Terminology Service < Semantic Lookup Platform

All terms in DOID

Label	Id	Description
spermatogenic failure 22	DOID_0070177	[An azoospermia characterized by autosomal recessive inheritance of spermatocyte maturation arrest resulting in azoospermia that has_material_basis_in mutation in the MEIOB gene on chromosome 16p13.]
retrogene	SO_0001219
spermatogenic failure 17	DOID_0070174	[A male infertility characterized by autosomal recessive inheritance of oocyte activation failure following intracytoplasmic sperm injection that has_material_basis_in mutation in the PLCZ1 gene on chromosome 12p12.]
transgenic_insertion	SO_0001218	[An insertion that derives from another organism, via the use of recombinant DNA technology.]
insertion	SO_0000667	[The sequence of one or more nucleotides added between two adjacent nucleotides in the sequence.]
obsolete spermatogenic failure 9	DOID_0070175
protein_coding_gene	SO_0001217
spermatogenic failure 15	DOID_0070172	[An azoospermia characterized by autosomal recessive inheritance of azoospermia that has_material_basis_in mutation in the SYCE1 gene on chromosome 10q26.]
endonuclease_spliced_intron	SO_0001216	[An intron that spliced via endonucleolytic cleavage and ligation rather than transesterification.]
intron	SO_0000188	[A region of a primary transcript that is transcribed, but removed from within the transcript by splicing together the sequences (exons) on either side of it.]
spermatogenic failure 7	DOID_0070173	[A male infertility characterized by autosomal recessive inheritance of impaired or absent sperm motility and increased incidence of morphologically abnormal sperm that has_material_basis_in mutation in the CATSPER1 gene on chromosome 11q13.]
coding_region_of_exon	SO_0001215	[The region of an exon that encodes for protein sequence.]
exon_region	SO_0000852	[A region of an exon.]
spermatogenic failure 19	DOID_0070170	[A male infertility characterized by autosomal recessive inheritance of sperm flagellar morphological abnormalities that has_material_basis_in mutation in the CFAP43 gene on chromosome 10q25.]
noncoding_region_of_exon	SO_0001214	[The maximal intersection of exon and UTR.]
spermatogenic failure 12	DOID_0070171	[A male infertility characterized by autosomal dominant inheritance of azoospermia or severe oligoasthenoteratozoospermia and in some cases a Sertolic cell-only phenotype that has_material_basis_in heterozygous mutation in the NANOS1 gene on chromosome 10q26.]
group_III_intron	SO_0001213	[Group III introns are introns found in the mRNA of the plastids of euglenoid protists. They are spliced by a two step transesterification with bulged adenosine as initiating nucleophile.]
autocatalytically_spliced_intron	SO_0000588	[A self spliced intron.]
silenced_by_histone_deacetylation	SO_0001223	[An attribute describing an epigenetic process where a gene is inactivated by histone deacetylation.]
silenced_by_histone_modification	SO_0001221	[An attribute describing an epigenetic process where a gene is inactivated by histone modification.]