554	[Platelet glycoprotein IX (177 aa, ~19 kDa) is encoded by the human GP9 gene. This protein plays a role in blood coagulation.]
Vaginal Itching	NCIT_C35112	[Itching of the skin of the vagina, vulva, and surrounding area.]
Genitourinary Signs and Symptoms	NCIT_C5035	[Patient complaints (symptoms), physical or laboratory findings (signs) related to the genitourinary system.]
Psychogenic Vaginismus	NCIT_C35113	[Involuntary spasm of the outer muscles of the vagina during penetration that results from a psychological cause.]