Terminology Service < Semantic Lookup Platform

All terms in NCIT

Label	Id	Description
FKBP5 wt Allele	NCIT_C105830	[Human FKBP5 wild-type allele is located in the vicinity of 6p21.31 and is approximately 155 kb in length. This allele, which encodes peptidyl-prolyl cis-trans isomerase FKBP5 protein, is involved in the modulation of protein folding.]
FKBP5 Gene	NCIT_C105829	[This gene plays a role in protein folding.]
Glucocorticoid Receptor Regulatory Network	NCIT_C91603
6p21.31	NCIT_C13795	[A chromosome band present on 6p]
Primordial Myocardium	NCIT_C34272	[A mass of splanchnic mesoderm enclosing the embryonic heart tube, which will become the muscular wall of the mature heart.]
Peptidyl-Prolyl Cis-Trans Isomerase FKBP5	NCIT_C105831	[Peptidyl-prolyl cis-trans isomerase FKBP5 (457 aa, ~51 kDa) is encoded by the human FKBP5 gene. This protein plays a role in the mediation of protein folding.]
Primordial Optic Nerve	NCIT_C34273	[The optic stalk, which is the constricted, proximal portion of the optic vesicles found in the embryo, and in which the lumen gradually obliterates as axons of ganglion cells accumulate in the inner layer and form the optic nerve.]
Embryonic Nervous System	NCIT_C34156	[The development of both the central and peripheral nervous systems, which begins during the third week of gestation.]
NEIL3 Gene	NCIT_C105832	[This gene plays a role in DNA repair.]
Primordial Phallus	NCIT_C34274	[The elongated genital tubercle that develops during the fourth week of gestation on the ventral side of the cloacal membrane, and which will give rise to either the glans penis or the clitoris.]
Embryonic Urogenital System	NCIT_C34059	[The development of the organs of both the urinary and reproductive systems from the intermediate mesoderm.]
NEIL3 wt Allele	NCIT_C105833	[Human NEIL3 wild-type allele is located in the vicinity of 4q34.3 and is approximately 53 kb in length. This allele, which encodes endonuclease 8-like 3 protein, is involved in DNA binding and repair.]
Base Excision Repair Pathway	NCIT_C91457
Primordium	NCIT_C34275	[The earliest recognizable stage of development of an anatomical structure, tissue, organ or cell.]
Embryo	NCIT_C28147	[An organism in its initial stage of development following fertilization. The human embryonic period lasts approximately eight weeks, during which time organogenesis takes place.]
Endonuclease 8-Like 3	NCIT_C105834	[Endonuclease 8-like 3 (605 aa, ~68 kDa) is encoded by the human NEIL3 gene. This protein plays a role in binding and repair of single-stranded DNA.]
ATP5F1E Gene	NCIT_C105835	[This gene is involved in ATP synthesis.]
ATP5F1E wt Allele	NCIT_C105836	[Human ATP5F1E wild-type allele is located in the vicinity of 20q13.32 and is approximately 7 kb in length. This allele, which encodes ATP synthase subunit epsilon, mitochondrial protein, plays a role in ATP biosynthesis. Mutation of the gene is associated with mitochondrial complex V (ATP synthase) deficiency nuclear type 3.]
Primordial Laryngeal Inlet	NCIT_C34270	[An opening between the laryngotracheal tube and the pharynx found in the early embryo, which will form to the definitive laryngeal inlet.]
Embryonic Respiratory System	NCIT_C34158	[The development of both the upper and lower respiratory tracts from the embryonic foregut endoderm and associated mesoderm, which begins during the fourth week of gestation.]