Terminology Service < Semantic Lookup Platform

All terms in NCIT

Label	Id	Description
HMGB2 Gene	NCIT_C20579	[This gene is involved in cellular signaling, chromatin remodeling, and regulation of gene transcription.]
HMGN Family Gene	NCIT_C20575	[Human HMGN Family Genes encode nuclear HMGN proteins that bind to nucleosomes, change chromatin architecture, and enhance transcription or replication. They typically contain a Nucleosome Binding Domain that anchors these proteins to nucleosome cores to facilitate changes in higher order chromatin structure. HMGN chromatin association is dynamic and regulated by posttranslational modification; related to cell cycle and transcriptional events. (NCI)]
HMGA1 Gene	NCIT_C20576	[This gene plays a role in a number of cellular processes including apoptosis, chromatin organization and transcriptional regulation.]
HMGA2 Gene	NCIT_C20577	[This gene is involved in chromatin organization and regulation of gene transcription. It also plays a role in development.]
Conventional Lipoma	NCIT_C27530	[A benign well-circumscribed tumor, composed of lobules of mature adipocytes, that arises within subcutaneous tissue, deep soft tissues or on the surface of bones.]
CDISC Questionnaire EPDS Test Name Terminology	NCIT_C132520	[Test names of questionnaire questions associated with the Edinburgh Postnatal Depression Scale (EPDS) for the Clinical Data Interchange Standards Consortium (CDISC) Study Data Tabulation Model (SDTM).]
HMGN1 Gene	NCIT_C20581	[This gene is involved in chromatin remodeling and enhancing gene transcription from chromatin templates.]
HMGN2 Gene	NCIT_C20582	[This gene plays a role in chromatin remodeling and enhancing gene transcription from chromatin templates.]
HMGN3 Gene	NCIT_C20583	[This gene is involved in chromatin remodeling and enhancing gene transcription from chromatin templates.]
HMGN4 Gene	NCIT_C20584	[This gene plays a role in chromatin remodeling and enhancing gene transcription from chromatin templates.]
HMGB3 Gene	NCIT_C20580	[This gene plays a role in development and the regulation of gene transcription.]
CDISC Questionnaire CES Test Name Terminology	NCIT_C132518	[Test names of questionnaire questions associated with the Combat Exposure Scale (CES) for the Clinical Data Interchange Standards Consortium (CDISC) Study Data Tabulation Model (SDTM).]
CDISC Questionnaire CES Test Code Terminology	NCIT_C132519	[Test codes of questionnaire questions associated with the Combat Exposure Scale (CES) for the Clinical Data Interchange Standards Consortium (CDISC) Study Data Tabulation Model (SDTM).]
Chromaffin Granule Amine Transporter	NCIT_C107580	[Chromaffin granule amine transporter (525 aa, ~56 kDa) is encoded by the human SLC18A1 gene. This protein is involved in the transport of biogenic monoamines into secretory vesicles.]
Fibroblast Growth Factor Receptor 2	NCIT_C17411	[Fibroblast growth factor receptor 2 (821 aa, ~92 kDa) is encoded by the human FGFR2 gene. This protein plays a role in heparin-dependent fibroblast growth factor signaling.]
IL10RA Gene	NCIT_C107582	[This gene plays a role in immunosuppression.]
FGFR2 NM_000141.4:c.755C>G	NCIT_C107583	[A nucleotide substitution at position 755 of the coding sequence of the FGFR2 gene where cytosine has been mutated to guanine.]
FGFR2 NP_000132.3:p.S252W	NCIT_C107585	[A change in the amino acid residue at position 252 in the fibroblast growth factor receptor 2 protein where serine has been replaced by tryptophan.]
IL10RA wt Allele	NCIT_C107584	[Human IL10RA wild-type allele is located in the vicinity of 11q23.3 and is approximately 15 kb in length. This allele, which encodes interleukin-10 receptor subunit alpha protein, is involved in the regulation of immunosuppression. Mutations in this gene are associated with inflammatory bowel disease 28, early onset, autosomal recessive.]
Interleukin-10 Receptor Subunit Alpha	NCIT_C107586	[Interleukin-10 receptor subunit alpha (578 aa, ~63 kDa) is encoded by the human IL10RA gene. This protein plays a role in the regulation of immunosuppression.]